Lenalidomide normalizes tumor vessels in colorectal cancer improving chemotherapy activity
- V. Leuci1, 2,
- F. Maione4,
- R. Rotolo1, 2,
- E. Giraudo4, 8,
- F. Sassi5,
- G. Migliardi5,
- M. Todorovic2,
- L. Gammaitoni2,
- G. Mesiano2,
- L. Giraudo2,
- P. Luraghi7,
- F. Leone1, 3,
- F. Bussolino1, 6,
- G. Grignani3,
- M. Aglietta1, 3,
- L. Trusolino1, 5,
- A. Bertotti†1, 5 and
- D. Sangiolo†1, 2Email author
© Leuci et al. 2016
Received: 9 July 2015
Accepted: 20 April 2016
Published: 5 May 2016
Angiogenesis inhibition is a promising approach for treating metastatic colorectal cancer (mCRC). Recent evidences support the seemingly counterintuitive ability of certain antiangiogenic drugs to promote normalization of residual tumor vessels with important clinical implications. Lenalidomide is an oral drug with immune-modulatory and anti-angiogenic activity against selected hematologic malignancies but as yet little is known regarding its effectiveness for solid tumors. The aim of this study was to determine whether lenalidomide can normalize colorectal cancer neo-vessels in vivo, thus reducing tumor hypoxia and improving the benefit of chemotherapy.
We set up a tumorgraft model with NOD/SCID mice implanted with a patient-derived colorectal cancer liver metastasis. The mice were treated with oral lenalidomide (50 mg/Kg/day for 28 days), intraperitoneal 5-fluorouracil (5FU) (20 mg/Kg twice weekly for 3 weeks), combination (combo) of lenalidomide and 5FU or irrelevant vehicle. We assessed tumor vessel density (CD146), pericyte coverage (NG2; alphaSMA), in vivo perfusion capability of residual vessels (lectin distribution essay), hypoxic areas (HP2-100 Hypoxyprobe) and antitumor activity in vivo and in vitro.
Treatment with lenalidomide reduced tumor vessel density (p = 0.0001) and enhanced mature pericyte coverage of residual vessels (p = 0.002). Perfusion capability of tumor vessels was enhanced in mice treated with lenalidomide compared to controls (p = 0.004). Accordingly, lenalidomide reduced hypoxic tumor areas (p = 0.002) and enhanced the antitumor activity of 5FU in vivo. The combo treatment delayed tumor growth (p = 0.01) and significantly reduced the Ki67 index (p = 0.0002). Lenalidomide alone did not demonstrate antitumor activity compared to untreated controls in vivo or against 4 different mCRC cell lines in vitro.
We provide the first evidence of tumor vessel normalization and hypoxia reduction induced by lenalidomide in mCRC in vivo. This effect, seemingly counterintuitive for an antiangiogenic compound, translates into indirect antitumor activity thus enhancing the therapeutic index of chemotherapy. Our findings suggest that further research should be carried out on synergism between lenalidomide and conventional therapies for treating solid tumors that might benefit from tumor vasculature normalization.
KeywordsLenalidomide Colorectal cancer Tumor-vessel normalization
Angiogenesis inhibition has shown promising therapeutic activity against metastatic colorectal cancer (mCRC). VEGF blockade by the monoclonal antibody bevacizumab is currently incorporated in clinical practice and other compounds with similar activity are being explored in clinical trials [1–8]. These approaches are based on the idea of starving tumors thus preventing or reducing neovasculature formation [9–11]. Recent evidences have demonstrated that another promising, and seemingly counterintuitive, aspect of some antiangiogenic compounds is the potential to promote the normalization of tumor vessels [12–15], which are typically immature and disorganized in tumors [10, 16]. This effect may have therapeutic benefit by enhancing tumor oxygenation, delivery of therapeutic compounds or even immune effector cells [17–19]. Abnormal tumor vasculature reduces blood flow into tumor sites, potentially hindering the delivery of chemotherapy drugs and thus promoting an aggressive hypoxic microenvironment that fuels a vicious circle which results in the upregulation of pro-angiogenic factors [20–23]. Improved chemotherapy outcome was associated with vessel normalization in preclinical tumor models [24–27]. Assessment of vessel normalization is often based on morphologic vessel remodeling with functional evidences of mature pericyte-coverage and restored perfusion ability with consequent variation in tissue oxygenation/hypoxia status [28–30]. Awareness of the importance of tumor-vessel normalization could modify and enrich the old idea of anti-angiogenic therapy. Further research is required to explore the effect of antiangiogenic compounds on vessel-normalization in settings such as mCRC, where antiangiogenesis is considered to be a significant clinical approach. Lenalidomide is an oral derivative of thalidomide, currently approved for treating selected hematologic malignancies such as multiple myeloma and 5q- myelodysplastic syndrome [31–35]. Although the antitumor mechanism of lenalidomide is not yet completely clear, it seems to induce angiogenesis inhibition and immunomodulation [36, 37]. Initial experimental trials are exploring the activity of lenalidomide in mCRC. These studies are aimed at exploiting the immunomodulation property of lenalidomide in order to increase the activity of anti-EGFR mAb cetuximab [38, 39].
We hypothesized that lenalidomide might exert an additional beneficial effect on antiangiogenic and tumor-vessel normalization activity.
Indeed although it is assumed, tumor-vessel normalization has not yet been effectively explored. We set a preclinical mCRC model based on a single patient-derived tumorgraft model generated from a sample of liver CRC metastasis [40, 41]. This model was shown to be representative of the original patient’s tumor. It helps to retain the actual tumor tissue architecture, thus providing a platform for studying issues such as tumor neo-vessels and their modulation in vivo. This model was used to explore the antiangiogenic and normalization effects of oral lenalidomide on CRC neo-vessels, including its potential to improve tumor perfusion, oxygenation and the therapeutic index of conventional chemotherapy.
Tumor cell lines
All colorectal cancer cell lines were obtained by means of American type culture collection (ATCC). Appropriate culture medium [HCT116 and LS513 grown in RPMI-1640 medium, SKCO-1 grown in DMEM medium, and LoVo grown in F-12 K medium; American type culture collection (ATCC)] was supplemented with 10 % FBS (Sigma), 100 U/mL penicillin and 100 U/mL streptomycin (Sigma) in a humidified 5 % CO2 incubator at 37 °C.
Murine CRC patient-derived tumorgraft
All animal procedures were approved by the internal animal research ethical committee and the Italian Ministry of Health. The metastatic CRC sample was obtained by carrying out a liver metastasectomy on a patient treated at our center. Before the surgical intervention the patient was treated with four courses of neo-adjuvant chemotherapy with capecitabine and oxaliplatin. The tumor presented the following genetic mutations: KRAS (p.G12C), APC (p.K1370*) and TP53 (p.V173E). The patient provided informed consent and the study was conducted according to a protocol approved by the institutional review board. Tumor material not required for histopathologic analysis was collected and placed in medium 199 supplemented with 200 U/mL penicillin, 200 μg/mL streptomycin, and 100 μg/mL levofloxacin. Each sample was cut into 25- to 30 mm3 pieces in antibiotic-containing medium; some of the pieces were incubated overnight in RNA later and then frozen at −80 °C for molecular analyses; 2 other pieces were coated in Matrigel (BD Biosciences) and implanted in 2 different 4- to 6-week-old female NOD (nonobese diabetic)/SCID (severe combined immunodeficient) mice (Charles River). After mass formation, the tumors were passaged and expanded for 2 generations until production of a cohort of 32 mice [41, 42]. Four-week-old NOD/SCID mice with established tumors (average volume 400 mm3) were divided into four groups (8 mice per group) and treated with oral lenalidomide (kindly provided by Celgene) 50 mg/Kg/day for 28 days, intraperitoneal 5-Fluorouracile (5FU) (20 mg/Kg twice weekly for 3 weeks) from pharmacy leftovers, combination of lenalidomide and 5FU (doses as previously indicated) or irrelevant vehicle (0.5 % carboxymethylcellulose and 0.25 % polyoxyethylene sorbitan monooleate (Tween® 80) in sterile water) respectively. Lenalidomide was administered to the mice via oral gavage at the above indicated dose in an aqueous suspension containing 0.5 % carboxymethylcellulose and 0.25 % Tween® 80 at a dose volume of 5 mL/kg.
Tumor size was evaluated weekly by taking caliper measurements and the approximate volume of the mass was calculated with the formula 4/3 × π(d/2)2 × D/2, where d is the minor tumor axis and D is the major tumor axis. The tumor was fixed overnight in 4 % paraformaldehyde, dehydrated, paraffin-embedded, sectioned (5 μm) and stained with hematoxylin and eosin (H&E.; Bio Optica).
The percentage of tumor growth inhibition for each arm of treatment was calculated with the Eq. 100 − (T/C × 100), where T is the mean relative tumor volume (RTV) of the treated tumor and C is the mean RTV in the control group at the time of sacrifice.
The individual RTV was defined as Vx/V1, where Vx is the volume in mm3 at the end of the experiment and V1 at the start of treatment.
Paraffin-embedded or OCT-embedded frozen samples were cut into 5-μm thick sections. The tissue slides were treated according to standard immunofluorescence or immunohistochemistry procedures. In short, the slides were permeabilized in 0.1 % Triton X-100 and 0.3 % Tween 20 (Sigma-Aldrich) in TBS, treated for 30 min with 1 % hydrogen peroxide to quench endogenous peroxidases in immunohistochemistry experiments, and saturated with 5 % goat serum (Sigma-Aldrich) in PBS. The slides were incubated with individual primary antibodies overnight at 4 °C inside a moist chamber. After rinsing in PBS, a secondary antibody was added. Secondary HRP-conjugate antibodies (EnVision; DakoCytomation) were used for immunohistochemistry and the reaction was visualized with DAB chromogen (DakoCytomation Liquid DAB Substrate Chromogen System, Dako). The tissues were counterstained with Mayer hematoxylin (Bio-Optica), mounted on glass slides and visualized with a BX-60 microscope (Olympus) equipped with a color Qicam Fast 1394-digital CCD camera (12 bit; QImaging). For carrying out the immunofluorescence experiments, Alexa Fluor secondary antibodies were used conjugated with Alexa Fluor 488 or Alexa Fluor 555 fluorochromes (Invitrogen). Molecular probes were used for counterstaining the nuclei with DAPI (Invitrogen). The slides were analyzed under a Leica DM IRBM microscope. The tissues were stained with the following primary antibodies: anti–Ki-67 (DAKO); Anti-MCAM [CD146] (clone EPR3208, Millipore); purified rat monoclonal anti-panendothelial cell ANTIGEN (Meca32) (550563, clone Meca32, 1:100, BD Pharmingen); rabbit polyclonal anti-α-SMA (AB5694, 1:100, Abcam).
Tumor vasculature quantification
Tumor vasculature was evaluated by immunohistochemistry. For each animal, the total vessel area in each tumor section was quantified as CD146 positive structures by computer assisted analysis employing Image-ProPlus 6.2 software (Media Cybernetics). The CD146 positive surface area occupied by vessels was compared with total tissue area. In order to better account for the elevated intratumoral heterogeneity, at least 25 microscopic observational fields (MOF) (40× magnification) were recorded and analyzed from sections of 5 tumors for each experimental condition (40× magnification).
Immunofluorescence analysis for pericyte coverage and tumor vessel perfusion
All immunofluorescence images were captured and analyzed with a Leica SPIIE confocal laser-scanning microscope (Leica Microsystems). Image acquisition was performed maintaining the same laser power, gain, and offset settings in order to quantify pericyte coverage (α-SMA and NG2 markers shown by red and green channels, respectively) and at least 16 multiple observational fields (40× magnification) from sections of 3 tumors for each experimental condition were recorded and analyzed. We drew a region of interest (ROI) close to each blood vessel (Meca32, shown by violet channels) and then quantified the MFI of red/green and violet channels using the LAS AF Quantification Tool. We then calculated the ratio between red/green and violet channels for each ROI. In this way the pericyte values were normalized on the vessel area. A similar procedure was used for quantifying vascular perfusion by FITC-labeled lectin (Vector laboratories, Inc.) shown by the green channel. The mice were injected i.v. with 0.05 mg FITC-labeled tomato lectin (Lycopersicon esculentum; Vector Laboratories) and were euthanized after 2 min. The lectin distribution was visualized by means of fluorescent confocal microscopy. The experiments included at least 16 MOF (40× magnification) from sections of 3 tumors for each experimental condition.
Tumor hypoxia analysis
The amount of tumor hypoxia was determined 15 min after injecting 60 mg/kg pimonidazole hydrochloride (HP2-100 Hypoxyprobe Kit-Plus; Natural Pharmacia International Inc.) into NOD/SCID mice . The formation of pimonidazole adducts was detected by immunostaining with Hypoxyprobe-1-Mab1 FITC Ab according to the manufacturer’s instructions. Immunofluorescence images were captured and analyzed with a Leica SPIIE confocal laser-scanning microscope (Leica Microsystems).
Immunostaining with Hypoxyprobe-1-Mab1 FITC Ab was quantified in at least 10 multiple observational fields (40× magnification) from sections of three tumors for each experimental condition. In order to quantify hypoxic areas in each image, we drew a Region of Interest (ROI) close to each green area (pimonidazole adducts, shown by green channel) and a ROI close to each viable tissue area (DAPI, shown by blue channels) and we then quantified the area with Image-ProPlus 6.2 software (Media Cybernetics). The ratio between the green and blue areas was calculated and the values were expressed as percentages.
Cell viability assays
Four CRC cell lines (HCT116, LS513, SKCO-1 and LoVo cells) were plated at a density of 10 cells/μL in complete growth medium and seeded in 96-well plastic culture plates (Day 0). On Day 1, 100 μl of lenalidomide (Celgene) (10 μM), 5 FU (10 μM), combination of lenalidomide and 5FU or irrelevant vehicle were added to the cells. On Day 3, cell viability was assessed by quantifying the ATP content by means of a luminescence assay (CellTiter-Glo, Promega). All measurements were recorded with a GloMax 96 Microplate Luminometer (Promega). Growth inhibition at each drug concentration was normalized to vehicle-treated cells.
The means and standard errors were calculated as appropriate. Three or more groups (tumor samples from mice treated with lenalidomide, 5-FU, Combo and irrelevant vehicle) were compared with one-way ANOVA and post analysis comparisons were carried out among each group with Bonferroni post-test analysis. Curves representing tumor growth in mice treated with lenalidomide, 5-FU, Combo and vehicle-treated controls were compared with two-way ANOVA and post analysis comparisons among each group were carried out with Bonferroni post-test analysis. Combo and vehicle treated controls were compared with unpaired t test. Values < 0.05 were considered statistically significant. The results were analyzed with GraphPad Prism5 software, where the P value has the following meaning: (*) P ≤ 0.05; (**) P ≤ 0.01; (***) P ≤ 0.001; (****) P ≤ 0.0001.
Tumor vessel density and pericyte coverage in residual tumor vessels
Vessel perfusion capability and effect on tumor hypoxia
Vessel normalization enhances chemotherapy activity
Statistical significance (t test) of combination treatment versus vehicle was reached relatively to CD146 expression (22 ± 3 %, p < 0.0001), perfusion capability (MFI lectin/MECA32 = 0.4 ± 0.1; p < 0.0001) and hypoxia (hypoxic area 1 ± 0.5 %; p < 0.001).
Lenalidomide is devoid of direct tumoricidal activity
We reported the first evidence that lenalidomide induces normalization of tumor neo-vasculature with improved tissue oxygenation and potential therapeutic benefit in a preclinical in vivo tumorgraft model of mCRC. Lenalidomide is currently used for treating selected hematologic malignancies but as yet little is known regarding its effectiveness for solid tumors. Our findings were obtained in a preclinical tumor xenograft model generated with a liver metastasis from a mCRC patient. Even if potentially limited by its single-patient origin, tumorgrafts may favorable compare with cell line based models for analyzing issues such as maturation and functionality of tumor vessels. Possible strengths are related to the preservation of tumor-architecture, even acknowledging that tumor neo-vessels are mainly murine, and limitation of genetic drift .
Lenalidomide has recently been explored in the setting of mCRC with the aim of exploiting its immunomodulation activity for potentiating the ADCC effect induced by cetuximab. Our findings suggest the added value of lenalidomide and broaden its potentialities. In particular our data may further support synergisms with immunotherapy approaches, as the functionality of the vessel network is essential for improving the tumor homing of immune effectors. The conventional angiogenesis inhibition that is expected when treating with lenalidomide was confirmed in our model and the hypothesized “normalization” effect was evident on residual vessels within tumors.
We observed that tumor xenografts treated with lenalidomide in association with 5-FU presented a clear trend towards the (re)differentiation of single cells and global tissue architecture, resembling features of normal colon epithelium, indirectly supporting the beneficial activity of chemotherapy. Several morphologic or molecular parameters may be considered to be indicative of vessel normalization, but ultimately this phenomenon remains a “functional concept” supported by the ability to restore physiologic blood flow and tissue oxygenation. We showed that lenalidomide significantly increased in vivo perfusion capability of residual tumor vessels with regular structures and mature pericyte coverage.
The aim of this study was not to confirm mechanistic molecular mechanisms underlying the activity of lenalidomide as it has already been investigated in previous studies. Based on preclinical evidence, lenalidomide may inhibit VEGF [44, 45], hinder b-FGF-induced endothelial cell cord formation in hypoxic conditions and/or block VEGF-induced endothelial cell Akt phosphorylation, HIF-1α expression and association of the adherent junction proteins in endothelial cells . Instead we focused on the functional implications of this effect. The improvement in tissue oxygenation observed is indicative of normalized blood flow, which may occur to break the vicious circle between the hypoxia-induced factors that promote dysfunctional angiogenesis.
A restored vasculature is important for the efficacy of therapeutic interventions and enhanced activity of chemotherapy with 5-FU was observed. A limitation of our model is its derivation from a single patient’s tumors and may not be representative of all CRCs. Of course, it was not our aim to propose a new therapeutic combination or to demonstrate the known activity of 5-FU against mCRC. The activity of 5-FU was explored only as an experimental tool to confirm the possible functional implications of lenalidomide-induced vessel normalization. Our results provide proof of concept that chemotherapy may indirectly benefit from the activity of lenalidomide on tumor vasculature and the same principle could be applied to other active drugs in mCRC. Moreover, our findings may provide a favorable biological platform for immunotherapy interventions . Functional and restored vessel network is essential for the activity of either approved anti EGFR mAb  or other experimental strategies such as novel immune-checkpoint modulators and adoptive cell therapies [26, 49–52]. Ultimately all these strategies rely on the effective trafficking and homing of immune effectors at tumor sites that could consequently benefit from the healthy status of tumor vessels. Furthermore, lenalidomide is endowed with intrinsic immunomodulatory activity, promoting activation of NK and Cytotoxic T cells, potentially fueling a positive biological loop.
Our findings provide proof of concept that lenalidomide may have indirect, clinically relevant activity in the challenging setting of mCRC. The observed vessel-normalization effect is consistent with the concept of antiangiogenesis as part of a composite therapeutic strategy that benefits from reduced yet functional tumor vasculature. Our data may be useful for carrying out future experimental clinical trials incorporating lenalidomide in order to improve the efficacy of treatments against mCRC. Further preclinical studies are required to in order to determine whether the observed activity of lenalidomide may be extended to other forms of solid tumors and be used in combination with other immunotherapy strategies.
metastatic colorectal cancer
region of interest
neural antigen 2
alpha smooth muscle actin
vascular endothelial growth factor
basic fibroblast growth factor
hypoxia-inducible factor 1-alpha
epidermal growth factor receptor
nonobese diabetic/severe combined immunodeficiency
antibody-dependent cell-mediated cytotoxicity
mean fluorescence intensity
mycroscopic observational field
VL designed and performed the experiments, analyzed the data and contributed to the preparation of the manuscript; FM and EG carried out in vivo experiments on tumor vessel perfusion and tumor hypoxia, furthermore participated in critical revision of the manuscript; RR and GM performed immunohistochemistry, immunofluorescence and contributed to manuscript writing and revision; FS was involved in all the histological examinations and tumor proliferation essays; LG, GM set up the tumorgraft model and carried out animal treatment with drugs; MT, PL performed and analyzed in vitro experiments; LT, FB contributed to the in vivo experimental design and critical revision of the manuscript; MA, FL, GG were involved in clinical management of the patient, collection and processing of biologic material; AB and DS conceived, supervised the study, and drafted the manuscript. All authors read and approved the final manuscript.
This study was financed in part by the “Associazione Italiana Ricerca sul Cancro” (AIRC) MFAG 2014 N.15731; IG. Grant. N.11515, FPRC ONLUS 5 × 1000, Ministero della Salute 2012; Ricerca Finalizzata-Giovani Ricercatori Ministero della Salute (GR-2011-02349197), University of Torino Fondo Ricerca Locale 2013; the AIRC Italian Association for Cancer Research (Special Program Molecular Clinical Oncology 5 × 1000, project 9970 to MA and LT), AIRC IGs (Investigator Grants) project 14205 (to LT) and project 15571 (to AB); MIUR 2010 VASCHETTO-5 per mille 2010 MIUR, Fondazione Piemontese per la Ricerca sulla Cancro- ONLUS.
VL received a fellowship by MIUR (University of Turin); GM and LG were sponsored by the ‘Associazione Italiana Ricerca sul Cancro–AIRC’ FM, PL and VL received support from the Fondazione Umberto Veronesi.
Limited financial contribution was provided by Celgene.
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