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EV-associated miRNAs from peritoneal lavage as potential diagnostic biomarkers in colorectal cancer
Journal of Translational Medicinevolume 17, Article number: 208 (2019)
Colorectal cancer (CRC) is the third leading cause of cancer-related mortality worldwide. Current systematic methods for diagnosing have inherent limitations so development of a minimally-invasive diagnosis, based on the identification of sensitive biomarkers in liquid biopsies could therefore facilitate screening among population at risk.
In this study, we aim to develop a novel approach to identify highly sensitive and specific biomarkers by investigating the use of extracellular vesicles (EVs) isolated from the peritoneal lavage as a source of potential miRNA diagnostic biomarkers. We isolated EVs by ultracentrifugation from 25 ascitic fluids and 25 peritoneal lavages from non-cancer and CRC patients, respectively. Analysis of the expression of EV-associated miRNAs was performed using Taqman OpenArray technology through which we could detect 371 miRNAs.
210 miRNAs were significantly dysregulated (adjusted p value < 0.05 and abs(logFC) ≥ 1). The top-10 miRNAs, which had the AUC value higher than 0.95, were miRNA-199b-5p, miRNA-150-5p, miRNA-29c-5p, miRNA-218-5p, miRNA-99a-3p, miRNA-383-5p, miRNA-199a-3p, miRNA-193a-5p, miRNA-10b-5p and miRNA-181c-5p.
This finding opens the avenue to the use of EV-associated miRNA of peritoneal lavages as an untapped source of biomarkers for CRC.
Colorectal cancer (CRC) is the third most common type of malignant tumor and the third leading cause of cancer-related mortality worldwide among men and women . The overall survival of colorectal cancer is 65%, but this is highly dependent upon the disease stage at diagnosis, and ranges from a 90% of 5-year survival rate for cancers detected at the localized stage (40% of the cases) and 70% for regional (35% of the cases) to 15% for distant metastatic cancer (20% of the cases) . Current systematic methods for diagnosis, such as fecal occult blood test and flexible sigmoidoscopy, help to reduce mortality by removing precursor lesions and making diagnosis at an earlier stage. However, these techniques have inherent limitations, such as low sensitivity and invasiveness for patients, respectively; and the burden of disease and mortality is still high . Serum tumor markers CA19-9 and CEA have been used for detection of many types of cancer, but their sensitivity for the detection of CRC is low . Therefore, development of a minimally-invasive diagnosis, based on the identification of sensitive biomarkers in liquid biopsies could therefore facilitate screening among population at risk of CRC, impact on early detection, and thus, decrease CRC-related mortality.
MiRNAs are a highly conserved family of endogenous non-coding and single-stranded RNAs that are 19–24 nucleotides in length . Generally, miRNAs negatively regulate gene expression via binding to the 3′-untranslated region (3′-UTR) of their target double-stranded mRNA that results in transcriptional repression or mRNA degradation upon dicer complex . miRNAs have been implicated in development and progression of CRC by functioning as oncogenes and tumor suppressors . Recent studies demonstrated that miRNAs are secreted from various cells, including cancer cells, into bodily fluids such as blood, urine, breast milk, and saliva, either as free miRNAs or via extracellular vesicles (EVs) .
EVs are 20–200 nm membrane vesicles released by either directly from plasma membranes, or from intracellular multivesicular bodies by their fusion with the cell membrane. Their function is to mediate intercellular communication, influencing the recipient cell function. Importantly, EVs have awakened the interest of the scientific community as a source of biomarkers, mainly because they carry a broad range of bioactive material (proteins, metabolites, RNA, miRNA, etc.) and this material is well-protected owing to the EVs lipid bilayer membrane, even if EVs are extracted from circulating or proximal body fluids .
Herein, we investigated the use of EVs isolated from the peritoneal lavage, a proximal fluid in CRC patients, as a source of potential diagnostic biomarkers. To do so, we conducted miRNA-profiling of EVs isolated from peritoneal lavages of surgical CRC patients and ascitic fluids of non-cancer patients by using the TaqMan OpenArray Human MicroRNA Panel. We unveiled the most relevant individual miRNAs for diagnosing CRC and characterized the biological and molecular landscape of the CRC milieu. The study was conceived as a proof of concept investigation to demonstrate the feasibility of peritoneal lavage as a source of EV-associated miRNAs in patients with CRC.
Patients and ascitic fluid and peritoneal lavages collection
Participants in the study attended to the Hospital Arnau de Vilanova in Lleida, Spain. The Clinical Research Ethics Committee of the hospital approved the study and all the participating patients provided a signed informed consent. Ascitic fluids and peritoneal lavages were extracted from a cohort of 50 patients, corresponding to 25 control patients with decompensated cirrhosis, and 25 patients with CRC who underwent curative surgery. In control patients, the collection of ascitic fluid was aspirated using 18 or 21G needles (for diagnostic paracentesis) or an over-the-needle catheter device (for therapeutic paracentesis). The procedure was performed under sterile conditions, the site of needle insertion was selected by ultrasound guidance, and skin and parietal peritoneum were previously anesthetized with 2% mepivacine. A total of 100 mL of ascitic fluid was gently aspirated, collected into a 50 mL tube and stored at − 80 °C. In CRC patients, the collection of peritoneal lavage was performed before the surgery, once the abdominal cavity has been opened and prior to any manipulation of the colon. A total of 100 mL of physiological saline were instilled into the abdominal cavity with a 50 mL syringe, mobilizing patients for the correct distribution of saline, which was then extracted with a 50 mL syringe connected to a 14-gauge aspiration needle. The peritoneal lavage was gently aspirated. A volume ranging from 50 to 100 mL was collected and stored at − 80 °C. The clinical features of each patient are listed in Additional file 1: Table S1.
EVs were isolated with a differential centrifugation method as previously described  with slight modifications. Briefly, ascitic fluids and peritoneal lavages were centrifuged at 300×g for 10 min, followed by a centrifugation at 2500×g for 20 min and a centrifugation of 10,000g for 30 min (Thermo Scientific Heraeus MultifugeX3R Centrifuge (FiberLite rotor F15-8x-50c)). The supernatant was then filtered through 0.22 µm filters (Merck Millipore) and the sample obtained was transferred to ultracentrifuge tubes (Beckman Coulter) and filled with PBS to perform two consecutive ultracentrifugation steps at 100,000g for 2 h each on a Thermo Scientific Sorvall WX UltraSeries Centrifuge with an AH-629 rotor. The pellet containing the EVs was resuspended in 50 µL of PBS. From those, 5 µL were isolated for nanoparticle tracking analysis (NTA) and quantification, and the rest was frozen at − 80 °C with 500 µL of Qiazol for RNA extraction.
Nanoparticle tracking analysis
Size and number of EVs was determined using a Nanosight LM10 instrument equipped with a 405 nm laser and a Hamamatsu C11440 ORCA-Flash 2.8 camera (Hamamatsu) with Nanoparticle Tracking Analysis (NTA, Malvern Instruments, UK). Each sample was diluted appropriately with Milli-Q water (Milli-Q Synthesis, Merck Millipore, Massachusetts, USA) to give counts in the linear range of the instrument. The particles in the laser beam undergo Brownian motion, and a video was recorded for 60 s in triplicate. Analysis was performed following manufacturer’s instructions and data were analyzed using the version 2.3 of the NTA-software.
Total RNA extraction and OpenArray analysis
Total RNA, including miRNAs and other RNAs, was isolated from the EVs samples using the miRNeasy MiniKit (Qiagen) according to manufacturer’s protocol. RNA from EVs was eluted with 30 µL of Nuclease-free water (Ambion). MiRNA expression was performed using TaqMan OpenArray Human MicroRNA Panel, QuantStudio 12 K Flex (Catalog number: 4470187, Thermo Fisher Scientific), a fixed-content panel containing 754 well-characterized human miRNA sequences from the Sanger miRBase v14 and according to the manufacturer’s instructions. Reverse transcription (RT) was performed on 2 µL RNA using Megaplex™ Primer Pools A and B and the supporting TaqMan® MicroRNA Reverse Transcription Kit as follows: 15 min at 42 °C and 5 min at 85 °C. Then, 5 µL of the resulting cDNA was preamplified prior to real-time PCR analysis using Megaplex™ PreAmp Pools and the TaqMan® PreAmp Master Mix using the following conditions: one single step at 95 °C during 5 min, 20 cycles of a two-steps program (3 s, 95 °C and 30 s, 60 °C) followed by a single cycle of 10 min at 99 °C to inactivate the enzyme. The preamplified products were diluted 1:20 in 0.1× TE buffer pH8.0, and mixed in 1:1 with TaqMan® OpenArray® Real-Time PCR Master Mix in the 384-well OpenArray® Sample Loading Plate. TaqMan® OpenArray® MicroRNA Panels were automatically loaded using the AccuFill™ System.
Preprocessing and differential expression analysis
All bioinformatics analysis was performed with the BioConductor (version 3.7)  project in the R statistical environment (version 3.5.0) . For the data preprocessing, the HTqPCR (version 1.34) R package  was used. Probes that had a “Cycle threshold” (Ct) value of 40 in all samples were removed. Further samples in which more than 80% of the probes had a Ct value above 40 were retained. To assure comparability across samples, the Ct values were delta normalized. The average Ct values of the probes hsa − miR − 150 − 5p, hsa − let − 7g-5p, hsa − miR − 598 − 3p, and hsa − miR − 361 − 3p were used for normalization. These probes had the Ct values of 40 in a maximum of three samples, and the lowest interquartile range across samples. Differential expression analysis was carried out with an empirical Bayes approach on linear models, using the limma (version 3.36) R Package . Results were corrected for multiple testing using the False Discovery Rate (FDR) .
Development of predictors
For predictive analysis, the whole patient cohort was randomly divided into training and validation sets with the 3:2 ratio. Calculated (with the limma R Package) relative miRNA expression values were used as input variables to a logistic regression model between groups. Each miRNA (adjusted p-value < 0.05) was fitted in the logistic regression model to differentiate the CRC and the control patients groups in the training set and its classification ability was evaluated using the AUC (area under the ROC curve), accuracy, sensitivity, and specificity values on the validation set. The procedure from division into training and validation sets and fitting the logistic model was repeated 500 times and statistics were collected.
miRNA target genes prediction and bioinformatics analysis
miRNAs target genes were obtained using the Predictive Target Module of miRWalk2.0 online software  (https://goo.gl/ajG9ja), considering the following parameters: 3´UTR localization, miRNA seed start at position 1 and minimum 7 bp seed length. To improve the accuracy of target gene prediction, only those transcripts that were predicted in at least 8 out of the 12 databases were considered (miRWalk, miRanda, MicroT4, miRDB, miRMap, miRBridge, miRNAMap, PICTAR2, RNA22, PITA, TargetScan, and RNAhybrid). Gene Ontology (GO) functional analysis were used to analyze the potential functions of the predicted target genes, using the online Panther software  (http://www.pantherdb.org/). Biological process (BP) and molecular function (MF) GO terms were analyzed and plotted.
We analyzed the miRNA profile of EVs isolated from the ascitic fluid of 25 control individuals and peritoneal lavage of 25 CRC patients. Additional file 2: Figure S1 illustrates the workflow that was followed in this study. The quality of EVs isolated from the ascitic fluids and peritoneal lavages was measured by size distribution and concentration by Nanoparticle Tracking Analysis, demonstrating that we analyzed a population mostly enriched in small EVs but also containing a low representation of larger vesicles (Additional file 3: Figure S2). MiRNAs were extracted from EVs for a systematic miRNA expression analysis using the Taqman OpenArray technology, through which we detected 371 out of the 754 miRNAs (49.2%) present in the OpenArray. Probes that had the Ct value of 40 in all samples and samples in which more than 80% of the probes had the Ct value above 40 were removed, resulting in 355 miRNAs from 22 control and 19 CRC patients analyzed for the differential expression analysis (Table 1).
The differential expression analysis between cancer and control cases yielded a list of 210 miRNAs that were significantly dysregulated (adj. p-value < 0.05 and logFC lower or higher than 1). Among those, 207 miRNA were found to be downregulated and 3 miRNA were upregulated in CRC patients. To evaluate whether these miRNAs can be used as diagnostics biomarkers, we performed a predictive analysis using the logistic modeling. Ten miRNAs demonstrated predictive performance at the AUC values higher than 0.95: miRNA-199b-5p, miRNA-150-5p, miRNA-29c-5p, miRNA-218-5p, miRNA-99a-3p, miRNA-383-5p, miRNA-199a-3p, miRNA-193a-5p, miRNA-10b-5p and miRNA-181c-5p (Table 2; Fig. 1). All those miRNAs were downregulated from 3.52 to 12.82 in the log2 scale with adjusted p-value lower than 1.56E−05, except miRNA-150-5p which was upregulated (adjusted p-value 3.41E−04). In Table 3, studies reporting an association between each of these top-10 miRNAs and CRC are described based on a search of Pubmed for each miRNA and the word “colorectal cancer”. Although there are some controversies among the different studies, most of the miRNA dysregulations observed in our study are concordant with the observations reported by other authors, either in tissue, plasma or stool samples. MiRNA-199b-5p, miRNA-29c-5p, and miRNA-99a-3p have never been reported previously in association to CRC.
To further understand the milieu generated by CRC EVs, we performed a bioinformatics study to first unveil the predicted transcripts that are regulated by all the differential miRNAs, and then assess the biological processes and molecular functions in which they participate. A total of 9358 transcripts were found to be regulated by the 210 miRNA differentially expressed. Figure 2 shows the number and most frequently regulated transcripts predicted for each dysregulated miRNA. To comprehensively integrate the properties of all target transcripts, they were studied using Gene Ontology (GO). The most enriched biological processes in CRC EVs were metabolic processes (24.3%), mostly including biosynthetic process, organic substance metabolomic process and cellular metabolic process; biological regulation (22.5%); cellular processes (10.7%), signal transduction, cellular component organization and cellular metabolic process; and cellular component organization or biogenesis, including cellular component organization (Fig. 3a). In relation to the most altered molecular functions in CRC EVs, the Gene Ontology (GO) analysis revealed that many targeted transcripts were found to be involved in binding (37.8%), including protein binding and organic cyclic compound binding; and in catalytic activity (31.2%), including catalytic activity, and protein and hydrolase activity (Fig. 3b).
In this study we investigated, for the first time, the miRNA content of EVs isolated from peritoneal lavages and ascitic liquid of CRC and control patients, respectively. Our study shows that EV-associated miRNAs can be consistently extracted from peritoneal lavages and ascitic liquids and that miRNA expression profiles can indicate and represent the status of CRC patients. The EV-associated miRNA were analyzed by Taqman OpenArray technology and the differential expression analysis yielded a list of 210 miRNAs that were significantly dysregulated in CRC patients, being downregulated the 98.57% of the altered miRNAs.
The finding that miRNAs are dysregulated in CRC patients is known, as many studies have reported this previously, mostly in tissue specimens  but also in different body fluids. In CRC, most of the studies use plasma or serum as it is the most common, easy-to-handle, accessible liquid biopsy. The first report detected 69 miRNAs in serum of CRC patients but not in serum of normal controls . Since then, several studies have identified miRNA upregulation or downregulation in plasma or serum samples  including studies that have focus on the search of biomarkers in miRNAs dysregulated in the vesicular fraction of the serum or plasma of CRC patients. Hiroko Ogata-Kawata et al.  analyzed the EV-associated miRNA profile of serum samples from CRC patients and healthy controls and identified 16 miRNA that were expressed in a significantly higher levels among CRC patients. Of these, 7 miRNAs (let-7a, miR-1229, miR-1246, miR-150, miR-21, miR-223, and miR-23a) were suggested as promising diagnostic biomarkers of CRC with an AUC between 0.67 and 0.95. More recently, the serum exosomal miRNA-19a was found to be upregulated in the serum of CRC patients compared to healthy volunteers, but also was associated with poor prognosis . Finally, Zhao et al. , demonstrated that the exosomal miRNA-21 expression is associated with the early diagnosis of CRC. Although plasma and serum have reported promising biomarkers for CRC diagnosis, other approaches as it is the use of proximal bodily fluids as a source of biomarkers have aroused the attention of the biomarker research community. Proximal bodily fluids, such as urine for prostate cancer , or uterine fluid for endometrial cancer  have demonstrated that this type of fluids offers an improved representation of the molecular alterations that takes place in the tumor. The peritoneal lavage is a proximal fluid with an unexploded value in biomarker research for cancers originating within the peritoneal cavity. Tokuhisa et al.  showed that EV-associated miRNAs can be consistently extracted from this bodily fluid and that miRNAs expression profiles can indicate the status of peritoneum in gastric cancer patients.
To the best of our knowledge, our study is the first to report the value of this proximal fluid for the identification of miRNAs associated to EVs in CRC. Importantly, this study unveiled the promising use of the top-10 miRNA dysregulated (miRNA-199b-5p, miRNA-150-5p, miRNA-29c-5p, miRNA-218-5p, miRNA-99a-3p, miRNA-383-5p, miRNA-199a-3p, miRNA-193a-5p, miRNA-10b-5p and miRNA-181c-5p) as diagnostic biomarkers, all showing the AUC value higher than 0.95. Those biomarkers should be validated as well as combined in order to increase the already excellent accuracy of individual miRNAs. However, this should be done in an independent study including a larger cohort of patients. Moreover, further analysis should be performed to elucidate the prognostic value of the detection of the different types of miRNAs in EVs isolated from peritoneal lavages.
In this study, we have demonstrated that use of EV-associated miRNA of ascitic liquid from control patients and peritoneal lavages from CRC patients are an untapped source of biomarkers. Specifically, we identified miRNA-199b-5p, miRNA-150-5p, miRNA-29c-5p, miRNA-218-5p, miRNA-99a-3p, miRNA-383-5p, miRNA-199a-3p, miRNA-193a-5p, miRNA-10b-5p and miRNA-181c-5p as promising biomarkers of CRC diagnosis with the AUC value higher than 0.95.
Availability of data and materials
All bioinformatics analysis was performed with the BioConductor (version 3.7)  project in the R statistical environment (version 3.5.0).
False Discovery Rate
area under the ROC curve
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The authors would like to acknowledge the work of all who have participated in the recruitment of clinical samples. We also thank the patients for their willingness to participate in the study.
EC hold a postdoctoral fellowship from the Departament de Salut of the Generalitat de Catalunya (SLT002/16/00274). This work was supported by grants: Discovery, validation and implementation of biomarkers for Precision Oncology (ISCIII PIE15/00029), CIBERONC (CB16/12/00231 and CB16/12/00328). Grups consolidats de la Generalitat de Catalunya (2017SGR1368 and 2017SGR1661). Work supported by IRBLleida BIOBANK (B.0000682) and Plataforma biobancos PT17/0015/0027.
Ethics approval and consent to participate
Participants in the study attended to the Hospital Arnau de Vilanova in Lleida, Spain. The Clinical Research Ethics Committee of the hospital approved the study and all the participating patients provided a signed informed consent.
Consent for publication
All authors consent for publication.
The authors declare that they have no competing interests.
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