- Open Access
Cariporide and other new and powerful NHE1 inhibitors as potentially selective anticancer drugs – an integral molecular/biochemical/metabolic/clinical approach after one hundred years of cancer research
- Salvador Harguindey†1Email author,
- Jose Luis Arranz1,
- Julian David Polo Orozco1,
- Cyril Rauch2,
- Stefano Fais3, 4,
- Rosa Angela Cardone5 and
- Stephan J Reshkin†5
© Harguindey et al.; licensee BioMed Central Ltd. 2013
- Received: 21 May 2013
- Accepted: 25 October 2013
- Published: 6 November 2013
In recent years an increasing number of publications have emphasized the growing importance of hydrogen ion dynamics in modern cancer research, from etiopathogenesis and treatment. A proton [H+]-related mechanism underlying the initiation and progression of the neoplastic process has been recently described by different research groups as a new paradigm in which all cancer cells and tissues, regardless of their origin and genetic background, have a pivotal energetic and homeostatic disturbance of their metabolism that is completely different from all normal tissues: an aberrant regulation of hydrogen ion dynamics leading to a reversal of the pH gradient in cancer cells and tissues (↑pHi/↓pHe, or “proton reversal”). Tumor cells survive their hostile microenvironment due to membrane-bound proton pumps and transporters, and their main defensive strategy is to never allow internal acidification because that could lead to their death through apoptosis. In this context, one of the primary and best studied regulators of both pHi and pHe in tumors is the Na+/H+ exchanger isoform 1 (NHE1). An elevated NHE1 activity can be correlated with both an increase in cell pH and a decrease in the extracellular pH of tumors, and such proton reversal is associated with the origin, local growth, activation and further progression of the metastatic process. Consequently, NHE1 pharmaceutical inhibition by new and potent NHE1 inhibitors represents a potential and highly selective target in anticancer therapy. Cariporide, being one of the better studied specific and powerful NHE1 inhibitors, has proven to be well tolerated by humans in the cardiological context, however some side-effects, mainly related to drug accumulation and cerebrovascular complications were reported. Thus, cariporide could become a new, slightly toxic and effective anticancer agent in different human malignancies.
- pH and cancer
- Cancer etiopathogenesis
- Proton transporters
- Proton transport inhibitors
- Cariporide in cancer
- NHE1 and cancer
- Cancer treatment
- Multiple drug resistance
- New therapeutic paradigm in cancer
Proton transport and its inhibition as an approach to cancer etiopathogenesis and treatment
pH i and pH e in normal and cancer cells: apoptosis and antiapoptosis
( pH i < pH e )
( pH i > pH e )
(“proton gradient reversal”)
Intracellular pH (pH i )
interstitial pH (pH e )
pH i <6-6.5
Factors that increase cell pH and/or stimulate NHE activity as mediators of high pHi-mediated carcinogenicity
Virus (HPV E5, human polioma virus)
Oncogenes and viral proteins (v-mos, Ha-Ras, HPV16 E7)
Gen products (Bcl-2)
Chemicals carcinogens (arsenic salts, etc.)
Chronic hypoxia and HIF
Hormones (insulin, somatostatin, growth hormone, glucocorticoids)
Growth factors (IGF-1, HGH, PDGF, VEGF, EGF, IL-1, IL-8, TGF-β, G-CSF,
Angiotensin II, PGE2, diferric transferrin, bombesin)
Such an elevated pHi was very early on implicated as a crucial factor and target in neoplastic transformation in response to the overexpression of certain proton transporters as well as the ras and v-mos oncogenes [25, 26]. It was observed that oncogene-dependent transformation resulted in an elevated pHi, increased NHE1 activity and increased glycolysis, although it was not clear from those early experiments if the driving factor was the stimulated NHE1, an elevation of pHi or the increased glycolysis itself. This question was resolved in a study utilizing the inducible expression of an oncogene (HPV16 E7) to dissect the time-dependence of the appearance of the three above-mentioned factors . This study demonstrated that the first step in oncogene-dependent transformation of normal cells is the activation of the NHE1 with the subsequent cytosolic alkalinization followed by an increase in glycolysis. Furthermore, it was demonstrated that this alkalinization was the driver of a series of transformation hallmarks such as increased growth rate, substrate-independent growth, growth factor independence and tumor growth [4, 18, 27, 28]. Altogether, these data demonstrate that oncogenes utilize NHE1-induced cellular alkalinization to produce the unique cancer specific pH regulation with the resulting pH-related hallmark phenotypes characteristic of cancer cells. NHE1, by controlling pHi and preventing cell acidification plays a key role in cell survival/proliferation and tumour growth. Even from an epidemiological perspective, it was recently shown that low concentrations of arsenic salts in drinking water induce a carcinogenic effect directly related to the onset of different human tumors and that this effect is mediated by the stimulation of NHE1 and the resulting increase in cytosolic pH. These authors concluded that the increase in cell pH is an important pathogenetic mediator of the carcinogenic effects of arsenic salts , as has been reported in other parallel studies by different groups of researchers [4, 8–10, 13, 25, 28]. This is in line with previous reviews reporting a cause-effect relationship of a high microenvironmental pH and/or NHE stimulation with both pH-directly and pH-indirectly carcinogenesis, with the effects of a high pH reproducing most of the characteristics and metabolic behaviour of cancer cells .
Importantly, these complex dynamics of pH-metabolism engage the cell in a vicious cycle from very early on: the oncogene-driven alkalinization increases glycolysis and proliferation which, by generating a need for a high energy consumption, creates a high proton production that activates various proton efflux transport systems resulting in a further alkalinisation of the cell. This even further reduces oxidative phosporylation (OXPHOS) and increases glycolysis. This “chain-reaction” of deep-seated and dynamically disregulated H+ energetics creates a “perfect storm for cancer progression” . Finally, to our knowledge the pathological alkaline pHi of tumor cells and tissues have never been described in any other type of cell or disease other than malignancy [29, 30]. This adds further weight to the paradigm concerning the specificity and selectivity of these H+-mediated, deep-seated energetic abnormalities regarding the advantageous thermodynamics of the malignant process.
The pH of cancer cells and the Warburg Effect: a synthetic explanation
Similarities of effects of a high pH - Low [H + ] or (Alkalosis) and low pO 2 (Hypoxia) on cellular biochemistry and metabolism
(The Warburg effect)
Back to beginnings: a fatal historical error?
To understand the full significance of the most recent observations and data we need to go back in time to the beginnings of cancer biochemistry, and so, to the postulated origin of cancer cells [53, 54]. By doing so we realize that a fundamental confusion in the entire field of metabolic and biochemical cancer research was created from its very beginning. Nowadays, it is clear that Otto Warburg was wrong on the main point of his famous theory, namely, on the levels of cancer cell pHi, and consequently on its relationship to glycolysis. Indeed, Warburg believed that the pH of cancer cells was acid because of their high production rates of lactic acid [55–57]. Probably, the main reason for overlooking the true pH/glycolysis relationship, or at least for being given a secondary role at that time was that, during the 60’s and 70’s, the necessary technology to measure pHi was not available . The situation started to turn around just after Warburg’s death in 1970, when different reports began to emphasize that the pHi of cancer cells was the opposite from what was generally thought during Warburg’s life [18, 41, 43, 58]. Thus, Warburg could not have been aware that cellular alkalosis not only activates glycolysis but at the same time hinders oxidative phosphorylation and the entrance of pyruvate in the Krebs cycle [42, 59]. This allows a further insight into the reasons behind decades of confusion and disagreements on his theory of “the abnormal respiratory mechanisms of cancer cells”, that he defended all his life [8, 28, 42, 53, 59–61]. It is also important to remember that at Warburg’s time there were not techniques permitting the discrimination between the pH of the cytosol and of the internal organelles. Today we are able to show that within tumor cells the cytosol is alkaline while the cytoplasmic vesicles are very acidic [62, 63]. This is possible thanks to proton pumps, on one side eliminating protons outside the tumor cell when expressed on the plasma membrane, while pumping them from the cytosol to the internal lumen of the acidic vacuoles in order to avoid internal acidification (reviewed in ).
Importantly, any consideration concerning the intimate relationship of high pHi and glycolysis was fully missed during the famous arguments between Warburg and Weinhouse published in Science in 1956 [61, 62]. Indeed, all those heated discussions could only beg the real issue and could have been obviated if the true effect of pH on anaerobic and aerobic glycolysis and oxidative phosphorylation (“parahypoxia”)  could have been taken into account. Probably, this is also the main reason behind the fact that the search for the real cause underlying the Warburg effect has created many disagreements over the last decades [3, 56, 61, 63–71]. All in all, it can now be said that Warburg was right up to a certain point but that his critics were also partially right. However, all of them missed the main point. Aerobic glycolysis or damaged respiration was not the primary cause of cancer, as Warburg defended until his death. Indeed, the primary cause of cancer appears to be, precisely, the main cause of the aerobic glycolysis of tumors: a profound disruption of the homeostatic acid-balance of the cell mainly represented by an abnormally high pHi mediated by an extremely varied number of etiological factors of different natures. In summary, cellular alkalosis represents a common final pathway in cell transformation induced by a myriad of different stimuli, from oncogenes to virus to mitogens to growth factors and hormones to gene products [1, 4, 8–10, 27]. Finally, some recent and otherwise complete reviews dealing with Warburg’s contributions to modern concepts in cancer metabolism, tumor glycolysis, the initiation of cancer and oxidative phosphorylation have not considered the tight cause-effect interrelationships between pH and glycolysis, the Warburg effect and cancer proton reversal [65, 68, 69, 72, 73].
Anticancer potential of NHE inhibitors. Background to recent developments
Among them, the most important, functionally active, cancer-selective and better studied is the Na+/H+ exchanger isoform one, NHE1 [79–81]. The NHE1 is specifically involved in cellular acid–base balance and is the predominant isoform expressed in tumors, where it has been shown that it contributes to cellular pH homeostasis, cell transformation, proliferation, motility, migration, tumor growth, invasion, activation of the metastatic process, resistance to chemotherapy and probably also to the spontaneous regression of cancer [4, 31, 37, 82–84]. Conversely, decreasing NHE1 expression or inhibiting NHE1 activity leads to tumour cell growth arrest, inhibition of glycolysis, acidification of the intracellular space and selective apoptosis [29, 38, 45, 82]. An elevated NHE1 activity is considered to be the major factor in promoting tumor extracellular/interstitial acidity from even the earliest pre-cancer stage of oncogene-driven neoplastic transformation [25, 26]. However, large studies of patient cohort samples demonstrating that NHE1 is overexpressed in human tumors are lacking. Also, some cancer cells can be NHE1 negative and maintain cytosolic alkalinisation through expression of other MBPT [40, 85]. Consequently, NHE1 inhibitors appear predestined to be taken advantage of as a therapeutic target in probably most types of human cancer [81, 86–89]. For a detailed review of the structure and biophysical characteristics of NHE1, the regulation of the NHE1 activity and its role in tumor cells pH homeostasis, please refer to recent publications [2–4, 79, 80, 90].
Beyond studying in depth the evolution and progress of biochemical and metabolic cancer research, a major purpose of this review is to consider the fact that the new and selective NHE1 inhibitors show promise to become potent anticancer agents in preclinical trials and, eventually, in cancer patients. Amiloride was the first NHE inhibitor developed and it was shown to decrease vasoendothelial growth factor (VEGF) production and the activity of urokinase-type plasminogen activator (μPA), metalloproteinases (MMP) and other proteases, all of which aid in the activation of the metastatic process [89, 91–94]. Amiloride alone was shown to achieve a complete in vivo anti-metastatic effect in transplanted tumors in rats . Indeed, there are occasional reports of long-term treatment with amiloride in humans achieving remissions of cancer after chemotherapy had failed to control disease progression . Recent publications on the use of amiloride in cancer therapy discussed the different studies where its use had clear anti-neoplastic effects with few side-effects . Long before this, the utilization of amiloride and its derivatives were proposed as anticancer agents in bedside oncology . This potassium-sparing diuretic, apart from having a direct antitumoral, antimetastatic and antiangiogenic effect [95, 97, 98], at least in part by inhibiting uPA and VEGF, has been shown to be well tolerated and safe when used in the chronic situation in pharmacological dosages in humans, the main side-effect being occasionally increased plasma K+ levels [96, 99, 100]. Since more selective and powerful NHE inhibitors, like cariporide, are not available for human use, amiloride should still be part of new protocols dealing with the concerted use of a cocktail of proton transport inhibitors (PTIs) in different human solid tumors [5, 96, 101].
For many years investigators have waited for more specific and potent NHE inhibitors to be developed and be made available to the clinician . In this vein, powerful amiloride analogues, like ethylisopropylamiloride (EIPA), have been studied in different settings regarding its anticancer potential [103–105]. Hexamethylamiloride (HMA) and dimethylamiloride (DMA), were also introduced in basic experimental research and provided additional evidence of the validity of this approach. Striking results in different kinds of leukemic cells were reported with the potent NHE1 inhibitor HMA, which specifically decreases the pHi well below the survival threshold leading to selective apoptosis in a variety of human leukemic cells . This has led to the consideration that inducing a low pHi-mediated apoptosis as a cancer-specific therapeutic modality for all cancer cells and tissues could be a new and original approach to clinical therapeutics [27, 39, 44, 76, 106]. Regarding NHE-related malignant angiogenesis, the activity of a significant number of proangiogenic factors and oncogenes has been shown to positively affect NHE1 expression while, on the contrary, a wide array of anti-angiogenic drugs inhibit NHE1 [107, 108]. In summary, a great deal of evidence has been accumulating showing that the NHE is an important, and possibly selective, anticancer target [11, 81, 86, 87, 89, 100]. The pharmacology and therapeutic possibilities of the rest of the different proton transporters besides NHE1 have been thoroughly reviewed recently and will not be further dealt with here [4, 75, 81, 83].
Cariporide’s anticancer potential
Di Sario et al., have also shown that cariporide, through its selective inhibition of NHE1 and subsequent decrease of intracellular pH reduces proliferation and induces apoptosis in cholangiocarcinoma cells , leading these authors to suggest the potential therapeutic value of cariporide against this human tumor. A recent review has also focused on how to therapeutically target the NHE1-mediated metabolic transformations of cancer cells with cariporide . However, translation to the oncology clinic has yet to be realized because, unfortunately, the utilization of this drug in cancer treatment has not been explored [4, 84] and there is scarce data on NHE1 upregulation in tumour cells . This is most important since the concerted utilization of less potent and specific inhibitors of NHE1 and other proton transport inhibitors (PTIs) was recently advanced as a new, selective and integrated anticancer strategy [5, 101] (Figure 2).
The only non-amiloride based compounds with NHE1 inhibitory activity that have undergone clinical trials are cariporide and eniporide, and, unfortunately, those trials were not in the field of cancer but in a cardiological setting and for ischaemic-reperfusion injury. An early study on the effect of cariporide in 100 patients waiting to receive perfusion therapy via primary coronary angioplasty within 6 hours of the onset of symptoms suggested that reperfusion injury could be a target for NHE inhibitors and these results led to further clinical trials to confirm the therapeutic potential of NHE inhibitors . Two were with cariporide: The “Guard During Ischemia Against Necrosis” (Guardian) [114, 115] and “The Na+/H+ Exchanger Inhibition to Prevent Coronary Events in Acute Cardiac Conditions” (EXPEDITION) . The “Guardian” trial included a total of 11590 patients with unstable angina or a myocardial infarction who received placebo or different doses (30, 80 and 120 mg) of cariporide. There were an early clinical benefit and elevated six month survival rate in only a group of patients requiring urgent coronary bypass graft surgery and at a cariporide level of 120 mg. There was also a trial utilizing eniporide: “The Evaluation of the Safety and Cardioprotective Effects of Eniporide in Myocardial Infarction” (ESCAMI) .
Despite the cardioprotective value of cariporide in reducing myocardial infarcts in both the EXPEDITION and in the earlier GUARDIAN trials, use of the drug was associated in the EXPEDITION study with a significant increase in the rate of mortality (from 1.5% to 2.2% at day 5) due to an increase in cerebrovascular events [116, 118]. The appearance of these adverse effects in the last trial can probably be ascribed to the higher cumulating dose of cariporide administered in the EXPEDITION trial with respect to the GUARDIAN trial .
Clearly, a clinically reasonable initial approach in an oncology setting would be to minimize the systemic dose of the drug in order to dissociate the adverse and probably off-targets effects from the beneficial effects. Interestingly, rats having a lifelong treatment with cariporide had a greatly extended lifespan and this was interpreted as being due to a reduced occurrence of cancer . Finally, cariporide has been shown to be useful in overcoming multiple drug resistance (MDR) and the activity of the metastatic process . Besides, it is orally bioavailable and by this route of administration has been used but, unfortunately, never to date as an anticancer drug [114–119, 122–125]. Interestingly, hypoxia is part of the tumor metabolic microenvironment and has been shown to activate NHE1 and consequent invasion [109, 126, 127]. Cariporide reduces hypoxia-mediated tumor invasion of human tongue squamous cell carcinoma by inhibiting NHE1 . In this study, the authors demonstrated that inhibition of NHE1 by cariporide (HOE642) suppressed the invasion and migration of Tca8113 cells under hypoxic conditions. In another study pharmacological inhibition of p38 MAPK (mitogen-activated protein kinase) also significantly suppressed C/EBPα expression under hypoxia conditions after NHE1 inhibition . These results indicate the enhancement of hypoxia-induced K562 differentiation by NHE1 inhibition, which may be due to up-regulation of C/EBPα via p38 MAPK signalling pathway, which suggests a possible therapeutic target of NHE1 under hypoxia microenvironment in the treatment of leukaemic diseases. Finally, this also suggests that NHE1 inhibitors could be combined in clinical trials with antiangiogenics [129, 130] because tumor hypoxia and/or acidosis also stimulates VEGF [131, 132].
Indeed, in addition to VEGF release and, subsequently, neoangiogenesis, being stimulated by hypoxia, upregulation of VEGF has also been linked as being secondary to acidic pHe[131, 133]. Also, NHE1-dependent lowering in pHi also reduces the release of VEGF from the tumor cell so hindering motility and invasion [38, 134]. Systemic amiloride treatment also reduced experimentally-induced neovascularization in an animal model; probably through inhibition of NHE1 . For more detailed information please refer to the following review . Importantly, the potency of cariporide and some other NHE1 inhibitors is related to the ionization state of the guanidine residues. In this respect, the acidic extracellular pH of tumors (which can be as low as 6.2) will render zoniporide (pKa = 7.2), TY-12533 (pKa = 6.93) and, especially, cariporide (pKa = 6.28) positively charged. Therefore, the acidic tumor microenvironment could turn out to be an advantage in terms of dose-dependent side-effects as these compounds would be more efficient at inhibiting NHE1. Indeed, cariporide would be even more active at a very low pHe (ie. IC50 = 22 nM vs 120 nM at pHe 6.2 and 6.7, respectively) [136–138]. Finally, the development of new non-guanidine derived NHE1 inhibitors could alleviate some of the detrimental side-effects found in the Expedition trial (see section below on the new and potent non amiloride-derived and non guanidine-derived compounds).
The role of pH in multiple drug resistance (MDR)
Cariporide and other proton transport inhibitors in the overcoming of MDR
This H+-based “basic” approach to MDR-related cancer therapeutics may lead to more selectivity and less toxicity of other chemotherapeutic agents if used together with the most potent and selective PTIs known to date, like cariporide, Phx-3 or Compound 9 t [44, 81, 124]. Cariporide also increases the effect of gemcitabine in human cholangiocarcinoma cells by inhibiting MDR . Further along this line, the inhibition of the NHE1 has been shown to play a fundamental role in paclitaxel-induced apoptosis of breast cancer cells and this is synergistically potentiated by dimethyl amiloride (DMA) . This is reasonable since this counteracts the overexpression/ activation of the NHE1 which appears to contribute to the onset and/or maintenance of MDR [5, 81–83]. Thus, cariporide, because of its powerful effect in inhibiting NHE1, can also become a fundamental drug in overcoming MDR in human cancer therapy.
MDR, proton transport inhibitors (PTI), pH and P-glycoprotein (P-gp) In the same vein, De Milito et al. have shown that following PPI treatment of melanoma cells with esomeprazole overcomes MDR and undergo a significant decrease of proton gradient reversal, inducing tumor cell death via rapid intracellular acidification [153–155]. Also, the simultaneous inhibition of the NHE1 and H+-ATPase induces apoptosis through their concurrent effects on lowering pHi[147, 156, 157]. Finally, the relationships of NHE1 inhibition to tumor hypoxia, growth factors and antiangiogenic therapy have been extensively reviewed [10, 74, 158] and will not be further dealt with in this contribution. For detailed information on NHE/AntiNHE drug-relationships, please refer to the following original publication .
MDR and the cell membrane It is well known that the principal mechanism that regulates the entry of a drug into a cell is the existence of pH gradients between the extracellular environment and the intracellular compartments [170–175]. The reason why the pH gradient across the membrane is so important is related to its ability to ionize drug chemicals. While depending on the drugs, be it weak acid or weak base, it is generally agreed that ionized drugs - i.e. bearing a net positive charge due to local pH conditions, will be less prone to cross the bilayer membrane than non-ionized drugs because of their resulting ability to interact with other biological compounds. Normal tissues have a neutral extracellular/interstitial pH (pHe) whereas the intracellular pH (pHi) is slightly acidic. This should allow weakly basic drugs to enter passively into these cells. With weakly acid drugs it seems that the alkalinization of the cytosol of cancer cells can also impact on the lipid membrane by increasing the compaction of lipids making the membrane less permeable to chemicals independently of their ionization (see Figure 4) [82, 161, 173, 176, 177]. Since the increased interstitial acidity represents an advantage for the tumor to develop chemoresistance, using PTIs and/or PPIs will tend to normalize or even reverse the highly abnormal pH gradients in malignancy, leading to chemoresistance reversal.
These modifications of cancer H+ dynamics are associated with regression or delay of tumor growth and also with enhanced response to chemotherapy [154, 177–179]. It is suggested that the environmental conditions in tumors may allow the development of new and relatively specific therapies targeting the mechanisms regulating pHi under external acid conditions. Doxorubicin, cyclophosphamide, 5-fluorouracil, vincristine, vinblastine, mitoxantrone, daunorubicin and chlorambucil are all clinically useful drugs, which are ionisable and hence their distribution will be affected by the microenvironmental pHe [170, 173–175, 179]. In any case, protonation is not necessarily detrimental to drug-target interaction if the target displayed is extracellular (e.g. extracellular part of NHE1). In addition, the detrimental aspect of pH on drug-target interaction concerns weak bases only (e.g. doxorubicin). Cariporide is a weak acid (pKa ~ 4.5) and therefore protonation is beneficial as far as drug-target interaction is involved , and doi https://www.ebi.ac.uk/chembldb/index.php/compound/inspect/CHEMBL436559.
On the relationship of pHi, pHe and the NHE1 with tumor immunity
Marches et al. elegantly showed the intimate link between cancer biochemistry, molecular biology and immunity by demonstrating that the anti-IgM-mediated induction of cell death in human B lymphoma cells is dependent on NHE1 inhibition and subsequent intracellular acidification, up to a point unifying those fields under one wider embracing unit . In the same vein, it is accepted that the acid component of the tumor microenvironment directly impairs the function of the anti-tumoral immune system, thus contributing to the known in vivo immunosuppression by hindering a “host versus graft (the grafted malignant tumor)-like reaction”. Exposure to increasingly acidic pHe has also been shown to reduce tumor cell-induced cytolytic activity of lymphokine-activated killer (LAK) cells [182, 183], to play a role in down-regulating cytolytic activity of tumor-infiltrating lymphocytes with natural-killer (NK) phenotype  and to inhibit the non-major histocompatibility complex (MHC)-restricted cytotoxicity of immunocompetent effector cells [185–188]. Most recently, it has been proposed that tumour-secreted lactic acid represents a major mechanism by which cancers can suppress the anti-cancer immune response . This represents a further attempt to integrate different, so far separated fields, into larger and more all-comprehensive concepts , while at the same time introduces some fundamental MDR-related aspects of cancer immunity. It has also been recently shown that the NHE1, but not other isoforms, is an important mechanism in extruding H+ and regulating pHi in immune cells themselves, such as monocytes and neutrophils, that need NHE1 to be activated to maintain an optimal pHi for an effective immune defensive role .
From a therapeutic point of view, it has been shown that it is possible to alkalinize in vivo the interstitial component of malignant tumors with sodium bicarbonate or other different buffers  and that either acute or chronic treatment of tumor-bearing mice with sodium bicarbonate or proton pump inhibitors results in an increased antitumoral activity of different anti-tumor drugs . At the present time, preliminary preclinical and clinical trials are being conducted in order to overcome the anti-immune effects of the tumoral acid extracellular component when used together with immune-stimulating measures [191, 192]. A recent clinical study performed in companion animals with spontaneous tumors has shown a clear chemosensitization through a combination of high dosage proton pump inhibitors (PPIs) with different cytotoxic drugs and in tumors of different histology. This data provides a clinical proof of concept that inhibition of extracellular tumor microenvironment acidification through PPIs, PTIs and/or certain buffers may be considered a pivotal new approach in integral anticancer strategies [5, 147, 191–194]. This is a new and underdeveloped area that needs further research in the future.
New and potent non amiloride-derived and non guanidine-derived compounds (SL-591227, Phx-3, compound 9 t) as promising anticancer drugs
While amiloride and some of its first synthesized derivatives were non-selective and weak NHE inhibitors [195, 196], an additional series of NHE1 inhibitors whose structure is independent of amiloride have been later developed. SL-591227 was the first potent and NHE1 selective non-guanidine inhibitor [105, 113, 197]. The group of Tomoda developed two phenoxazine derivatives, Phx-1 and Phx-3 (for structures please see ref. ). Phx-3 is highly selective for NHE1 inhibition and was shown to selectively stimulate apoptosis in a variety of cancer cell lines while normal lymphocytes were not affected [44, 45]. Also, PHx-3 also effectively reversed a subcutaneously injected adult T-cell leukaemia tumor growth in animal studies without noticeable toxicity (A. Tomoda, personal communication). Otherwise, researchers at Bristol-Meyers synthesized a 5-aryl-4-(4-(5-methyl-1H-imidazol-4-yl)piperididn-1-yl)pyrimidine analog (compound 9 t) that was reported to have an excellent NHE1 inhibitory activity (IC50 = 0.0065 μM), to be 500-fold more potent against NHE1 than cariporide and to have much greater selectivity for NHE1 over NHE2 (1400-fold). Besides, compound 9 has a reported 52% oral bioavailability, a plasma half-life of 1.5 hours in rats, low side-effects in mice and may possess a significantly improved safety profile over other NHE1 inhibitors . Unfortunately, there have been no further publications utilizing this compound in any anticancer attempt either in vitro or in vivo.
On one hand, the development of the new non-guanidine derived NHE1 inhibitors could alleviate some of the detrimental effects of cariporide found in the EXPEDITION trial [116–118]. On the other hand, there are many reasons to think that there can be a significant selectivity of some of these NHE1 inhibitors in cancer (untested so far, at least clinically). In spite that NHE1 is ubiquitous and plays a fundamental role in pH housekeeping and volume control, it is also well known that in normal tissues the NHE1 is quiescent and is activated only during acidosis or cell shrinkage. Therefore, blocking it will have very little effect on the normal tissues. This should be an advantage to consider and exploit as an important degree of specificity in the anticancer effect of NHE1inhibitors, as it has been known from cell studies since the year 2000 [38, 44].
Towards a new and integral paradigm in human cancer therapeutics
Present and future prospects
The utilization of different PTIs in cancer therapeutics was originally suggested by the group of Pouysségur and our group as a novel approach to the pH-related treatment of malignant tumors because of its potential as a more selective and less toxic approach to therapeutics than conventional chemotherapy [5, 71, 129, 199]. We conducted a preliminary clinical trial with the concerted utilization of several PTIs [5, 101]. Pouysségur has also proposed the use of PTIs as a valid approach to cancer treatment, advancing that this 'pH-targeted’ therapy, perhaps combined with anti-angiogenesis in order to increase hypoxia-mediated acidosis, will synergistically induce the collapse and massive shrinkage of solid tumours . Similarly, from the therapeutic point of view, reverting the Warburg effect by selective intracellular acidification has been advanced as a treatment of cancer . Indeed, in the light of the older and the more recent contributions [4, 28, 44–46, 59] it can now be concluded that counteracting the Warburg effect and its aerobic glycolysis through any therapeutic method directed to selectively induce intracellular acidification in cancer cells and/or reverting proton reversal now appears to represent one and the same phenomenon.
In summary, the most potent and promising amiloride and non-amiloride derivatives, such as cariporide, Phx-3 and compound 9 t, etc. [37, 44, 113, 198] (see Figure 2) need to be included in pre-clinical and clinical trials as an important part of the anticancer armamentarium. That these compounds have not yet reached translational oncology becomes difficult to understand taking into account the massive theoretical background, available preclinical data as well as the results of the molecular, biochemical and metabolic studies already available at the present time. These anticancer compounds can be useful either as antitumoral and chemotherapeutic agents on their own, in the context of preventing and controlling the metastatic process and in any attempts to reverse MDR.
The effects of a targeted therapy are not durable when the therapy is designed to target a single biological molecule. This is because cellular pathways operate like webs with multiple redundancies or alternate routes that may be activated in response to the inhibition of a certain pathway. For this reason, combination and concerted therapies with PTIs will be often needed to effectively treat many tumors screened for pertinent pathway dependence. Incidentally, also in related fields like hyperthermia and radiation, it has also been known for a number of years that to keep the cytosolic pH at a certain level is fundamental as a survival mechanism, where cellular acidification increases the anticancer potential of both of these methods [187, 188], alone or in combination with NHE1 inhibitors. The most potent NHE1 inhibitors could be considered alone as chemotherapeutic agents since they are able to induce intracellular acidification and/or a reverse of the abnormal proton gradient of cancer cells and tissues. It can be advanced that they show a great promise as a new and selective approach to the treatment of a wide array of different malignant tumors and even leukaemias and, hopefully, they will help to overcome the present impasse and flat progress in cancer treatment [101, 200]. These strategies have been recently discussed in a review  and in a perspective  and introduce a real paradigm shift in cancer treatment.
Cell acid–base balance is recognized to be the main parameter to define cellular homeostasis, the life of cells being possible only within a very narrow range of pH (less that one unit). In that context, the pH of normal cells and cancer cells deviate towards opposite ends of a biological and metabolic spectrum. This energetic abnormality represents the largest difference among normal cellular physiology and cancer pathophysiology.
From an etiological and ethiopathogenic perpective, the hydrogen-related dynamics of malignancy have become a new approach to cancer that is helping to reach a better understanding of several, until now disparaged areas of cancer research both at basic and clinical levels, as well as of the intimate nature of the malignant disease. This unifying thermodynamic view permits an integration of different cancer fields, ranging from cell transformation and metabolism, local growth and invasion to neovascularisation and the activation and progression of the metastatic process (pH centric paradigm).
From a therapeutic perspective, the primary aim of this pH-based approach to cancer treatment is to manipulate the selective forces controlling the dysregulated pH dynamics of all cancer cells and tissues in order to regress tumor growth, control local invasion and deactivate the metastatic potential of malignant tumors within the same integral perspective and paradigm. All available evidence seems to indicate that this would take place regardless of pathological differences, tissue type or genetic origin. This therapeutic approach would also provide much less toxicity than present day treatments, probably more effective therapies than any other chemotherapy known to date and it has real possibilities to become a successful strategy in treating human cancer in general. A pathologically elevated pHi and its associated proton reversal (a reversed pH gradient in cancer cells and tissues (∆pHi to ∆pHe, ↑pHi/↓pHe) can be now considered a most specific cancer abnormality and essential hallmark of all kinds of malignant cells and tissues.
It can be concluded that aerobic glycolysis or damaged respiration was not the primary cause of cancer, as Warburg incorrectly defended until his death. It now seems more likely that the primary cause of cancer is, precisely, the main cause of the aerobic glycolysis of tumors. And this is that the abnormally high intracellular pH of cancer cells, mediated by a myriad of etiological factors of many different natures, can very well be the real cause of cancer. Furthermore, this tendency towards cellular alkalinity appears to be an specific and selective characteristic of cancer since it has not been described in any other disease.
This hydrogen ion-based perspective has also permitted the better understanding of the Warburg effect, which can now be simply explained by the effects of the concerted action of proton transporters in increasing intracellular pH and stimulating aerobic glycolysis. In this respect, Otto Warburg and his contemporaries committed an important historical error that has possibly misled several decades of metabolic and biochemical cancer research. The main limitation was probably imposed by the lack of available intracellular pH measurements before the time of Warburg’s death in 1970. The high pHi of tumor cells, the Warburg effect and the proton reversal of cancer cells and tissues are likely to represent one and the same phenomenon defined in different ways.
Many different environmental and chemical carcinogens have been shown to be cancer-inducing agents because of their potential to stimulate NHE1 activity with the subsequent increase in intracellular pH and decrease in microenvironmental pH. This cancer-inducing mechanism opens an entire new area in cancer epidemiology looking for generalizations both in detecting and controlling environmental carcinogens.
Any attempt to therapeutically induce a selective intracellular acidification using proton transport inhibitors (PTIs) in all cancer cells and tissues would secondarily increase interstitial tumoral pH, thus inhibiting the metastatic process, and represents a rational and firmly based approach to cancer treatment in all stages of development. Further, it has the potential of being selectively exploited in the treatment of many different malignant solid tumours.
Cariporide, other potent NHE1 inhibitors of the amiloride series, as well as powerful and selective NHE1 inhibitors of the non-amiloride series, like Phx-3 and compound 9 t, have the potential of being highly promising, minimally toxic and truly effective anticancer agents in a wide array of malignant tumours and leukaemias, hopefully representing a new paradigm in cancer therapeutics.
This work was supported by the Mercedes Castresana Foundation, Vitoria, Spain; the Association for Proton Cancer Research and Treatment (APCRT), Madrid, Spain; grant #11348 of the Italian Association for Cancer Research (l′AIRC), The Italian Ministry of Health, The University of Nottingham UK (NRF4305), the Medical Research Council UK (RA3804), PetPlan Charitable Trust UK (RB3858). We thank Jose Maria Bakero, Virginia Cuadrado, Iñigo Ruiz and the personnel of The Biotechnology Institute (BTI), Vitoria, Spain, for informatic help.
The authors want to apologize to all investigators who have significantly contributed to the different research fields reviewed here, past and present, but whose work is not specifically cited in this contribution.
*Note: Stefano Fais is the President and the rest of the authors are members of the International Society of Proton Dynamics in Cancer (ISPDC) (http://www.ispdc.eu). Salvador Harguindey is President of the Association for Proton Cancer Research and Treatment (APCRT), Madrid, Spain.
- Cardone RA, Casavola V, Reshkin SJ: The role of disturbed pH dynamics and the Na+/H+ exchanger in metastasis. Nat Rev Cancer. 2005, 5: 786-795. 10.1038/nrc1713.PubMedGoogle Scholar
- Webb BA, Chimenti M, Jacobson MP, Barber DL: Dysregulated pH: a perfect storm for cancer progression. Nat Rev Cancer. 2011, 11: 671-677. 10.1038/nrc3110.PubMedGoogle Scholar
- Neri D, Supuran CT: Interfering with pH regulation in tumours as a therapeutic strategy. Nat Rev Drug Discov. 2011, 10: 767-777. 10.1038/nrd3554.PubMedGoogle Scholar
- Reshkin SJ, Cardone RA, Harguindey S: Na+-H+ exchanger, pH regulation and cancer. Recent Pat Anticancer Drug Discov. 2013, 8: 85-99.PubMedGoogle Scholar
- Harguindey S, Arranz JL, Wahl ML, Orive G, Reshkin SJ: Proton transport inhibitors as potentially selective anticancer drugs. Anticancer Res. 2009, 29: 2127-2136.PubMedGoogle Scholar
- Brisson L, Reshkin SJ, Gore J, Roger S: pH regulators in invadosomal functioning: proton delivery for matrix tasting. Eur J Cell Biol. 2012, 91: 847-860. 10.1016/j.ejcb.2012.04.004.PubMedGoogle Scholar
- Brisson L, Gillet L, Calaghan S, Besson P, Le Guennec J, Roger S, Gore J: NaV1. 5 enhances breast cancer cell invasiveness by increasing NHE1-dependent H+ efflux in caveolae. Oncogene. 2010, 30: 2070-2076.PubMedGoogle Scholar
- Rubin H, Fodge D: Interrelationships of sugar transport and the initiation of DNA synthesisin chick embryo cells. Control of Proliferation of Animal Cells. Edited by: Clarkson B, Baserga R. 1974, New York: Cold Spring Harbor Laboratory, 801-816.Google Scholar
- Perona R, Serrano R: Increased pH and tumorigenicity of fibroblasts expressing a yeast proton pump. Nature. 1988, 334: 438-440. 10.1038/334438a0.PubMedGoogle Scholar
- Reshkin SJ, Bellizzi A, Caldeira S, Albarani V, Malanchi I, Poignee M, Alunni-Fabbroni M, Casavola V, Tommasino M: Na+/H+ exchanger-dependent intracellular alkalinization is an early event in malignant transformation and plays an essential role in the development of subsequent transformation-associated phenotypes. FASEB J. 2000, 14: 2185-2197. 10.1096/fj.00-0029com.PubMedGoogle Scholar
- Harguindey S, Pedraz JL, Garcia Canero R, Perez de Diego J, Cragoe EJ: Hydrogen ion-dependent oncogenesis and parallel new avenues to cancer prevention and treatment using a H(+)-mediated unifying approach: pH-related and pH-unrelated mechanisms. Crit Rev Oncog. 1995, 6: 1-33. 10.1615/CritRevOncog.v6.i1.20.PubMedGoogle Scholar
- Shimizu S, Eguchi Y, Kamiike W, Funahashi Y, Mignon A, Lacronique V, Matsuda H, Tsujimoto Y: Bcl-2 prevents apoptotic mitochondrial dysfunction by regulating proton flux. Proc Natl Acad Sci U S A. 1998, 95: 1455-1459. 10.1073/pnas.95.4.1455.PubMed CentralPubMedGoogle Scholar
- DiGiammarino EL, Lee AS, Cadwell C, Zhang W, Bothner B, Ribeiro RC, Zambetti G, Kriwacki RW: A novel mechanism of tumorigenesis involving pH-dependent destabilization of a mutant p53 tetramer. Nat Struct Biol. 2002, 9: 12-16. 10.1038/nsb730.PubMedGoogle Scholar
- Aravena C, Beltran AR, Cornejo M, Torres V, Diaz ES, Guzman-Gutierrez E, Pardo F, Leiva A, Sobrevia L, Ramirez MA: Potential role of sodium-proton exchangers in the low concentration arsenic trioxide-increased intracellular pH and cell proliferation. PLoS One. 2012, 7: e51451-10.1371/journal.pone.0051451.PubMed CentralPubMedGoogle Scholar
- Grinstein S, Rotin D, Mason MJ: Na+/H+ exchange and growth factor-induced cytosolic pH changes. Role in cellular proliferation. Bioch Biophys Acta. 1989, 988: 73-97. 10.1016/0304-4157(89)90004-X.Google Scholar
- Wakabayashi S, Fafournoux P, Sardet C, Pouysségur J: The Na+/H+ antiporter cytoplasmic domain mediates growth factor signals and controls “H(+)-sensing”. Proc Natl Acad Sci U S A. 1992, 89: 2424-2428. 10.1073/pnas.89.6.2424.PubMed CentralPubMedGoogle Scholar
- Sun I, Crane F, Löw H: Bombesin stimulates transplasma-membrane electron transport by Swiss 3 T3 cells. Biochim Biophys Acta (BBA)-Mol Cell Res. 1994, 1221: 206-210. 10.1016/0167-4889(94)90015-9.Google Scholar
- Eagle H: Some effects of environmental pH on cellular metabolism and function. Control of Proliferation in Animal Cells Cold Spring Harbor Conference on Cell Proliferation. 1974, New York: Cold Spring Harbor LaboratoryGoogle Scholar
- Moolenaar WH: Effects of growth factors on intracellular pH regulation. Annu Rev Plant Physiol Plant Mol Biol. 1986, 48: 363-376.Google Scholar
- Chiche J, Ilc K, Laferrière J, Trottier E, Dayan F, Mazure NM, Brahimi-Horn MC, Pouysségur J: Hypoxia-inducible carbonic anhydrase IX and XII promote tumor cell growth by counteracting acidosis through the regulation of the intracellular pH. Cancer Res. 2009, 69: 358-368. 10.1158/0008-5472.CAN-08-2470.PubMedGoogle Scholar
- Chiche J, Ricci JE, Pouysségur J: Tumor hypoxia and metabolism - towards novel anticancer approaches. Ann Endocrinol (Paris). 2013, 74 (2): 111-114. 10.1016/j.ando.2013.02.004.Google Scholar
- L’Allemain G, Paris S, Pouysségur J: Growth factor action and intracellular pH regulation in fibroblasts. Evidence for a major role of the Na+/H+ antiport. J Biol Chem. 1984, 259: 5809-5815.PubMedGoogle Scholar
- Pouysségur J, Franchi A, L’Allemain G, Paris S: Cytoplasmic pH, a key determinant of growth factor-induced DNA synthesis in quiescent fibroblasts. FEBS Lett. 1985, 190: 115-119. 10.1016/0014-5793(85)80439-7.PubMedGoogle Scholar
- Pouysségur J, Chambard JC, Franchi A, Paris S, Van Obberghen-Schilling E: Growth factor activation of an amiloride-sensitive Na+/H+ exchange system in quiescent fibroblasts: coupling to ribosomal protein S6 phosphorylation. Proc Natl Acad Sci U S A. 1982, 79: 3935-3939. 10.1073/pnas.79.13.3935.PubMed CentralPubMedGoogle Scholar
- Hagag N, Lacal JC, Graber M, Aaronson S, Viola MV: Microinjection of ras p21 induces a rapid rise in intracellular pH. Mol Cell Biol. 1987, 7: 1984-1988.PubMed CentralPubMedGoogle Scholar
- Doppler W, Jaggi R, Groner B: Induction of v-mos and activated Ha-ras oncogene expression in quiescent NIH 3 T3 cells causes intracellular alkalinisation and cell-cycle progression. Gene. 1987, 54: 147-153. 10.1016/0378-1119(87)90357-X.PubMedGoogle Scholar
- Harguindey S, Orive G, Luis Pedraz J, Paradiso A, Reshkin SJ: The role of pH dynamics and the Na+/H+ antiporter in the etiopathogenesis and treatment of cancer. Two faces of the same coin--one single nature. Biochim Biophys Acta Revs Cancer. 2005, 1756: 1-24. 10.1016/j.bbcan.2005.06.004.Google Scholar
- Lopez-Lazaro M: A new view of carcinogenesis and an alternative approach to cancer therapy. Mol Med. 2010, 16: 144-153.PubMed CentralPubMedGoogle Scholar
- Harguindey S, Orive G, Cacabelos R, Hevia EM, De Otazu RD, Arranz JL, Anitua E: An integral approach to the etiopathogenesis of human neurodegenerative diseases (HNDDs) and cancer. Possible therapeutic consequences within the frame of the trophic factor withdrawal syndrome (TFWS). Neuropsychiatr Dis Treat. 2008, 4: 1073-1084.PubMed CentralPubMedGoogle Scholar
- Harguindey S, Reshkin SJ, Orive G, Arranz JL, Anitua E: Growth and trophic factors, pH and the Na+/H+ exchanger in Alzheimer’s disease, other neurodegenerative diseases and cancer: new therapeutic possibilities and potential dangers. Curr Alzheimer Res. 2007, 4: 53-65. 10.2174/156720507779939841.PubMedGoogle Scholar
- Harguindey S, Cragoe EJ: The Na+/H+ antiporter in oncology in the light of the spontaneous regression of cancer and cell metabolism. Med Hypotheses. 1992, 39: 229-237. 10.1016/0306-9877(92)90114-R.PubMedGoogle Scholar
- Harguindey S: Integrating fields of cancer research through pivotal mechanisms and synthetic final pathways: a unifying and creative overview. Med Hypotheses. 2002, 58: 444-452. 10.1054/mehy.2001.1415.PubMedGoogle Scholar
- Gatenby RA, Gawlinski ET, Gmitro AF, Kaylor B, Gillies RJ: Acid-mediated tumor invasion: a multidisciplinary study. Cancer Res. 2006, 66: 5216-5223. 10.1158/0008-5472.CAN-05-4193.PubMedGoogle Scholar
- Lauritzen G, Stock CM, Lemaire J, Lund SF, Jensen MF, Damsgaard B, Petersen KS, Wiwel M, Ronnov-Jessen L, Schwab A, Pedersen SF: The Na+/H+ exchanger NHE1, but not the Na+, HCO3(-) cotransporter NBCn1, regulates motility of MCF7 breast cancer cells expressing constitutively active ErbB2. Cancer Lett. 2012, 317: 172-183. 10.1016/j.canlet.2011.11.023.PubMedGoogle Scholar
- Bhujwalla ZM, Artemov D, Ballesteros P, Cerdan S, Gillies RJ, Solaiyappan M: Combined vascular and extracellular pH imaging of solid tumors. NMR Biomed. 2002, 15: 114-119. 10.1002/nbm.743.PubMedGoogle Scholar
- Ludwig F, Schwab A, Stock C: The Na (+)/H(+)-exchanger (NHE1) generates pH nanodomains at focal adhesions. J Cell Physiol. 2012, 228 (6): 1351-1358.Google Scholar
- Amith SR, Fliegel L: Regulation of the Na+/H+ Exchanger (NHE1) in Breast Cancer Metastasis. Cancer Res. 2013, 73: 1259-1264. 10.1158/0008-5472.CAN-12-4031.PubMedGoogle Scholar
- Rich IN, Worthington-White D, Garden OA, Musk P: Apoptosis of leukemic cells accompanies reduction in intracellular pH after targeted inhibition of the Na(+)/H(+) exchanger. Blood. 2000, 95: 1427-1434.PubMedGoogle Scholar
- Porporato PE, Dhup S, Dadhich RK, Copetti T, Sonveaux P: Anticancer targets in the glycolytic metabolism of tumors: a comprehensive review. Front Pharmacol. 2011, 2: 49.PubMed CentralPubMedGoogle Scholar
- Parks S, Chiche J, Pouysségur J: Disrupting proton dynamics and energy metabolism for cancer therapy. Nat Cancer Revs. 2013, 13: 611-623. 10.1038/nrc3579.Google Scholar
- Kaminskas E: The pH-dependence of sugar-transport and glycolysis in cultured Ehrlich ascites-tumour cells. Biochem J. 1978, 174: 453-459.PubMed CentralPubMedGoogle Scholar
- Relman AS: Metabolic consequences of acid–base disorders. Kidney Int. 1972, 1: 347-359. 10.1038/ki.1972.46.PubMedGoogle Scholar
- Wilhelm G, Schulz J, Hofmann E: pH-dependence of aerobic glycolysis in ehrlich ascites tumour cells. FEBS Lett. 1971, 17: 158-10.1016/0014-5793(71)80587-2.PubMedGoogle Scholar
- Nagata H, Che XF, Miyazawa K, Tomoda A, Konishi M, Ubukata H, Tabuchi T: Rapid decrease of intracellular pH associated with inhibition of Na+/H+ exchanger precedes apoptotic events in the MNK45 and MNK74 gastric cancer cell lines treated with 2-aminophenoxazine-3-one. Oncol Rep. 2011, 25: 341-346.PubMedGoogle Scholar
- Che X-F, Zheng C-L, Akiyama S-I, Tomoda A: 2-Aminophenoxazine-3-one and 2-amino-4,4α-dihydro-4α,7-dimethyl-3H-phenoxazine-3-one cause cellular apoptosis by reducing higher intracellular pH in cancer cells. Proc Japan Acad, Series B Phys Biol Sci. 2011, 87: 199-213. 10.2183/pjab.87.199.Google Scholar
- Harguindey S, Henderson ES, Naeher C: Effects of systemic acidification of mice with Sarcoma 180. Cancer Res. 1979, 39: 4364-4371.PubMedGoogle Scholar
- Trivedi B, Danforth WH: Effect of pH on the kinetics of frog muscle phosphofructokinase. J Biol Chem. 1966, 241: 4110-4114.PubMedGoogle Scholar
- Gillies RJ: In vivo magnetic resonance spectroscopy in cancer. Annu Rev Biomed Eng. 2005, 7: 287-326. 10.1146/annurev.bioeng.7.060804.100411.PubMedGoogle Scholar
- Gallagher FA, Kettunen MI, Day SE, Hu DE, Ardenkjaer-Larsen JH, Zandt R, Jensen PR, Karlsson M, Golman K, Lerche MH, Brindle KM: Magnetic resonance imaging of pH in vivo using hyperpolarized 13C-labelled bicarbonate. Nature. 2008, 453: 940-943. 10.1038/nature07017.PubMedGoogle Scholar
- Gerweck LE, Seetharaman K: Cellular pH gradient in tumor versus normal tissue: potential exploitation for the treatment of cancer. Cancer Res. 1996, 56: 1194-1198.PubMedGoogle Scholar
- Lutz N, Le Fur Y, Chiche J, Pouysségur J, Cozzone P: Quantitative in-vivo characterization of intracellular and extracellular pH profiles in heterogeneous tumors: a novel method enabling multiparametric pH analysis. Cancer Res. 2013, 76: 4616-4628.Google Scholar
- Goldblatt H, Friedman L, Cechner R: On the malignant transformation of cells during prolonged culture under hypoxic conditions in vitro. Biochem Med. 1973, 7: 241-10.1016/0006-2944(73)90079-3.PubMedGoogle Scholar
- Warburg O: On the origin of cancer cells. Science. 1956, 123: 309-314. 10.1126/science.123.3191.309.PubMedGoogle Scholar
- Warburg O, Wind F, Negelein E: The metabolism of tumors in the body. J Gen Physiol. 1927, 8: 519-530. 10.1085/jgp.8.6.519.PubMed CentralPubMedGoogle Scholar
- Goldfeder A: Theoretical basis for the acidotic treatment of neoplasia. Am J Surg. 1933, 19: 307-312. 10.1016/S0002-9610(33)90435-3.Google Scholar
- Burk D: A Colloquial Consideration of the Pasteur and Neo-Pasteur Effects. Cold Spring Harb Symp Quant Biol. 1939, 7: 420-459. 10.1101/SQB.1939.007.01.034.Google Scholar
- Cori CF, Cori GT: The carbohydrate metabolism of tumors. I. The free sugar, lactic acid, and glycogen content of malignant tumors. J Biol Chem. 1925, 64: 11-22.Google Scholar
- Eagle H: The effect of environmental pH on the growth of normal and malignant cells. J Cell Physiol. 1973, 82: 1-8. 10.1002/jcp.1040820102.PubMedGoogle Scholar
- Calderon-Montano JSJ, Robles A, Lopez Lazaro M: Role of the Intracellular pH in the Metabolic Switch between Oxidative Phosphorylation and Aerobic Glycolysis - Relevance to Cancer. WebmedCentral CANCER. 2011, 2: 3-WMC001716Google Scholar
- Warburg O: The Nobel Lecture, June 1966. The Prime Cause and Prevention of Cancer. 1967, Würzburg, Germany: Konrad TriltschGoogle Scholar
- Warburg O: The Metabolism of Tumors. 1930, London: ConstableGoogle Scholar
- Weinhouse S: On respiratory impairment in cancer cells. Science. 1956, 124: 267-269. 10.1126/science.124.3215.267.PubMedGoogle Scholar
- Gatenby RA, Gillies RJ: Why do cancers have high aerobic glycolysis?. Nat Rev Cancer. 2004, 4: 891-899. 10.1038/nrc1478.PubMedGoogle Scholar
- Tennant DA, Duran RV, Gottlieb E: Targeting metabolic transformation for cancer therapy. Nat Rev Cancer. 2010, 10: 267-277. 10.1038/nrc2817.PubMedGoogle Scholar
- Ristow M: Oxidative metabolism in cancer growth. Curr Opin Clin Nutr Metab Care. 2006, 9: 339-345. 10.1097/01.mco.0000232892.43921.98.PubMedGoogle Scholar
- Moreno-Sanchez R, Rodriguez-Enriquez S, Marin-Hernandez A, Saavedra E: Energy metabolism in tumor cells. FEBS J. 2007, 274: 1393-1418. 10.1111/j.1742-4658.2007.05686.x.PubMedGoogle Scholar
- Koppenol WH, Bounds PL, Dang CV: Otto Warburg’s contributions to current concepts of cancer metabolism. Nat Rev Cancer. 2011, 11: 325-337. 10.1038/nrc3038.PubMedGoogle Scholar
- Hsu PP, Sabatini DM: Cancer cell metabolism: Warburg and beyond. Cell. 2008, 134: 703-707. 10.1016/j.cell.2008.08.021.PubMedGoogle Scholar
- Burk D, Woods M, Hunter J: On the significance of glucolysis for cancer growth, with special reference to Morris rat hepatomas. J Nat Cancer Inst. 1967, 38: 839-863.PubMedGoogle Scholar
- Kritikou E: Metabolism: Warburg effect revisited. Nature Rev Cancer. 2008, 8: 247-247.Google Scholar
- Kroemer G, Pouysségur J: Tumor cell metabolism: cancer’s Achilles’ heel. Cancer Cell. 2008, 13: 472-482. 10.1016/j.ccr.2008.05.005.PubMedGoogle Scholar
- Rietman EA, Friesen DE, Hahnfeldt P, Gatenby R, Hlatky L, Tuszynski JA: An integrated multidisciplinary model describing initiation of cancer and the Warburg hypothesis. Theoret Biol Med Model. 2013, 10: 39-10.1186/1742-4682-10-39. doi:10.1186/1742-4682-1110-1139Google Scholar
- Bailey KM, Wojtkowiak JW, Hashim AI, Gillies RJ: Targeting the metabolic microenvironment of tumors. Adv Pharmacol. 2012, 65: 63-107.PubMed CentralPubMedGoogle Scholar
- Parks S, Chiche J, Pouysségur J: pH control mechanisms of tumor survival and growth. J Cell Physiol. 2011, 226: 299-308. 10.1002/jcp.22400.PubMedGoogle Scholar
- Pedersen SF, Stock C: Ion Channels and Transporters in Cancer: Pathophysiology, Regulation, and Clinical Potential. Cancer Res. 2013, 73: 1658-1661. 10.1158/0008-5472.CAN-12-4188.PubMedGoogle Scholar
- Izumi H, Torigoe T, Ishiguchi H, Uramoto H, Yoshida Y, Tanabe M, Ise T, Murakami T, Yoshida T, Nomoto M, Kohno K: Cellular pH regulators: potentially promising molecular targets for cancer chemotherapy. Cancer Treat Revs. 2003, 29: 541-549. 10.1016/S0305-7372(03)00106-3.Google Scholar
- Moriyama Y, Nelson N: Inhibition of vacuolar H+-ATPases by fusidic acid and suramin. FEBS letters. 1988, 234: 383-10.1016/0014-5793(88)80121-2.PubMedGoogle Scholar
- Donowitz M, Tse CM, Fuster D: SLC9/NHE gene family, a plasma membrane and organellar family of Na+/H+ exchangers. Mol Aspects Med. 2013, 34: 236-251. 10.1016/j.mam.2012.05.001.PubMed CentralPubMedGoogle Scholar
- Boedtkjer E, Bunch L, Pedersen SF: Physiology, pharmacology and pathophysiology of the pH regulatory transport proteins NHE1 and NBCn1: similarities, differences, and implications for cancer therapy. Curr Pharm Des. 2012, 18: 1345-1371. 10.2174/138161212799504830.PubMedGoogle Scholar
- Stock C, Cardone RA, Busco G, Krahling H, Schwab A, Reshkin SJ: Protons extruded by NHE1: digestive or glue?. Eur J Cell Biol. 2008, 87: 591-599. 10.1016/j.ejcb.2008.01.007.PubMedGoogle Scholar
- Stock C, Ludwig FT, Schwab A: Is the multifunctional Na(+)/H(+) exchanger isoform 1 a potential therapeutic target in cancer?. Curr Med Chem. 2012, 19: 647-660. 10.2174/092986712798992101.PubMedGoogle Scholar
- Rauch C, Blanchard A, Wood E, Dillon E, Whal M, Harguindey S: Multiple Drug Resistance. Cell Membranes, Cytosolic pH and Drug Transport in Cancer and MDR: Physics, Biochemistry and Molecular Biology. Edited by: Meszaros A, Balogh G. 2009, New York: NovaGoogle Scholar
- Daniel C, Bell C, Burton C, Harguindey S, Reshkin SJ, Rauch C: The role of proton dynamics in the development and maintenance of multidrug resistance in cancer. Biochim Biophys Acta. 1832, 2013: 606-617.Google Scholar
- McLean LA, Roscoe J, Jørgensen NK, Gorin FA, Cala PM: Malignant gliomas display altered pH regulation by NHE1 compared with nontransformed astrocytes. Am J Physiol-Cell Physiol. 2000, 278: C676-C688.PubMedGoogle Scholar
- Xu K, Mao X, Mehta M, Cui J, Zhang C, Mao F, Xu Y: Elucidation of How Cancer Cells Avoid Acidosis through Comparative Transcriptomic Data Analysis. PloS one. 2013, 8: e71177-10.1371/journal.pone.0071177.PubMed CentralPubMedGoogle Scholar
- Harguindey S: Amiloride and its Analogs: Unique Cation Transport Inhibitors. Use of Na+/H+ Antiporter Inhibitors as a Novel Approach to Cancer Treatment. Edited by: Cragoe EJJr, ThR K, Simchowitz L. 1992, New York: VCH Publishers, 317-334.Google Scholar
- Loo SY, Chang MK, Chua CS, Kumar AP, Pervaiz S, Clement MV: NHE-1: a promising target for novel anti-cancer therapeutics. Curr Pharm Des. 2012, 18: 1372-1382. 10.2174/138161212799504885.PubMedGoogle Scholar
- Huber V, De Milito A, Harguindey S, Reshkin SJ, Wahl ML, Rauch C, Chiesi A, Pouysségur J, Gatenby RA, Rivoltini L, Fais S: Proton dynamics in cancer. J Transl Med. 2010, 8: 57-10.1186/1479-5876-8-57.PubMed CentralPubMedGoogle Scholar
- Provost JJ, Wallert MA: Inside out: targeting NHE1 as an intracellular and extracellular regulator of cancer progression. Chem Biol & Drug Design. 2013, 81: 85-101. 10.1111/cbdd.12035.Google Scholar
- Fliegel L, Fröhlich O: The Na+/H+ exchanger: an update on structure, regulation and cardiac physiology. Biochem J. 1993, 296: 273.PubMed CentralPubMedGoogle Scholar
- Jankun JS-JE: Molecular basis of specific inhibition of urokinase plasminogen activator by amiloride. Cancer Bioch Biophys. 1999, 17: 109-123.Google Scholar
- He B, Deng C, Zhang M, Zou D, Xu M: Reduction of intracellular pH inhibits the expression of VEGF in K562 cells after targeted inhibition of the Na+/H+ exchanger. Leuk Res. 2007, 31: 507-514. 10.1016/j.leukres.2006.06.015.PubMedGoogle Scholar
- Provost JJ, Rastedt D, Canine J, Ngyuen T, Haak A, Kutz C, Berthelsen N, Slusser A, Anderson K, Dorsam G: Urokinase plasminogen activator receptor induced non-small cell lung cancer invasion and metastasis requires NHE1 transporter expression and transport activity. Cell Oncol. 2012, 35: 95-110.Google Scholar
- Kim T-D, Song K-S, Li G, Choi H, Park H-D, Lim K, Hwang B-D, Yoon W-H: Activity and expression of urokinase-type plasminogen activator and matrix metalloproteinases in human colorectal cancer. BMC Cancer. 2006, 6: 211-10.1186/1471-2407-6-211. doi:210.1186/1471-2407-1186-1211PubMed CentralPubMedGoogle Scholar
- Kellen J, Mirakian A, Kolin A: Antimetastatic effect of amiloride in an animal tumour model. Anticancer Res. 1988, 8: 1373-1376.PubMedGoogle Scholar
- Harguindey S, Orive G, Pedraz J, Bello G, Arranz J, Samaniego J: Apparent cure of a cases of metastatic ovarian carcinoma alter chronic treatment with Na+-H+ antiporter inhibitors. Oncologia Madrid. 2002, 25: 472-476.Google Scholar
- Matthews H, Ranson M, Kelso M: Anti-tumour/metastasis effects of the potassium-sparing diuretic amiloride: An orally active anti-cancer drug waiting for its call-of-duty?. Intern J Cancer. 2011, 129: 2051.2061.Google Scholar
- Alliegro MC, Alliegro MA, Cragoe EJ, Glaser BM: Amiloride inhibition of angiogenesis in vitro. J Exp Zool. 1993, 267: 245-252. 10.1002/jez.1402670302.PubMedGoogle Scholar
- Junior J: Metastatic neuroendocrine carcinoma of the pancreas - case report and literature review. Rev Brasil Oncol. 2010, 7 (21): 24-30.Google Scholar
- Bellizzi A, Mangia A, Malfettone A, Cardone RA, Simone G, Reshkin SJ, Paradiso A: Na+/H+ exchanger regulatory factor 1 expression levels in blood and tissue predict breast tumour clinical behaviour. Histopathology. 2011, 58: 1086-1095. 10.1111/j.1365-2559.2011.03844.x.PubMedGoogle Scholar
- Harguindey SMF, Gonzalez Molinillo JM, Chinchilla D, Reshkin SJ, Tomoda A: Further Along a Clinical Protocol Using a Cocktail of PTIs in Human Cancer. ISPDC Abstract Book, 2nd ISPD Meeting, Nice, France, 18-19, 2011. 2011Google Scholar
- Vairo G, Cocks B, Cragoe E, Hamilton J: Selective suppression of growth factor-induced cell cycle gene expression by Na+/H+ antiport inhibitors. J Biol Chem. 1992, 267: 19043-19046.PubMedGoogle Scholar
- Hosogi SMH, Nakajima K, Ashihara E, Niisato N, Kusuzaki K, Marunaka Y: An inhibitor of Na(+)/H(+) exchanger (NHE), ethyl-isopropyl amiloride (EIPA), diminishes proliferation of MKN28 human gastric cancer cells by decreasing the cytosolic Cl(-) concentration via DIDS-sensitive pathways. Cell Physiol Biochem. 2012, 30: 1241-1253. 10.1159/000343315.PubMedGoogle Scholar
- Commisso C, Davidson SM, Soydaner-Azeloglu RG, Parker SJ, Kamphorst JJ, Hackett S, Grabocka E, Nofal M, Drebin JA, Thompson CB: Macropinocytosis of protein is an amino acid supply route in Ras-transformed cells. Nature. 2013, 497: 633-637. 10.1038/nature12138.PubMedGoogle Scholar
- Masereel B, Pochet L, Laeckmann D: An overview of inhibitors of Na+/H+ exchanger. Europ J Med Chemis. 2003, 38: 547-554. 10.1016/S0223-5234(03)00100-4.Google Scholar
- Harguindey S, Pedraz JL, Canero RG, Katin M: Edelfosine, apoptosis, MDR and Na+/H+ exchanger: induction mechanisms and treatment implications. Apoptosis. 2000, 5: 87-89. 10.1023/A:1009645927931.PubMedGoogle Scholar
- Orive G, Reshkin SJ, Harguindey S, Pedraz JL: Hydrogen ion dynamics and the Na+/H+ exchanger in cancer angiogenesis and antiangiogenesis. Br J Cancer. 2003, 89: 1395-1399. 10.1038/sj.bjc.6601286.PubMed CentralPubMedGoogle Scholar
- Mo X, Chen Q, Li X, Zheng M, Ke D, Deng W, Li G, Jiang J, Wu Z, Wang L: Suppression of NHE1 by small interfering RNA inhibits HIF-1α-induced angiogenesis in vitro via modulation of calpain activity. Microvasc Res. 2011, 81: 160-10.1016/j.mvr.2010.12.004.PubMedGoogle Scholar
- Lucien F, Brochu-Gaudreau K, Arsenault D, Harper K, Dubois CM: Hypoxia-induced invadopodia formation involves activation of NHE-1 by the p90 ribosomal S6 kinase (p90RSK). PloS one. 2011, 6: e28851-10.1371/journal.pone.0028851.PubMed CentralPubMedGoogle Scholar
- Jin W, Li Q, Wang J, Chang G, Lin Y, Li H, Wang L, Gao W, Pang T: Na+/H+ exchanger 1 inhibition contributes to K562 leukaemic cell differentiation. Cell Biol Int. 2012, 36: 739-745. 10.1042/CBI20100919.PubMedGoogle Scholar
- Busco G, Cardone RA, Greco MR, Bellizzi A, Colella M, Antelmi E, Mancini MT, Dell’Aquila ME, Casavola V, Paradiso A, Reshkin SJ: NHE1 promotes invadopodial ECM proteolysis through acidification of the peri-invadopodial space. FASEB J. 2010, 24: 3903-3915. 10.1096/fj.09-149518.PubMedGoogle Scholar
- Di Sario A, Bendia E, Omenetti A, De Minicis S, Marzioni M, Kleemann HW, Candelaresi C, Saccomanno S, Alpini G, Benedetti A: Selective inhibition of ion transport mechanisms regulating intracellular pH reduces proliferation and induces apoptosis in cholangiocarcinoma cells. Dig Liver Dis. 2007, 39: 60-69. 10.1016/j.dld.2006.07.013.PubMedGoogle Scholar
- Rupprecht H-J, Vom Dahl J, Terres W, Seyfarth KM, Richardt G, Schultheiβ H-P, Buerke M, Sheehan FH, Drexler H: Cardioprotective effects of the Na+/H+ exchange inhibitor cariporide in patients with acute anterior myocardial infarction undergoing direct PTCA. Circulation. 2000, 101: 2902-2908. 10.1161/01.CIR.101.25.2902.PubMedGoogle Scholar
- Boyce SW, Bartels C, Bolli R, Chaitman B, Chen JC, Chi E, Jessel A, Kereiakes D, Knight J, Thulin L: Impact of sodium-hydrogen exchange inhibition by cariporide on death or myocardial infarction in high-risk CABG surgery patients: results of the CABG surgery cohort of the GUARDIAN study. J Thor Cardiovasc Surg. 2003, 126: 420-427. 10.1016/S0022-5223(03)00209-5.Google Scholar
- Chaitman BR: A Review of the GUARDIAN Trial Results: Clinical Implications and the Significance of Elevated Perioperative CK‒MB on 6‒Month Survival. J Cardiac Surg. 2003, 18: 13-20. 10.1046/j.1540-8191.18.s1.3.x.Google Scholar
- Mentzer RM, Bartels C, Bolli R, Boyce S, Buckberg GD, Chaitman B, Haverich A, Knight J, Menasché P, Myers ML: Sodium-hydrogen exchange inhibition by cariporide to reduce the risk of ischemic cardiac events in patients undergoing coronary artery bypass grafting: results of the EXPEDITION study. Ann Thor Surg. 2008, 85: 1261-1270. 10.1016/j.athoracsur.2007.10.054.Google Scholar
- Zeymer U, Suryapranata H, Monassier JP, Opolski G, Davies J, Rasmanis G, Linssen G, Tebbe U, Schroder R, Tiemann R: The Na(+)/H(+) exchange inhibitor eniporide as an adjunct to early reperfusion therapy for acute myocardial infarction. Results of the evaluation of the safety and cardioprotective effects of eniporide in acute myocardial infarction (ESCAMI) trial. J Am Coll Cardiol. 2001, 38: 1644-1650. 10.1016/S0735-1097(01)01608-4.PubMedGoogle Scholar
- Theroux P, Chaitman B, Danchin N, Erhardt L, Meinertz T, Schroeder J, Tognoni G, White H, Willerson J, Jessel A: Inhibition of the sodium-hydrogen exchanger with cariporide to prevent myocardial infarction in high-risk ischemic situations: main results of the GUARDIAN trial. Circulation. 2000, 102: 3032-3038. 10.1161/01.CIR.102.25.3032.PubMedGoogle Scholar
- Avkiran M, Cook A, Cuello F: Targeting Na+/H+ exchanger regulation for cardiac protection: a RSKy approach?. Current Opin Pharmacol. 2008, 8: 133-10.1016/j.coph.2007.12.007.Google Scholar
- Linz WLHWA, Albus U: Long-term treatment with the NHE1-inhibitor cariporide extends the normal lifespan of Wistar Kyoto rats. Eur Heart J. 2001, 22: 148.Google Scholar
- Reshkin SJ, Bellizzi A, Cardone RA, Tommasino M, Casavola V, Paradiso A: Paclitaxel induces apoptosis via protein kinase A- and p38 mitogen-activated protein-dependent inhibition of the Na+/H+ exchanger (NHE) NHE isoform 1 in human breast cancer cells. Clin Cancer Res. 2003, 9: 2366-2373.PubMedGoogle Scholar
- Baartscheer A, Schumacher CA, Van Borren MM, Belterman CN, Coronel R, Opthof T, Fiolet JW: Chronic inhibition of Na+/H+-exchanger attenuates cardiac hypertrophy and prevents cellular remodeling in heart failure. Cardiovasc Res. 2005, 65: 83-92. 10.1016/j.cardiores.2004.09.024.PubMedGoogle Scholar
- Kilic A, Velic A, De Windt LJ, Fabritz L, Voss M, Mitko D, Zwiener M, Baba HA, Van Eickels M, Schlatter E: Enhanced activity of the myocardial Na+/H+ exchanger NHE-1 contributes to cardiac remodeling in atrial natriuretic peptide receptor–deficient mice. Circulation. 2005, 112: 2307-2317. 10.1161/CIRCULATIONAHA.105.542209.PubMedGoogle Scholar
- Humphreys RA, Haist JV, Chakrabarti S, Feng Q, Arnold JMO, Karmazyn M: Orally administered NHE1 inhibitor cariporide reduces acute responses to coronary occlusion and reperfusion. Amer J Physiol-Heart Circulat Physiol. 1999, 276: H749-H757.Google Scholar
- Dhein S, Salameh A: Na+/H+-Exchange Inhibition by Cariporide (Hoe 642): A New Principle in Cardiovascular Medicine. Cardiovasc Drug Revs. 1999, 17: 134-146.Google Scholar
- Brahimi-Horn MC, Chiche J, Pouysségur J: Hypoxia and cancer. J Mol Med Berl. 2007, 85: 1301-1307. 10.1007/s00109-007-0281-3.PubMedGoogle Scholar
- Brahimi-Horn C, Pouysségur J: The role of the hypoxia-inducible factor in tumor metabolism growth and invasion. Bull Cancer. 2006, 93: E73-80.PubMedGoogle Scholar
- Lv C, Yang X, Yu B, Ma Q, Liu B, Liu Y: Blocking the Na+/H+ exchanger 1 with cariporide (HOE642) reduces the hypoxia-induced invasion of human tongue squamous cell carcinoma. Intern J Oral Maxillofac Surg. 2012, 41: 1206-1210. 10.1016/j.ijom.2012.03.001.Google Scholar
- Pouysségur J, Dayan F, Mazure NM: Hypoxia signalling in cancer and approaches to enforce tumour regression. Nature. 2006, 441: 437-443. 10.1038/nature04871.PubMedGoogle Scholar
- Gao W, Chang G, Wang J, Jin W, Wang L, Lin Y, Li H, Ma L, Li Q, Pang T: Inhibition of K562 leukemia angiogenesis and growth by selective Na+/H+ exchanger inhibitor cariporide through down-regulation of pro-angiogenesis factor VEGF. Leuk Res. 2011, 35: 1506-1511. 10.1016/j.leukres.2011.07.001.PubMedGoogle Scholar
- Shi Q, Le X, Wang B, Abbruzzese JL, Xiong Q, He Y, Xie K: Regulation of vascular endothelial growth factor expression by acidosis in human cancer cells. Oncogene. 2001, 20: 3751-10.1038/sj.onc.1204500.PubMedGoogle Scholar
- Fukumura D, Xu L, Chen Y, Gohongi T, Seed B, Jain RK: Hypoxia and acidosis independently up-regulate vascular endothelial growth factor transcription in brain tumors in vivo. Cancer Res. 2001, 61: 6020-6024.PubMedGoogle Scholar
- Xu LFD, Jain RK: Acidic extracellular pH induces vascular endothelial growth factor (VEGF) in human glioblastoma cells via ERK1/2 MAPK signaling pathway: mechanism of low pH-induced VEGF. J Biol Chem. 2002, 277 (13): 11368-11374. 10.1074/jbc.M108347200.PubMedGoogle Scholar
- Yang XWD, Dong W, Song Z, Dou K: Inhibition of Na(+)/H(+) exchanger 1 by 5-(N-ethyl-N-isopropyl) amiloride reduces hypoxia-induced hepatocellular carcinoma invasion and motility. Cancer Lett. 2010, 2952: 198-204.Google Scholar
- Avery RL, Connor TB, Farazdaghi M: Systemic Amiloride Inhibits Experimentally Induced Neovascularization. Archiv Ophtalmol. 1990, 108: 1474-1476. 10.1001/archopht.1990.01070120122041.Google Scholar
- Aihara K, Hisa H, Sato T, Yoneyama F, Sasamori J, Yamaguchi F, Yoneyama S, Mizuno Y, Takahashi A, Nagai A: Cardioprotective effect of TY-12533, a novel Na(+)/H(+) exchange inhibitor, on ischemia/reperfusion injury. Europ J Pharmacol. 2000, 404: 221-229. 10.1016/S0014-2999(00)00613-0.Google Scholar
- Guzman-Perez A, Wester RT, Allen MC, Brown JA, Buchholz AR, Cook ER, Day WW, Hamanaka ES, Kennedy SP, Knight DR: Discovery of zoniporide: A potent and selective sodium–hydrogen exchanger type 1 (NHE-1) inhibitor with high aqueous solubility. Bioorg Medicin Chem Letts. 2001, 11: 803-807. 10.1016/S0960-894X(01)00059-2.Google Scholar
- Fukumoto S, Imamiya E, Kusumoto K, Fujiwara S, Watanabe T, Shiraishi M: Novel, Non-Acylguanidine-Type Na+/H+ Exchanger Inhibitors: Synthesis and Pharmacology of 5-Tetrahydroquinolinylidene Aminoguanidine Derivatives. J Med Chem. 2002, 45: 3009-3021. 10.1021/jm0104567.PubMedGoogle Scholar
- Martínez-Zaguilán R, Raghunand N, Lynch RM, Bellamy W, Martinez GM, Rojas B, Smith D, Dalton WS, Gillies RJ: pH and drug resistance. I. Functional expression of plasmalemmal V-type H+-ATPase in drug-resistant human breast carcinoma cell lines. Biochem Pharmacol. 1999, 57: 1037-1046. 10.1016/S0006-2952(99)00022-2.PubMedGoogle Scholar
- Luciani F, Spada M, De Milito A, Molinari A, Rivoltini L, Montinaro A, Marra M, Lugini L, Logozzi M, Lozupone F: Effect of proton pump inhibitor pretreatment on resistance of solid tumors to cytotoxic drugs. J Natl Ca Inst. 2004, 96: 1702-1713. 10.1093/jnci/djh305.Google Scholar
- Roepe PD, Wei LY, Cruz J, Carlson D: Lower electrical membrane potential and altered pHi homeostasis in multidrug-resistant (MDR) cells: further characterization of a series of MDR cell lines expressing different levels of P-glycoprotein. Biochemistry. 1993, 32: 11042-11056. 10.1021/bi00092a014.PubMedGoogle Scholar
- Miraglia E, Viarisio D, Riganti C, Costamagna C, Ghigo D, Bosia A: Na+/H+ exchanger activity is increased in doxorubicin-resistant human colon cancer cells and its modulation modifies the sensitivity of the cells to doxorubicin. Int J Cancer. 2005, 115: 924-929. 10.1002/ijc.20959.PubMedGoogle Scholar
- Milosavljevic N, Blanchard A, Wahl ML, Harguindey S, Poet M, Counillon L, Rauch C: Teaching new dogs old tricks: membrane biophysical properties in drug delivery and resistance. Recent Pat Anticancer Drug Discov. 2011, 6: 334-346. 10.2174/157489211796957829.PubMedGoogle Scholar
- Harguindey S, Gillis M: Evolution and cancer: possible relationships to changes in environmental hydrogen ion concentration. J Theor Biol. 1980, 86: 487-492. 10.1016/0022-5193(80)90347-1.PubMedGoogle Scholar
- Lee H-O, Silva AS, Li Y-S, Slifker M, Gatenby RA, Cheng JD: Evolution of tumor invasiveness: the adaptive tumor microenvironment landscape model. Cancer Res. 2011, 71: 6327-6337. 10.1158/0008-5472.CAN-11-0304.PubMed CentralPubMedGoogle Scholar
- Alfarouk KO, Ibrahim ME, Gatenby RA, Brown JS: Riparian ecosystems in human cancers. Evolut Applications. 2013, 6: 46-53. 10.1111/eva.12015.Google Scholar
- De Milito A, Fais S: Tumor acidity, chemoresistance and proton pump inhibitors. Future Oncol. 2005, 1: 779-786. 10.2217/14796618.104.22.1689.PubMedGoogle Scholar
- Li J, Eastman A: Apoptosis in an Interleukin-2-dependent Cytotoxic T Lymphocyte Cell Line Is Associated with Intracellular Acidification. Role of the Na+/H+ antiport. J Biol Chem. 1995, 270: 3203-3211. 10.1074/jbc.270.7.3203.PubMedGoogle Scholar
- Pérez-Sala D, Collado-Escobar D, Mollinedo F: Intracellular alkalinization suppresses lovastatin-induced apoptosis in HL-60 cells through the inactivation of a pH-dependent endonuclease. J Biol Chem. 1995, 270: 6235-6242. 10.1074/jbc.270.11.6235.PubMedGoogle Scholar
- Reynolds JE, Li J, Craig RW, Eastman A: BCL-2 and MCL-1 expression in Chinese hamster ovary cells inhibits intracellular acidification and apoptosis induced by staurosporine. Exp Cell Res. 1996, 225: 430-436. 10.1006/excr.1996.0194.PubMedGoogle Scholar
- Keizer HG, Joenje H: Increased cytosolic pH in multidrug-resistant human lung tumor cells: effect of verapamil. J Nat Cancer Inst. 1989, 81: 706-709. 10.1093/jnci/81.9.706.PubMedGoogle Scholar
- Lagadic-Gossmann D, Huc L, Lecureur V: Alterations of intracellular pH homeostasis in apoptosis: origins and roles. Cell Death Differ. 2004, 11: 953-961. 10.1038/sj.cdd.4401466.PubMedGoogle Scholar
- De Milito AFS: Proton pump inhibitors may reduce tumour resistance. Expert Opin Pharmacother. 2005, 6: 1049-1054. 10.1517/14656522.214.171.1249.PubMedGoogle Scholar
- Fais S: Proton pump inhibitor‒induced tumour cell death by inhibition of a detoxification mechanism. J Int Med. 2010, 267: 515-525. 10.1111/j.1365-2796.2010.02225.x.Google Scholar
- Lindner D, Raghavan D: Intra-tumoural extra-cellular pH: a useful parameter of response to chemotherapy in syngeneic tumour lines. Br J Cancer. 2009, 100: 1287-1291. 10.1038/sj.bjc.6605022.PubMed CentralPubMedGoogle Scholar
- Torigoe T, Izumi H, Ise T, Murakami T, Uramoto H, Ishiguchi H, Yoshida Y, Tanabe M, Nomoto M, Kohno K: Vacuolar H+-ATPase: functional mechanisms and potential as a target for cancer chemotherapy. Anticancer Drugs. 2002, 13: 237-243. 10.1097/00001813-200203000-00005.PubMedGoogle Scholar
- Murakami T, Shibuya I, Ise T, Chen ZS, Akiyama S, Nakagawa M, Izumi H, Nakamura T, Matsuo K, Yamada Y: Elevated expression of vacuolar proton pump genes and cellular pH in cisplatin resistance. Intern J Cancer. 2001, 93: 869-874. 10.1002/ijc.1418.Google Scholar
- Paris S, Pouysségur J: Growth factors activate the Na+/H+ antiporter in quiescent fibroblasts by increasing its affinity for intracellular H+. J Biol Chem. 1984, 259: 10989-10994.PubMedGoogle Scholar
- Thiebaut F, Currier S, Whitaker J, Haugland R, Gottesman M, Pastan I, Willingham M: Activity of the multidrug transporter results in alkalinization of the cytosol: measurement of cytosolic pH by microinjection of a pH-sensitive dye. J Histochem Cytochemist. 1990, 38: 685-10.1177/38.5.1692055.Google Scholar
- Boscoboinik D, Gupta R, Epand R: Investigation of the relationship between altered intracellular pH and multidrug resistance in mammalian cells. Br J Cancer. 1990, 61: 568-10.1038/bjc.1990.127.PubMed CentralPubMedGoogle Scholar
- Rauch C, Pluen A: Multi drug resistance-dependent “vacuum cleaner” functionality potentially driven by the interactions between endocytosis, drug size and Pgp-like transporters surface density. Europ Biophs J. 2007, 36: 121-131. 10.1007/s00249-006-0113-3.Google Scholar
- Thews O, Gassnery B, Kelleher DK, Schwerdty G, Gekley M: Impact of Extracellular Acidity on the Activity of P-glycoprotein and the Cytotoxicity of Chemotherapeutic Drugs. Neoplasia. 2006, 8: 143-152. 10.1593/neo.05697.PubMed CentralPubMedGoogle Scholar
- Rauch C, BA W, Eleanor D, Miriam L, Wahl , Harguindey S: Cell Membranes, Cytosolic pH and Drug Transport in Cancer and MDR: Physics, Biochemistry and Molecular Biology. Multiple Drug Resistance. Edited by: Agoston M, Gusztav B. 2009, Hauppauge NY: Nova Science Publishers, Inc, 1-24.Google Scholar
- Weichert A, Faber S, Jansen H, Scholz W, Lang H: Synthesis of the highly selective Na+/H+ exchange inhibitors cariporide mesilate and (3-methanesulfonyl-4-piperidino-benzoyl) guanidine methanesulfonate. Arzneimittelforschung. 1997, 47: 1204.PubMedGoogle Scholar
- Parks SK, Mazure NM, Counillon L, Pouysségur J: Hypoxia promotes tumor cell survival in acidic conditions by preserving ATP levels. J Cell Physiol. 2013, 28 (9): 1854-1862.Google Scholar
- L’Allemain G, Franchi A, Cragoe E, Pouysségur J: Blockade of the Na+/H+ antiport abolishes growth factor-induced DNA synthesis in fibroblasts. Structure-activity relationships in the amiloride series. J Biol Chem. 1984, 259: 4313-4319.PubMedGoogle Scholar
- Fang B, Wang D, Huang M, Yu G, Li H: Hypothesis on the Relationship Between the Change in Intracellular pH and Incidence of Sporadic Alzheimer’s Disease or Vascular Dementia. Internat J Neurosci. 2010, 120: 591-595. 10.3109/00207454.2010.505353.Google Scholar
- Vincent AM, TenBroeke M, Maiese K: Neuronal intracellular pH directly mediates nitric oxide‒induced programmed cell death. J Neurobiol. 1999, 40: 171-184. 10.1002/(SICI)1097-4695(199908)40:2<171::AID-NEU4>3.0.CO;2-F.PubMedGoogle Scholar
- Rauch C: Toward a mechanical control of drug delivery. On the relationship between Lipinski’s 2nd rule and cytosolic pH changes in doxorubicin resistance levels in cancer cells: a comparison to published data. Eur Biophys J. 2009, 38: 829-846. 10.1007/s00249-009-0429-x.PubMedGoogle Scholar
- Raghunand N, He X, Van Sluis R, Mahoney B, Baggett B, Taylor C, Paine-Murrieta G, Roe D, Bhujwalla Z, Gillies R: Enhancement of chemotherapy by manipulation of tumour pH. Brit J Cancer. 1999, 80: 1005-10.1038/sj.bjc.6690455.PubMed CentralPubMedGoogle Scholar
- Iessi E, Marino ML, Lozupone F, Fais S, De Milito A: Tumor acidity and malignancy: novel aspects in the design of anti-tumor therapy. Cancer Ther. 2008, 6: 55-66.Google Scholar
- Altan N, Chen Y, Schindler M, Simon SM: Defective acidification in human breast tumor cells and implications for chemotherapy. J Exp Med. 1998, 187: 1583-1598. 10.1084/jem.187.10.1583.PubMed CentralPubMedGoogle Scholar
- Larsen AK, Escargueil AE, Skladanowski A: Resistance mechanisms associated with altered intracellular distribution of anticancer agents. Pharmacol Therap. 2000, 85: 217-229. 10.1016/S0163-7258(99)00073-X.Google Scholar
- Raghunand N, Mahoney BP, Gillies RJ: Tumor acidity, ion trapping and chemotherapeutics: II. pH-dependent partition coefficients predict importance of ion trapping on pharmacokinetics of weakly basic chemotherapeutic agents. Biochem Pharmacol. 2003, 66: 1219-1229. 10.1016/S0006-2952(03)00468-4.PubMedGoogle Scholar
- Raghunand N, Martı́nez–Zaguilán R, Wright SH, Gillies RJ: pH and drug resistance. II. Turnover of acidic vesicles and resistance to weakly basic chemotherapeutic drugs. Biochem Pharmacol. 1999, 57: 1047-1058. 10.1016/S0006-2952(99)00021-0.PubMedGoogle Scholar
- Rauch C: On the relationship between drug’s size, cell membrane mechanical properties and high levels of multi drug resistance: a comparison to published data. Europ Biophys J. 2009, 38: 537-546. 10.1007/s00249-008-0385-x.Google Scholar
- Bell C, Hill C, Burton C, Blanchard A, Shephard F, Rauch C: Importance of the Difference in Surface Pressures of the Cell Membrane in Doxorubicin Resistant Cells That do not Express Pgp and ABCG2. Cell Biochem Biophys. 2013, 1: 14.Google Scholar
- De Milito A, Iessi E, Logozzi M, Lozupone F, Spada M, Marino ML, Federici C, Perdicchio M, Matarrese P, Lugini L: Proton pump inhibitors induce apoptosis of human B-cell tumors through a caspase-independent mechanism involving reactive oxygen species. Ca Res. 2007, 67: 5408-5417. 10.1158/0008-5472.CAN-06-4095.Google Scholar
- De Milito A, Canese R, Marino ML, Borghi M, Iero M, Villa A, Venturi G, Lozupone F, Iessi E, Logozzi M: pH‒dependent antitumor activity of proton pump inhibitors against human melanoma is mediated by inhibition of tumor acidity. Internat J Cancer. 2010, 127: 207-219. 10.1002/ijc.25009.Google Scholar
- Ruiz-Meana M, Garcia-Dorado D, Pina P, Inserte J, Agulló L, Soler-Soler J: Cariporide preserves mitochondrial proton gradient and delays ATP depletion in cardiomyocytes during ischemic conditions. Am J Physiol-Heart Circulat Physiol. 2003, 285: H999-H1006.Google Scholar
- Marches R, Vitetta ES, Uhr JW: A role for intracellular pH in membrane IgM-mediated cell death of human B lymphomas. PNAS U S A. 2001, 98: 3434-3439. 10.1073/pnas.061028998.Google Scholar
- Severin T, Müller B, Giese G, Uhl B, Wolf B, Hauschildt S, Kreutz W: pH-dependent LAK cell cytotoxicity. Tumor Biol. 2009, 15: 304-310.Google Scholar
- Lardner A: The effects of extracellular pH on immune function. J Leuk Biol. 2001, 69: 522-530.Google Scholar
- Loeffler D, Juneau P, Heppner G: Natural killer-cell activity under conditions reflective of tumor micro-environment. Intern J Cancer. 1991, 48: 895-10.1002/ijc.2910480617.Google Scholar
- Fischer B, Müller B, Fischer K-G, Baur N, Kreutz W: Acidic pH inhibits non-MHC-restricted killer cell functions. Clinic Immunol. 2000, 96: 252-263. 10.1006/clim.2000.4904.Google Scholar
- Fischer B, Müller B, Fisch P, Kreutz W: An acidic microenvironment inhibits antitumoral non-major histocompatibility complex-restricted cytotoxicity: implications for cancer immunotherapy. J Immunother. 2000, 23: 196-207. 10.1097/00002371-200003000-00004.PubMedGoogle Scholar
- Haveman J: The pH of the cytoplasm as an important factor in the survival of in vitro cultured malignant cells after hyperthermia. Effects of carbonylcyanide 3-chlorophenylhydrazone. Eur J Cancer. 1979, 15: 1281-1288. 10.1016/0014-2964(79)90255-X.PubMedGoogle Scholar
- Haveman J: The influence of pH on the survival after X-irradiation of cultured malignant cells. Effects of carbonylcyanide-3-chlorophenylhydrazone. Int J Rad Biol. 1980, 37 (2): 201-205. 10.1080/09553008014550241.Google Scholar
- Choi SYCC, Gout PW, Wang Y: Cancer-generated lactic acid: a regulatory, immunosuppressive metabolite?. J Pathol. 2013, 230 (4): 350-355. 10.1002/path.4218.PubMed CentralPubMedGoogle Scholar
- Shi Y, Kim D, Caldwell M, Sun D: The role of Na(+)/h(+) exchanger isoform 1 in inflammatory responses: maintaining H(+) homeostasis of immune cells. Adv Exp Med Biol. 2013, 961: 411-418. 10.1007/978-1-4614-4756-6_35.PubMedGoogle Scholar
- Arig I-H, Wojtkowiak JW, Cohelo Ribeiro ML, Estrella V, Bailey KM, Cornnell HH, Gatenby RA, Gillies RJ: Free Base Lysine Increases Survival and Reduces Metastasis in Prostate Cancer Model. J Cancer Sci Ther. 2011, Suppl 1 (4): 1-7.http://dx.doi.org/10.4172/1948-5956.S1-004,Google Scholar
- Robey IF, Baggett BK, Kirkpatrick ND, Roe DJ, Dosescu J, Sloane BF, Hashim AI, Morse DL, Raghunand N, Gatenby RA, Gillies RJ: Bicarbonate increases tumor pH and inhibits spontaneous metastases. Cancer Res. 2009, 69: 2260-2268. 10.1158/0008-5472.CAN-07-5575.PubMed CentralPubMedGoogle Scholar
- Spugnini EP, Baldi A, Buglioni S, Carocci F, De Bazzichini GM, Betti G, Pantaleo I, Menicagli F, Citro G, Fais S: Lansoprazole as a rescue agent in chemoresistant tumors: a phase I/II study in companion animals with spontaneously occurring tumors. J Transl Med. 2011, 9: 221-10.1186/1479-5876-9-221.PubMed CentralPubMedGoogle Scholar
- Robey IF, Martin NK: Bicarbonate and dichloroacetate: evaluating pH altering therapies in a mouse model for metastatic breast cancer. BMC Cancer. 2011, 11: 235-10.1186/1471-2407-11-235.PubMed CentralPubMedGoogle Scholar
- Sparks R, Pool T, Smith N, Cameron I: Effects of amiloride on tumor growth and intracellular element content of tumor cells in vivo. Ca Res. 1983, 43: 73-77.Google Scholar
- Cragoe EJ, Kleyman TR, Simchowitz L: Amiloride and its Analogs: Unique Cation Transport Inhibitors. 1992, New York: Wiley-VCH PublishersGoogle Scholar
- Lorrain J, Briand V, Favennec E, Duval N, Grosset A, Janiak P, Hoornaert C, Cremer G, Latham C, O’Connor SE: Pharmacological profile of SL 59.1227, a novel inhibitor of the sodium/hydrogen exchanger. British J Pharmacol. 2000, 131: 1188-1194. 10.1038/sj.bjp.0703671.Google Scholar
- Atwal KS, O’Neil SV, Ahmad S, Doweyko L, Kirby M, Dorso CR, Chandrasena G, Chen BC, Zhao R, Zahler R: Synthesis and biological activity of 5-aryl-4-(4-(5-methyl-1H-imidazol-4-yl)piperidin-1-yl)pyrimidine analogs as potent, highly selective, and orally bioavailable NHE-1 inhibitors. Bioorg Med Chem Lett. 2006, 16: 4796-4799. 10.1016/j.bmcl.2006.06.077.PubMedGoogle Scholar
- Harguindey S: Ph D Thesis. The pH in the Etiopathogenesis and Treatment of Cancer. 1990, Bilbao, Spain: Department of Embriology, The University of the Basque Country (EHU)Google Scholar
- Gatenby RA: A change of strategy in the war on cancer. Nature. 2009, 459: 508-509. 10.1038/459508a.PubMedGoogle Scholar
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