Detection and quantif cation of extracellular microRNAs in medulloblastoma

Department of Oncology, University Children’s Hospital Zurich, 803 Zurich, Switzerland.

2Department of Biology, PartnerChip CEA, Génopole Campus 2, 91000 évry, France.

Detection and quantif cation of extracellular microRNAs in medulloblastoma

Tarek Shalaby1, Giulio Fiaschetti1, Sylvain Baulande2, Nicolas U. Gerber1, Martin Baumgartner1, Michael A. Grotzer1
1Department of Oncology, University Children’s Hospital Zurich, 8032 Zurich, Switzerland.

2Department of Biology, PartnerChip CEA, Génopole Campus 2, 91000 évry, France.

Aim: Medu lloblastoma (MB) is the most common malignant brain tumor in children. The crucial role of extracellular-microRNAs (ex-miRNAs) in cancer has been widely recognized; however, their role in MB remains unknown. This study aimed to investigate MB-driven ex-miRNAs. Methods: Microarray analysis was used to disclose the identity and quantity of key miRNAs excreted in culture-medium (CM) of 3 human MB cell lines and cere brospinal f uid (CSF) of brain tumors (including MB) and leukemia patients. MiRNA expression was validated by quantitative reverse transcription polymerase chain reaction. Results: We have demonstrated that the 3 MB cell lines tested commonly expressed 1,083 miRNAs in their spent CM. Among them, 57 miRNAs were specif c to the CM of metastasis-related cell lines which represents the aggressive group 3 and group 4 MB subtypes. A signif cant number (1,254) of ex-miRNAs were identif ed in the CSF of a MB patient. Eighty-six of these miRNAs were found to be differentially expressed in this patient’s CSF compared with controls. Interestingly, 3 metastasis-associated miRNAs over-represented in CM of metastasis-related MB cell lines were found to be signif cantly enriched in the CSF of the MB patient. Conclusion: Although more samples are required to fully verify these results, our work provides the f rst evidence for the presence of a signif cant amount of miRNAs excreted extracellularly by MB cells and raises the possibility that, in the near future, miRNAs could be probed in CSF of MB patients and serve as novel biological markers.

Medulloblastoma, extracellular-microRNA, pediatric cancer

Ⅰntroduction

Medulloblastoma (MB) is the most common malignant brain tumor in children.[1]Metastatic MB carries a poor prognosis.[2]Mechanisms that predict dissemination are poorly understood. Recently, several studies have revealed a critical role for microRNAs (miRNAs) during tumorigenesis and metastasis of several cancers, including MB.[3-6]

Besides intracellular miRNAs with the traditional function of translation regulation, there is accumulating evidence that miRNAs exist extracellularly in body f uids, including cerebrospinal f uids (CSF).[7,8]Several reports have described that deregulated extracellular-miRNAs (ex-miRNAs) are closely associated with the clinical course of malignant tumors.[9,10]Interestingly, such deregulation returns to a normal level after tumor resection.[7,8]Hence, expression analysis of ex-miRNAs is of increasing interest for diagnostic and prognostic purposes. Every cancer investigated has a distinct miRNA signature and deregulated levels of miRNAs have been detected in body f uids of patients, including those with lymphoma,[11]leukemia,[12]colon,[13]breast,[14]prostate,[15]ovarian,[16]pancreatic,[17]gastric,[18]and lung cancer.[19]In the context of brain tumors, recent studies have demonstrated a signif cant presence of certain miRNAs in CSF samples from patients with central nervous system lymphoma, glioma, and metastatic brain cancers.[20-22]Recent miRNA prof ling of CSF has enabled early detection of glioblastoma and ref ected disease activity.[22]Therefore, ex-miRNAs may represent important minimally invasive candidate biomarkers in brain tumors. The presence and biological role of ex-miRNAs in MBs, however, remain unknown. This study was conducted to gain insight into the identity and quantity of MB-related ex-miRNAs and to speculate on their possible biological function in the context of MB metastasis.

Methods

Patient characteristics and CSF

CSF samples from patients with MB (n = 2), control patients with leukemia with no intracranial mass lesions and/or neurologic disorders (n = 3), CSF samples from patients with ependymoma (n = 3) and glioblastoma (n = 1) that were collected from patients treated at the University Children’s Hospital of Zürich,Switzerland. Written informed consent was obtained from each patient. CSF samples from patients with MB were collected 3 weeks after surgery and before start of radiotherapy or chemotherapy. CSF samples were centrifuged (500 g, 10 min, room temperature) within 60 min after collection to remove cells and debris and were stored at -80 °C until further processing.

Human MB cell lines

Human MB cell lines (DAOY and D283) were purchased from American Type Culture Collection (Manassas, VA, USA). D341 human MB cells were the kind gift of Dr. Henry Friedman (Duke University, Durham, UK). MB cell lines were cultured as previously published[23]and maintained at 37 °C in a humidif ed atmosphere with 5% CO2. To isolate RNA from cultured medium, 10.000-20.000/mL DAOY cells or 20.000-40.000/mL D341, D283, and T293 cells were plated and left to grow in their conditioned media for 72 h in 24 wells plates. Conditioned medium (2 mL) of each cell lines were centrifuged at 1,200 rpm to remove cells. The supernatant was then centrifuged at 10,000 rpm to remove debris.

RNA extraction for microarray

Total RNA from cell cultures or CSF were extracted using a mix of Qiazol, Qiagen (Qiagen, Basel, Switzerland) and chloroform directly on cells. For small RNA in conditioned medium or CSF, the addition of miRNAs extraction reagent (Toray) was performed. In both situations, a centrifugation step was required to collect aqueous phase containing RNA that was f nally transferred to miRNeasy Mini spin column from miRNeasy purif cation kit Qiagen (Qiagen, Basel, Switzerland). After subsequent washing steps, RNAs were eluted using 30 μL of nuclease-free water and concentrated up to 3 μL with vacuum concentrator. Quality was checked on Bioanalyzer using RNA 6000 Pico Chip (Agilent Chemical Analysis, Life Sciences, and Diagnostics. Basel, Switzerland) gel and quantif ed using Nanodrop Photometer [Figure 1a and b].

Labeling and hybridization

Total RNA (250 ng) extracted from cells and 3 μL of concentrated small RNA extracted from medium were used with Toray 3D-Gene miRNA labeling kit (Toray, Japan) in presence of spikes used as positive controls. Brief y, 5’-phosphates were removed from miRNA end using alkaline phosphatase and a f uorescent label was enzymatically attached to the 3’-end of the miRNA. After an enzyme inactivation step and addition of a hybridization buffer, labeled miRNA was injected on 3D-Gene Human miRNA Oligo Chips (Toray, Japan) targeting 2019 miRNA based on miRBase release 19. Finally, arrays were placed in a hybridization chamber and set into a 32 °C oven for 16 h with a shaker adjusted to 250 rpm.

Washing and scanning

Arrays were washed using 3 solutions with different stringencies to remove non-specif cally bound miRNAs. Then, arrays were scanned with the 3D-Gene Scanner 3000 instrument (Toray, Japan) to measure f uorescence. Scanning was carried out using 3 different photomultiplier sensitivities (PMT gain) to allow optimizing of signal detection and checking for consistency.

Microarray analysis

Images were analyzed with the 3D-Gene Extraction software (Toray, Japan). After completion of the auto-analysis work followed on image f les, raw signals, and detection calls was produced in tabular f les. GeneSpring GX12 (Agilent) was then used to apply quantile normalization and differential expression analysis using modif ed t-test implemented in the software. Experimental variability was assessed with principal component analysis (PCA) [Figures 2 and 3b] and Pearson correlat ion matrix [Figure 3a] generated using the same software.

Figure 1: Quality control for RNA isolated from CSF, cell lines, and their corresponding CM measured/analyzed by (a) BioAnalyzer PicoChip (Agilent); (b) RNA gel. CM: Culture-medium; CSF: Cerebral spinal f uid

Figure 2: PCA graph showing microRNA spectra in CSF of MB patient vs. control CSFs. TB0021_CTR1: CSF from patient with no brain tumor control 1; TB0012_CTR2: CSF from patient with no brain tumor control 2; TB0011_ MB: CSF of MB patient. MB: Medulloblastoma; CSF: cerebral spinal f uid; PCA: Principal component analysis

MicroRNA isolation for reverse transcription polymerase chain reaction analysis

For precipitation of nucleic acids, the monovalent cation concentration of the solution was adjusted to 0.5 mol/L sodium acetate. Glycogen (AM9510, Ambion, Life Technology, NY, USA) was added to a final concentration of 100 μg/mL. The solution was then mixed with 1 volume of isopropanol. The mixture was chilled for 20 min at -20 °C, then centrifuged for 20 min at 13,000 rpm. The supernatant fluid was removed, and the nucleic acid resuspended in lysis buffer. Final purification of RNA enriched for small RNAs from 600 μL of conditioned media and CSF samples was obtained using the mirVanaTM miRNA Isolation Kit (Ambion, Life Technology) according to manufacturer’s instructions for “Enrichment Procedure for Small RNAs.” Using this approach consisting of two sequential filtrations with different ethanol concentrations, an RNA fraction highly enriched in RNA species ≤ 200 nt was obtained. First strand synthesis of mature miRNAs was followed by quantitative reverse transcription polymerase chain reaction (qRT-PCR) using miRNA-specific TaqMan MGB probes (Applied Biosystems, Life Technology). For the qRT-PCR reaction, the Gene Expression Master Mix was used and the protocol was optimized for the ABI7900HT reader (Applied Biosystems). Probe-primer solutions specific for the following miRNAs were used: miR-1290 (002863), miR-125a-3p (002199), miR-1298 (002861), miR-125b-1* (002378), miR-486-3p (002093), miR-572 (001614), miR-4476 (464702_mat), miR-615-5p (002353), and miR-3918 (464506_mat) (Applied Biosystems, Life Technology). The relative gene expression was calculated for each gene of interest using the ΔΔCT method, where cycle threshold values were normalized to the level of cel-miR-39-3p (4464066,

Ambion, Life Technology), which was used as spike-in by adding it during the lysis step of miRNAs extraction.

Results

Detection of ex-miRNAs in cultured medium of MB cell lines by microarray analysis

Given that some human cancer cells secrete miRNAs into their extracellular environment and body f uids,[24-26]it was hypothesized that MB cell lines may secrete miRNAs into their spent culture medium. To test this hypothesis, 3 cell lines representing MB subtypes D341 and D283 (metastasis-related group 3 and group 4 MB subtypes)[27]and DAOY (sonic hedgehog-related) were cultured individually for 72 h in vitro and miRNAs expression was analyzed in the lysates of each MB cell line and in their corresponding culture media. We identif ed 1,662, 1,615, and 1,199 secreted miRNAs in the culture-medium (CM) of MB cell lines D283, D341 and DAOY, respectively, among them 1,083 miRNAs that were common in the CM of the 3 cell lines. In cell lysates of D283, D341 and DAOY, on the other hand, we detected 1,787, 1,394 and 1,761 miRNA respectively, with 1,347 miRNAs found common to all 3 cell lines [Figure 4a]. Interestingly, 950 miRNAs were commonly identif ed in CM of both groups and in lysates of the 3 cell lines tested, indicating that the level of ex-miRNAs may well ref ect the expression level of tumor miRNAs. Using a fold-change > 2, we identif ed a group of 156 miRNAs that are commonly enriched in CM derived from the 3 cell lines compared to their respective cell lysates [Figure 4b] and [Supplementary Table 1] and 57 miRNAs that were spec if c to the CM of D341 and D283, which represented the 2 metastasis-related group 3 and group 4 MB subtypes, respectively[27]compared to DAOY-derived CM [Figure 4b] and [Supplementary Table 2]. We found 2 additional groups of miRNAs to be differentially enriched in CM of D341 and D283, represented by 60 miRNAs overrepresented and 52 underrepresented compared to DAOY-derived CM [Supplementary Tables 3 and 4]. Overall, the results of this experiment demonstrate that MB cell lines secrete miRNAs into the CM and that certain ex-miRNAs retain different enrichment levels in the CM-derived from the 2 cell lines representing the metastasis-related group 3 and group 4 MB subtypes

Detection of ex-miRNAs in CSF of MB patients by microarray analysis

Figure 3: (a) Pearson correlation analysis for indicated samples; (b) PCA graph representing microRNA spectra inside MB cell lines (cell line name-C), in culture medium (cell line name-M) and in CSF of MB patient (TB0011-MB) compared to control TB0021_CTR1 and TB0012_CTR2. Graph demonstrating similarity between miRNA prof le in CM and those secreted in CSF of MB patient. CM: Culture medium; PCA: Principal component analysis; MB: Medulloblastoma; CSF: Cerebral spinal f uid

We next asked whether ex-miRNAs could be detected in CSF of MB patients, to test whether it would be technically possible to use the CSF as a source for diagnostic miRNA testing. Using microarray analysis, we screened cell-free CSF from a patient with MB and compared the results to controls (CSF from two different leukemia patients with no cerebral manifestation or neurological disease). PCA [Figure 2] showed clear separation between the miRNA spectrum in CSF of MB patient and controls. Microarray analysis identif ed 1,254 miRNAs in the MB-CSF sample [Table 1], of which 86 miRNAs were differentially expressed in CSF of the MB patient compared to the 2 CSF controls [Figure 4c] and [Supplementary Table 5]. Further analysis identif ed 268 miRNAs over-represented (with fold-change > 2) and 6 miRNAs under-represented in MB-CSF compared with the 2 different controls tested [Supplementary Tables 6 and 7], indicating a trend toward miRNA enrichment in the MB-CSF sample.

Figure 4: MiRNAs expression spectrum in MB cell lines, their corresponding CM and in CSF (a) Quantitative Venn diagram showing miRNAs commonly expressed in indicated cell lines and their corresponding CM. Differences linked to the expression level rather than detection threshold; (b) Venn diagram showing that 156 miRNAs enriched in CM of MB cell lines compared to their cell lysates and 57 miRNAs enriched in CM of the MR D283 and D341 but not in DAOY. Fold change > 2; (c) Venn diagram demonstrating miRNAs with high expression in CSF of MB patient compared to controls. TB0021_CTR1: CSF of leukemia with no brain tumor (patient control 1); TB0012_CTR2: leukemia with no brain tumor (patient control 2); TB0011_MB: CSF of MB patient. MB: Medulloblastoma; CSF: Cerebral spinal f uid; CM: Culture-medium; MiRNAs: MicroRNAs

Table 1: Number of miRNAs detected in CSF

Comparison between miRNA expressions in CM vs. CSF samples

An overlap of the spectra of ex-miRNA candidates detected in the CSF of the MB patient and those excreted by MB cell lines into the CM would support our hypothesis of miRNA secretion by MB cells. Indeed, Pearson correlations analysis showed that ex-miRNAs prof les in MB-CSF displayed a good homogeneity with the prof le of miRNAs secreted in CM of MB cell lines [Figure 3a]. This conclusion was conf rmed by PCA showing clear separation of miRNAs derived from lysates of MB cell lines from those derived of MB-CSF samples or of CM derived from MB cells [Figure 3b], conf rming the conclusions from Pearson correlations. Compiling expression tables allowed identif cation of 5 miRNAs (miR-486-3p, miR-572, miR-3918, miR-4476, and miR-615) that were signif cantly up-regulated in the CM of the 3 cell lines (D283, D341 and DAOY) and enriched in MB-CSF compared to control CSF [Figure 5a]. Moreover, 3 other miRNAs (miR-1290, miR-125a, miR-125b), known to be associated with metastasis, and miR-1298, were over-represented in the CM of metastasis-related cell lines (D283 and D341), but not in DAOY and were signif cantly over-represented in MB-CSF compared to control CSF [Figure 5b].

Validation of microarray data by qRT-PCR

In order to further verify the results of miRNA microarray analysis, we selected miR-486-3p, miR-572, miR-3918, miR-4476, and miR-615 for quantitative real-time PCR assays because of their over-representation in the CM of the 3 MB cell lines and in MB-CSF. TaqMan analysis conf rmed the outcomes of miRNA microarray prof ling for the 5 miRNAs tested and showed that the f ve were enriched in the CM of the 3 cell lines [Figure 6a]. However, only miR-615 and miR-572 were also accumulated in MB-CSF [Figure 6b]. We also chose miR-1290, miR-125a, miR-125b, and miR-1298 as other candidates for qRT-PCR due to their over-representation in CM of metastasis-related cell lines D283 and D341, as well as in CSF of the MB patients. TaqMan analysis showed an evidently increased expression level of the 4 cell line-derived miRNAs in both D283 and D341 compared to DAOY [Figure 7a]. The levels of 3 miRNAs (miR-1290, miR-125a, miR-1298) were also markedly increased in MB-CSF, thus conf rming the results of the miRNA microarray analysis for 3 out of 4 of these selected miRNAs [Figure 7b].

To further validate the f nding of selective enrichment of miR-1298 in MB-CSF, we tested it against an additional 5 different CSF controls from one leukemia patient, 3 ependymoma patients, and one glioblastoma patient (specif cally chosen to control for brain surgery as a possible factor inf uencing miRNA secretion). Consistently, TaqMan analysis conf rmed signif cant enrichment of miR-1298 in MB-CSF compared to the 5 controls [Figure 8a]. Together, using TaqMan analysis, we conf rmed the microarray data result and demonstrated the feasibility of quantitative detection of miRNAs in culture medium and CSF using qRT-PCR (popular gene expression assay and eff cient method for high-throughputused in most diagnostic labs). Importantly, we could detect ex-miRNAs by qRT-PCR in CM of as few as 100-500 MB cells [Figure 8b], recommending qRT-PCR for the development of non-invasive detection of metastasis-predicting markers for MB.

Figure 5: MiRNAs commonly enriched in CM of MB cell lines, and in CSF sample. (a) Venn diagram and table presenting 5 miRNAs commonly upregulated in CM of 3 MB cell lines and in CSF from MB patients compared to CTR; (b) Venn diagram and table representing 4 miRNAs commonly upregulated in CSF samples from MB patients and over-represented in CM of the MR cell lines D341, D283. CM: Culture-medium; MB: Medulloblastoma; CSF: Cerebral spinal f uid; MR: Metastasis related; FC: Fold change; CTR: Control; MiRNAs: MicroRNA

Discussion

Aberrant expression of ex-miRNA circulating in CSF of certain brain tumor patients has recently been reported to be cancer biomarkers and potential regulators of the disease.[7,8]However, the existence and role of ex-miRNAs in MB extracellular environment are unknown. Therefore, better understanding of ex-miRNA secretion and function in MB seems crucial for the development of novel insights for its diagnosis and prognosis. This study aimed to identify key miRNAs in culture medium of 3 cell lines, representing different MB subtypes. Our results identif ed a signif cant number (1,347) of hitherto unrecognized new miRNAs commonly expressed in CM of the 3 cell lines. A signif cant concordance of ex-miRNA spectra in CM and those expressed intracellularly was observed. Since deregulated miRNA expression is an early event in tumorigenesis, measuring miRNA levels in CSF may also be useful for early detection, which can contribute greatly to the success of treatment.[28]Therefore, in order to use ex-miRNAs as biomarkers for MB, it is important to establish a signature capable of differentiating disease from healthy states. Our pilot microarray screening identif ed 86 miRNAs exclusively detected in CSF of MB patients but not in control CSF from patients with no brain tumor. We also identif ed 268 miRNAs that are over-represented and interestingly, only 6 miRNAs under-represented in MB-CSF compared with control CSF. These f ndings could be of great signif cance, providing the correlation between expression levels of these miRNAs in CSF of MB patients and their disease states can be established in future studies.

Tumor cell-derived ex-miRNAs are reported to be pro-tumorigenic.[29]Ex-miRNAs can transfer their oncogenic activity to recipient target cells to inf uence cancer stimulatory activities, thus contributing to the formation of a pre-metastatic niche and promotion of metastasis.[28,30]This exchange of miRNAs between primary tumors and target cells is an interesting and novel dimension to the regulation of a cell phenotype[31-34]and may be particularly important in cancers that have a propensity for dissemination, such as MB. MB includes various subtypes with group 3 and 4 subtypes being clinically distinct with regard to metastasis and prognosis, which may also manifest in a difference in their miRNA spectra. Hence, it was not surprising to f nd a group of miRNAs that were uniquely over-(60 miRNAs) or under-represented (52 miRNAs) in the CM of the 2 metastasis-related cell lines D283 and D341. More importantly, we identif ed 4 miRNAs (miR-1290, miR-125a, miR-125b, miR-1298) that were over-represented in MB CSF and signif cantly enriched in the CM media of the 2 metastasis-related cell lines (D283 and D341). Remarkably, apart from miR-1298, where no functional information is publically available, the 3 other miRNAs (miR-1290, miR-125a, miR-125b) were detected in body f uids of various cancer patients, whereby their increased expression and/or secretion is associated with metastasis of multiple malignancies.[35-39]Consistently, detection of metastasis-related ex-miRNAs in extracellular environment of certain human malignancies, including breast and prostate cancers, were observed in other studies.[40-44]Our observations provide indirect evidence supporting the hypothesis that ex-miRNA are possible facilitators of metastasis by modifying local or distal microenvironments.[45]However, further studies are needed using counter-regulation of key ex-miRNA expression to determine their effect on regulation of motility, migration, and invasion of MB cells.

Figure 7: Expression analysis of 4 overexpressed ex-miRNAs in MB cell lines CM and in CSF of MB patient. (a) TaqMan qRT-PCR analysis for miR-1290, miR-125a, miR-1298, miR-125b in CM of indicated cell lines; (b) TaqMan qRT-PCR analysis for miR-1290, miR-125a, miR-1298 in MB-CSF (n = 3; ± standard deviation). MB: Medulloblastoma; CSF: Cerebral spinal f uid; CM: Culture-medium; qRT-PCR: Quantitative reverse transcription polymerase chain reaction

To the best of our knowledge, this is the f rst study revealing the spectra of ex-miRNAs in cell CM conditioned by MB cell lines and in CSF of an MB patient. Although the number of samples studied here is very small, our identif cation of key secreted miRNAs that are specif cally enriched in MB-CSF provides a rationale for future investigations. Such investigations, using larger sets of MB samples could lead in the near future to the discovery of CSF-derived miRNA markers, with diagnostic and prognostic signif cance and ultimately, hopefully also with therapeutic potential.

Figure 8: Relative ex-microRNAs expression analysis in CSF, MB cell lines: (a) TaqMan qRT-PCR analysis for miR-1298 compared to 5 controls: Ctrl 1 CSF from leukemia patient, Ctrl 2 CSF from glioblastoma patient, Ctrl 3-5 CSF from 3 ependymoma patients (n = 3; ± SD); (b) TaqMan qRT-PCR analysis for miR-1290, miR-125a in serial dilution of D341 CM (n = 3; ± SD). CM: Culture-medium; MB: Medulloblastoma; CSF: Cerebral spinal f uid; qRT-PCR: Quantitative reverse transcription polymerase chain reaction; SD: standard deviation

Acknowledgments

This project was supported by the Swiss Research Foundation Child and Cancer and by “Krebsliga Zürich”.

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How to cite this article:Shalaby T, Fiaschetti G, Baulande S, Gerber NU, Baumgartner M, Grotzer MA. Detection and quantif cation of extracellular microRNAs in medulloblastoma. J Cancer Metastasis Treat 2015;1:67-75.

Received:30-01-2015;Accepted:07-04-2015.

Source of Support:Nil,Conf ict of Interest:None declared.

Prof. Michael A. Grotzer, Department of Oncology, University Children’s Hospital Zurich, Steinwiesstrasse 75CH, 8032 Zurich, Switzerland. E-mail: michael.Grotzer@kispi.uzh.ch

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10.4103/2394-4722.157068