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MicroRNA profile of paclitaxel-resistant serous ovarian carcinoma based on formalin-fixed paraffin-embedded samples
© Li et al.; licensee BioMed Central Ltd. 2013
Received: 27 November 2012
Accepted: 25 April 2013
Published: 30 April 2013
To assess the feasibility of validating microRNA (miRNA) profile related to paclitaxel-sensitivity in formalin-fixed paraffin-embedded (FFPE) samples of serous ovarian carcinoma (OC) patients.
Deregulated miRNAs identified by miRNA microarray were further detected in 45 FFPE OC samples using Realtime PCR. Correlations between paired FFPE and frozen tumor samples were analyzed. Survival times were compared between 6 high and low miRNAs groups. Western blot and luciferase reporter assay were used for validating the target of miRNA.
Sixteen up-regulated miRNAs and twenty-three down-regulated miRNAs were revealed in pacilitaxel-resistant ST30 cells. The up-regulated miRNAs (miR-320a, 22 and 129-5p) and down-regulated miRNAs (miR-9, 155 and 640) were confirmed in paclitaxel-resistant FFPE tumor samples, compared with paclitaxel-sensitive samples. Higher miR-9 and miR-640 showed better survival time in OC patients. Expressions of miR-9, 155 and 22 in FFPE samples were closely mimicked by those in frozen tissues. RAB34 was validated as a direct target of miR-9.
We validated miRNA profile in pacilitaxel-resistant OC using FFPE samples, which might enable treatment stratification and help us to predict outcomes in OC patients. FFPE samples are feasible materials for miRNA research.
Ovarian carcinoma (OC) is the leading cause of death among patients with gynecologic cancer. Despite initial responsiveness to the chemotherapeutic drugs, most patients eventually develop chemoresistance and succumb to their diseases [1, 2]. Drug resistance remains a formidable problem in managing cancer patients. It is clinically important to identify biomarkers that could assist in predicting which patients will respond to chemotherapy, and, which patients will remain refractory to standard treatment.
microRNA (miRNA)s are small noncoding RNAs involved in the initiation and progression of human cancer . As modulators of protein expression they may operate as oncogenes and tumor suppressors . miRNA expression profiles are useful for assessment of the prognosis and chemosensitivity of human cancer. For example, when cisplatin resistance was specifically examined for miRNA expression, 34 miRNAs with statistically significant changes were found in tumors from responders compared with those of non-responders . Among them, Let-7i was the most down-regulated miRNA in the chemo-resistant patients. In another study, elevation of miR-214 was found to be responsible for development of resistance to cisplatin. Blocking miR-214 expression enhanced the sensitivity of A2780 cells to cisplatin-induced apoptosis . Eitan et al. also found an array of tumor specific miRNAs associated with response to platinum . However, few studies have focused on tumor miRNA expression patterns associated with paclitaxel-resistance. Several miRNAs are differentially expressed in paclitaxel-resistant and sensitive OC cell lines, when we detected the miRNAs expressions using miRNA microarray in present study. This raises the question that whether a miRNA profile representing paclitaxel-resistance could be useful for prognosticating clinical chemo-resistance in OC patients.
As we know, routine histology processing uses formalin fixation to preserve clinical specimens, which provides a rich resource of tissues linked to clinical databases. In addition, any biomarker developed from formalin-fixed paraffin embedded (FFPE) samples could be more readily translated into clinical practice than frozen tissues. However, most studies of miRNAs still use frozen tissues, despite prospective collection of frozen samples is limited and inefficient [8, 9]. The most important reason is that RNA is degraded in tissues before, during, and after formalin fixation [10, 11]. Interestingly, miRNAs appear to be better preserved, perhaps because of their shorter lengths. Detecting miRNAs using FFPE tissues has been successful for colon, breast and ovarian cancers [12–14]. In present study, we try to validate a panel of miRNAs associated with pacilitaxel-resistant OC using FFPE samples, and to determine that whether certain miRNAs might predict response to chemotherapy and prognosis. Furthermore, to show the suitability of routine FFPE tissue for comprehensive miRNA expression analyses using Realtime PCR, we also compared expressions of miR-9, 155 and 22 in FFPE samples with those in paired frozen samples from the same patients.
Clinical characteristics of 45 ovarian carcinoma patients
Cases number (N)
Age (range, years)
OS (Range, months)
Cell culture and transfection
Paclitaxel-resistant cell line SKOV3-TR30 (ST30) was induced from SKOV3 (American Type Culture Collection, Manassas, VA, USA). Both were maintained in McCoy’s 5A medium supplemented with 10% fetal bovine serum. For ST30 cells, 30nm paclitaxel was withdrawn at 2 weeks before experiment. For regulation of miR-9, ST30 cells were transfected with 50nM miR-9 mimic or its negative Control (Ribobio, GuangZhou, China) by using Lipofectamine 2000 (Invitrogen, Carlsbad, CA, USA) in accordance with the manufacturer’s instructions.
RNA extraction and microRNA microarray
Total RNA was extracted from 45 FFPE tumor samples and 10 FFPE matched frozen tumor samples from the same patients. For snap-frozen tissues, total RNA was isolated by TRIzol(Invitrogen, California, USA). For FFPE tissues, total RNA was extracted by RecoverAll™ Total Nucleic Acid Isolation Kit (Ambion, Austin, TX, USA), according to the manufacturer’s instructions. Briefly, eight 10-um-thick sections of FFPE samples were deparaffinized with xylene and washed in ethanol. The tissues were digested with protease and treated with DNase. After washing, total RNA was eluted with distilled water. The quantity and quality of RNA were measured by Nanodrop 2000 thermo scientific spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).
miRNA expression profiling of SKOV3 and ST-30 cells were detected using the miRCURY LNA Array (version 11.0) system. RNA samples were labeled with the Exiqon miRCURY™ Hy3™/Hy5™ Power labeling kit and hybridized on the miRCURY LNA Array (version 11.0) station. Scanning was performed with the Axon GenePix 4000B microarray scanner. GenePix pro version 6.0 was used to read image raw intensity of the image. The ratio of red signal to green signal was calculated after background subtraction and normalization using the global Lowess (Locally Weighted Scatter plot Smoothing) regression algorithm (MIDAS, TIGR Microarray Data Analysis System). Between slides normalization was performed by scale normalization to reduce between-slide variability. The experiments were performed in triplicate and repeated three times. The statistical significance of differentially expressed miRNAs was analyzed by fold change and t-test. The threshold value we used to screen differentially expressed miRNAs was a fold change>1.5 or <0.67.
Realtime RT-PCR validation
The most up-regulated and down-regulated miRNAs identified by microarray were further validated in 45 FFPE tumor samples using realtime RT-PCR. To corroborate the validity of miRNAs expression of FFPE samples, three miRNAs were detected in 10 matched FFPE and snap-frozen samples from the same patients. Correlations of miRNAs expressions between matched FFPE and frozen tumor samples were analyzed.
RT reactions and realtime PCR were performed according to the manufacturer’s protocols (TaKaRa, DaLian, China). All RT reactions, including no-template controls were run in a PTC-200 Peltier Thermal Cycler (MJ Research, Waltham, MA, USA). miRNA levels were quantified with the ABI Prism 7900HT sequence detection system (Applied Biosystems, Fostercity, CA, USA). U6 snRNA served as endogenous control. The primers for miRNAs and U6 were obtained from Ribobio (Ribobio, GuangZhou, China). Comparative realtime PCR was performed in triplicate, including no-template controls. Relative expression was calculated using the 2-ΔΔct method.
At 72 h after transfection, total protein extracts from the cells were prepared. Total protein was separated by SDS–PAGE and transferred electrophoretically to a nitrocellulose membrane. The membrane was blocked with 5% nonfat dried milk in TBST buffer, and then incubated overnight at 4°C with primary antibodies against RAB34 (SC-27442, 1:250, Santa Cruz) and GAPDH (sc-25778, 1:1000, Santa Cruz) respectively. Blots were washed with TBST buffer and incubated with secondary antibody. The protein bands were visualized using the EZ-ECL kit (Biological Industries, Kibbutz Beit-Haemek, Israel). GAPDH was used as an endogenous control. The experiments were repeated three times.
Dual luciferase reporter assay
The sequences of primers in the dual luciferase reporter assay
Student’s t-test was used to assess miRNAs expression in FFPE samples and dual luciferase reporter assay. Kaplan-Meier survival functions and log-rank test were used to assess progress-free survival and overall survival time based on mean expression levels of 6 miRNAs. Pearson’s correlation was calculated to compare the PCR results of FFPE samples with those of paired frozen samples. All statistical analyses were two-sided and performed with SPSS 11.5 software package. P-values less than 0.05 were considered statistically significant.
Confirmed paclitaxel-resistant miRNA profile using FFPE samples
Consistent miRNA expressions validated between paired frozen and FFPE samples
To further corroborate the validity of miRNA profile of FFPE samples, realtime RT-PCR were repeated using pairs of frozen and FFPE tissues from the same patients. Correlation analysis of miR-9, 155 and 22 levels in FFPE and frozen samples from the same patients showed significant correlationship of the paired samples, with Pearson’s rho of 0.88, 0.89 and 0.87 respectively (all P= 0.001). Thus, miRNA expression studies can be reliably performed with routinely obtained pathological materials and the results are similar to the yield from snap-frozen tissues.
RAB34 is one of the targets directly regulated by of miR-9
Despite multiple new approaches to treatment, the high death rates from OC remain largely unchanged with a 5-year overall survival of only 30–39% . Dramatically poor prognosis of OC patients is due to the development of chemo-resistance. As shown in Table 1, the median PFS in paclitaxel-sensitive group is 22 months, significantly longer than that in paclitaxel-resistant group (6 months, P=0.000), and the median OS in paclitaxel-sensitive group is also significantly longer than that in paclitaxel-resistant group (42.5 vs 17 months, P=0.000). Therefore, identifying patients who can benefit from the chemotherapy will have significant clinical implications.
miRNA represents a new class of small non-coding RNA that regulates multiple gene expression. During tumorigenesis and tumor progression, up-regulated miRNA could potentially target and down-regulate tumor suppressor genes, whereas down-regulated miRNA could potentially increase the expression of oncogenes . Increasing evidence supports that miRNA may influence the response of ovarian cancer to chemotherapy [17–19]. However, all these evaluations used frozen tissues. In present study, we provide the first characterization of the paclitaxel-resistant miRNA profiling of 45 FFPE samples from primary serous papillary ovarian adenocarcinoma patients using realtime PCR assay. Three top deregulated miRNAs were selected for validation using 10 paired FFPE and frozen samples from the same patients. Importantly, the changes predicted for these 3 miRNAs using the paired samples from the same patients were significantly correlated. Thus, these data demonstrate that FFPE samples may be used as a feasible material for miRNA expression research. Although different types of tumors may have the same miRNAs markers, there are specific miRNAs in tumors from different cellular origins . In present study, the majority of the differentially expressive miRNAs have not been reported before, such as miR-9 and miR-640. This discrepancy may be attributed to different patient population and inter-experimental variations. Our study focused on primary serous papillary ovarian adenocarcinoma patients and paclitaxel-sensitivity, whereas previous studies were involved different histological types of ovarian cancer and chemotherapy agents [5–7].
Specific data may assist in tailoring treatment to each patient’s specific clinical situation during the initial management of their disease and also offer the opportunity for better counseling regarding prognosis. Based on the confirmed top deregulated miRNAs in paclitaxel-resistant ovarian carcinoma, we further analyzed the associations of different miRNAs expression and survival outcomes after stratifying the OC patients into high and low miRNAs’ levels. Our analyses showed that patients those with high miR-9 and 640 level survived better than those with low results. Moreover, deregulation of miR-155, 320a, 22 and 129-5p were found to be associated with shorter PFS of the patients, although not significantly. Thus, our findings suggest that a miRNA profile may help us to distinguish patients who will respond to paclitaxel treatment and provide biomarker of poor prognosis in OC patients. However, given the small number of patients involved in the study, these results need to be interpreted with caution.
Understanding the regulatory role of miRNA may lead to better understanding of the molecular events involved in different biological processes, and,lead to the development of diagnostic tools and a novel class of drug targets for therapeutic interventions. According to the TargetScan database, there are over 1200 predicted hsa-miR-9 targets, including some familiar oncogenes. Among them, RAB34 has been confirmed as a direct target of miR-9 in OC using western blot and dual luciferase reporter assay. As a member of RAS oncogene family, RAB34 is a guanosine triphosphatase (GTPases) that can regulate budding junction and fusion of vesicle in exocytosis and endocytosis pathway . Luo et al.  has found that miR-9 was down-regulated and can be the modulator of RAB34 in gastric carcinoma, which was concordant with our finding.
There is still work to be done for better defining the mechanisms of miRNA-associated paclitaxel resistance and its potential as a future target for therapy in OC. However, our results support the conclusions that miRNA profile allows meaningful subclassification of paclitaxel-resistant ovarian tumors and prognosis prediction. FFPE samples are convenient and feasible materials for miRNA study. In addition, we find miR-9 might be correlated with the paclitaxel-sensitivity through targeting RAB34. Hopefully, these findings can ultimately be used to improve ovarian cancer patient outcome.
This work was funded by the project of Zhejiang Provincial Natural Science Foundation of China (Grant No.Y207054), National Natural Science Foundation of China (Grant No.81001164), the Fundamental Research Funds for the Central Universities (2010), and National High Technology Research and Development Program (863) (2012AA02A507).
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