Global analysis of the differentially expressed miRNAs of prostate cancer in Chinese patients
- Hui-chan He†1,
- Zhao-dong Han†1,
- Qi-shan Dai1,
- Xiao-hui Ling2,
- Xin Fu1,
- Zhuo-yuan Lin1,
- Ye-han Deng1,
- Guo-qiang Qin2,
- Chao Cai2,
- Jia-hong Chen1,
- Fu-neng Jiang1,
- Xingyin Liu4Email author and
- Wei-de Zhong1, 2, 3Email author
© He et al.; licensee BioMed Central Ltd. 2013
Received: 27 February 2013
Accepted: 24 October 2013
Published: 5 November 2013
Our recent study showed the global physiological function of the differentially expressed genes of prostate cancer in Chinese patients was different from that of other non-Chinese populations. microRNA are estimated to regulate the expression of greater than 60% of all protein-coding genes. To further investigate the global association between the transcript abundance of miRNAs and their target mRNAs in Chinese patients, we used microRNA microarray approach combined with bioinformatics and clinical-pathological assay to investigate the miRNA profile and evaluate the potential of miRNAs as diagnostic and prognostic markers in Chinese patients.
A total of 28 miRNAs (fold change ≥1.5; P ≤ 0.05) were differentially expressed between tumor tissue and adjacent benign tissue of 4 prostate cancer patients.10 top Differentially expressed miRNAs were validated by qRT-PCR using all 20 tissue pairs. Compared to the miRNA profile of non-Chinese populations, the current study showed that miR-23b, miR-220, miR-221, miR-222, and miR-205 maybe common critical therapeutic targets in different populations. The integrated analysis for mRNA microarray and miRNA microarray showed the effects of specifically inhibiting and/or enhancing the function of miRNAs on the gene transcription level. The current studies also identified 15 specific expressed miRNAs in Chinese patients. The clinical feature statistics revealed that miR-374b and miR-19a have significant correlations with clinical-pathological features in Chinese patients.
Our findings showed Chinese prostate cancer patients have a common and specific miRNA expression profile compared with non-Chinese populations. The miR-374b is down-regulated in prostate cancer tissue, and it can be identified as an independent predictor of biochemical recurrence-free survival.
MicroRNAs (miRNAs) are small non-coding RNA molecules of 21-23nt that have deregulated expression in human cancer tissue . Their deregulation has been shown to play a vital role in cancer initiation, progression and metastasis  and miRNAs represent a promising new class of cancer biomarker [3, 4]. Recent studies demonstrate that miRNA expression patterns serve as phenotypic signatures of different cancers and could be used as diagnostic, prognostic and therapeutic tools . Prostate cancer is the most common cancer in men in western countries . A few studies have analyzed global microRNA expression profiles or the functional role of microRNAs in prostate cancer [7, 8]. However the results showed highly inconsistent .
Prostate cancer occurrence in the Chinese populations was lower than that of the western countries. Our recent study showed the global physiological function of the differentially expressed genes of prostate cancer in Chinese patients was different from that of other non-Chinese populations , which suggest that the deregulation of cell cycle progression maybe a “key” to differentiate the epidemiological differences between Chinese and non-Chinese. On the one hand, miRNAs are estimated to regulate the expression of greater than 60% of all protein-coding genes . On the other hand, accumulating evidence suggests that miRNAs can contribute to tumorigenesis either by directly modulating oncogenic or tumor suppressor pathways . So it should be kept in mind that there are genetic characteristics of prostate cancer patients from different populations. In the last few years, increasing evidence has documented the role of microRNAs as new broad-spectrum oncogenes or tumor suppressor genes, thus their use as diagnostic, prognostic and therapeutic biomolecules is envisaged . So more investigation on the expression profiles of miRNAs is needed to understand of the role of miRNAs in the development and progression of prostate cancer in different populations.
Recent studies have shown that microRNA inhibitory activity can be quantified by examining their target mRNA expression levels . Therefore, in order to functionally investigated differentially expressed miRNAs targets, all of patients samples in this study are same as previous report about mRNA transcript study . The objective of this study was to evaluate the potential of miRNAs as diagnostic and/or prognostic markers and to further provide a solid data basis for further functional analyses of prostate cancer-relevant miRNAs in Chinese patients.
Patients and sample collection
Prostate tissues were obtained from the tissue bank at Guangzhou Medical University. All patients who participated in the study had given informed consent. The collection of the tissue specimens in accordance with the protocol was approved by the Institutional Ethical Board of Guangzhou Medical University. The clinic pathological data of these patients are summarized in Additional file 1: Table S1. The frozen tissues were procured immediately after surgery, cut into the size of ~1 cm2 × 0.5 cm pieces, fast-frozen in liquid nitrogen and stored at -80°C.
Sample LCM and RNA preparation
The whole sample treatment and RNA extraction process were previously described by Chen JH et al. .
miRNA expression microarray
Microarray experiments were carried out using 1-color hybridizations on human miRNA Microarray (V3, 8x15K) (Agilent, Cat No.:G4471A-021827), One glass slide formatted with eight high-definition 15 K arrays, based on Sanger miRbase (release 12.0), Probes: 866 human and 89 human viral miRNAs represented. The miRNA expressions data are available at GEO (http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE34932), which included a total of 16 samples data.
Microarray data analysis
The microarray image information was converted into spot intensity values using Scanner Control Software Rev. 7.0 (Agilent). The signal after background subtraction was exported directly into the GeneSpring GX11 software (Agilent) for normalization. The mean normalized signal from biological replicates was used for comparative expression analysis. Paired t-test with Benjamini-Hochberg correction (P value ≤ 0.05) was used to identify differentially expressed miRNAs between tumor and benign tissues. The fold changes of expression signals between tumor and benign samples were calculated from the normalized values. Hierarchical clustering was performed with Pearson correlation using the differentially expressed miRNAs. 4 pairs cancer and benign tissues data (C2,C3,C4,C5,N2,N3,N4,N5) were used for further analysis.
Confirmation of miRNA expression
For miRNA detection, qRT-PCR was processing as the protocol of All-in-One™ miRNA qRT-PCR Detection Kit (Cat No.:AOMD-Q020, GeneCopoeia, China) described. All assays were carried out in triplicate. miRNA expression in each sample was normalized with the house keeping gene (RNU6B and hsa-miR-130b) expression. The specificity of amplification was confirmed by melting curve analysis and also by running PCR products on agarose gels (3%). Relative quantification of target miRNA expression was evaluated using the comparative cycle threshold (CT) method.
MiRCURY LNA™ Detection probes 5′-DIG labeled (Cat No.:18091–01 for miR-19a, 38748–01 for miR-374b, 99002-01 for U6, Exiqon, Denmark) were used to detect the in situ hybridization signal for target miRNA on formalin-fixed or frozen section of prostate tissues. In situ hybridization was performed according to the manufacturer’s instructions of Enhanced sensitivity of in situ hybridization detection kit (peroxidase) (Cat No.: MK1030, Boster, China). The result scoring of in situ hybridization experiment was detail described by He HC et al. .
Target gene prediction and integrated analysis by IPA
The selected miRNAs were further analyzed to identify the networks and pathways targets. Target prediction using TargetScan, combined with bioinformatics analysis (Ingenuity Pathway Analysis, IPA). The identified targets were compared with mRNA microarray (GEO Accession No: GSE28204) from the same patients to evaluate the implications of the altered miRNA expression .
Data comparing differences in levels of expression of miRNAs between tumor tissue and adjacent benign tissue were analyzed using paired Student’s t-test by the software of Genespring version GX 11 (Agilent Inc, USA). Other data were statistically analyzed by the software of SPSS version13.0 for Windows (SPSS Inc, USA). Continuous variables were expressed as , paired Student’s t-test for qRT-PCR data, independent t-test for in situ hybridization result, Kaplan-Meier method for biochemical recurrence free-survival, and Cox regression model for the univariate and multivariate analysis. Differences were considered statistically significant when P < 0.05.
miRNA expression profiling of clinical samples
The differentially expressed miRNAs in PCa (Fold change ≥ 1.5, P < 0.05)
miRNA microarray data
Validation of differentially expressed miRNA by qRT-PCR analysis
Functional analysis of differentially expressed miRNA by global and integrated analysis of the miRNA and mRNA expression profile
Common and specific features of miRNA expression profile in PCa tissues from Chinese patients
On the basis of these microarray experiments, we compared our data with other microarray data regarding Western PCa patients (Additional file 5: Table S5, GEO accession numbers for Taylor data, Schaefer data, and Lin data are GSE21036, GSE14857, and GSE36802, respectively). 13 differentially expressed miRNAs of our microarray data—miR-23b, miR-30c, miR-221, miR-221-5p, miR-222, miR-224, miR-205, miR-455-3p, miR-505, miR-663, miR-1224-5p, miR-1225-5p and hcmv-miR-UL70-3p—showed the same expression pattern as that of Western patients (Additional file 5: Table S5). Among these miRNAs, miR-205 was the most down-regulated miRNA both in our data and other 3 GEO data. Thus, our data reflect the shared feature of the miRNA expression profile in PCa tissues. Nevertheless, after conducting an additional literature search(Additional file 5: Table S5), we identified 15 differentially expressed miRNAs (miR-19a, miR-26b, miR-155, miR-181d, miR-188-5p, miR-193a-5p, miR-200b-5p, miR-335, miR-374a, miR-374b, miR-574-5p, miR-939, miR-1249, miR-1915, kshv-miR-K123) that have not been reported in Western PCa patients. Given the confirmed result of the qRT-PCR, miR-188-5p, miR-19a, miR-193a-5p, and miR-374b were chosen to further study the association of miRNA expression with the clinical-pathological features of PCa patients.
Association of miRNA expression with the clinic-pathological features of PCa patients
4.87 ± 0.62
3.81 ± 1.19
4.75 ± 0.97
4.08 ± 1.05
Serum PSA levels (ng/ml) #
4.80 ± 0.66
4.00 ± 0.81
5.16 ± 0.44
4.00 ± 1.17
Gleason score #
4.91 ± 0.44
3.01 ± 1.571
4.68 ± 1.11
4.28 ± 0.692
Clinical stage #
4.76 ± 0.65
3.94 ± 0.146
4.96 ± 0.55
4.21 ± 0.856
Pathological stage #
4.82 ± 0.52
3.64 ± 1.480
4.91 ± 0.80
4.21 ± 0.775
4.89 ± 0.49
4.25 ± 0.076
4.57 ± 1.50
2.70 ± 1.661
4.91 ± 0.55
4.13 ± 0.096
4.04 ± 1.66
2.65 ± 1.655
PSA failure #
4.88 ± 0.45
4.31 ± 0.081
4.86 ± 0.90
3.36 ± 1.419
Prognostic value of miRNA expression for the biochemical recurrence-free survival in univariate and multivariate analyses by Cox regression
Hazard ratio(95% CI)
Pathological tumor stage
Clinical stage group
Pathological tumor stage
In this study,we elaborated on the miRNA expression profile by using microarray in 4 matched pairs of histologically confirmed tumor tissue and adjacent benign tissue. Remarkably, 28 of the miRNAs showed differential expression. Some miRNAs were subsequently validated by qRT-PCR analyses of 20 tissue pairs. Some of the miRNAs were of special interest because of their putative targets. Because putative target genes for differentially expressed miRNAs are a first step in understanding miRNAs with potential significance in the process of tumor development, we identified putative target genes for each of the differentially expressed miRNAs using IPA software. To provide a foundation for our functional analyses, we performed an integrated analysis for our previous mRNA microarray database and IPA-predicted miRNA target analysis (Additional file 2: Table S2). miR-205 has been reported to be down-regulated in prostate cancer patients and has been shown to be oncogenic [14–17]. Recently, Gandellini et al.  reported that miR-205 is essential for maintenance of the base membrane (BM) in prostate epithelium and pointed out that miR-205 may favour tumorigenesis by creating discontinuities in the BM. Actually, the network analysis showed centre localization of miR-205 (Figure 3), and IPA analysis for predicting targets of miR-205 showed that these targets play a role in regulating tumor morphology, which suggests that miR-205 maybe involved in prostate cancer progression. E2F1 as miR-205 target was observed in this network, interestingly, E2F1 is one of the most frequently observed potential markers for discriminating benign and malignant disease . When comparing these targets shown in the network to our previous mRNA microarray data , however, we found that only TLK targeted by miR-205 showed significant up-regulation. Ronald et al.  reported that TLK expressed in a panel of PCa cell lines and their related to radioresistance. Furthermore, the expression of TLK1B in non-expressing PC-3 cells rendered them highly resistant to radiation; conversely, a knockdown to TLK1/1B in expressing DU145 reduced their radio tolerance. TLKs appear to be intimately linked to the pattern of resistance to DNA damage, and specifically to double-strand break(DSB) repair. Hence, our microarray data confirms the possibility of extending the downstream signaling of miR-205 involved in the DNA repair process.
Down-regulation of miR-221 and miR-222 has also been frequently observed in prostate cancer samples [8, 20, 21]. Our analysis is in concordance with these prior studies of prostate cancer. IPA analysis for targets of miR-221/222 showed that these targets play a role in regulating tumor morphology. Interestingly, some of the differentially expressed genes targeted by miR-221 and miR-222 have previously been associated with prostate cancer in Western patients, such as Ttspan13, which is overexpressed in prostate cancer and whose expression correlates with factors of favourable outcomes . Among the candidates, CDON encodes the CDO protein, an orphan cell surface receptor from the immunoglobulin superfamily. Additional quantitative RT-PCR revealed that 83% of PCa tissues showed CDON overexpression. Knockdown of CDON in DU145 cells induced 5-fluorouracil-induced apoptosis and inhibited invasion ability. Therefore, CDON was suggested, as it has a high potential as a therapeutic target for PCa .
A down-regulated expression level of miR-23b was found in malignant tissues of prostate cancer . Ectopic expression of these miRNAs significantly reduced LNCaP cancer cell growth, suggesting growth-modulatory roles for miR-23b. Majidand and his colleagues  reported that miR-23b expression caused a dramatic decrease in tumor growth in nude mice and attenuated Src expression. Also, the increased expression of miR-23b inhibited proliferation, colony formation, and migration/invasion and triggered G0/G1 cell cycle arrest and apoptosis in PCa . As such, these findings suggest that re-expression of miR-23b may contribute to the epigenetic therapy for PCa. In our recent study , we also identified miR-23b as a candidate miRNA that targets PRDX3. The expression levels of miR-23b and PRDX3 in PCa tissues were found to be related to the severity of the tumor malignancy, suggesting their clinical relevance. The integrated miRNA target analysis showed that most of the targets for miR-23b are known to be involved in cellular assembly and the cell cycle. Based on the above information, we speculate that the activity of miR-23b may be conserved in Western and Chinese patients. Our integrated mRNA and miRNA analysis extends the downstream signaling of their studies and provides more comprehensive information about miR-23b in tumor growth.
In a number of studies, miRNAs such as let-7 family , miR-148 [26, 27], and miR-210 [28, 29] were also found to be up-regulated in prostate cancer, and miR-31  and miR-145b [20, 21, 31] and miR-126  were found to be down-regulated; in our study of Chinese patients, however, these miRNAs showed no significant change. The reason for these discrepancies is not clear. Recently, BoydLk et al.  pointed out that prostate cancer is a genetic disease characterized by multiple genomic alterations, including point mutations, microsatellite variations, and chromosomal alterations such as translocations, insertions, duplications, and deletions. The study suggests that the potential effects of the complex nature and heterogeneity of this disease might lead to miRNAs’ being differentially expressed in different populations.
Among the identified 15 differentially expressed miRNAs in Chinese patients, we selected miR-188-5p, miR-19a, miR-193a-5p, and miR-374b for further study and found that only miR-374b and miR-19a showed the association of miRNA expression with the clinical-pathological features of PCA patients.
IPA pathway analysis showed that the targets of the two miRNAs also had a critical role in cellular assembly and organization, DNA replication, recombination and repair cellular compromise, and the cell cycle. It is of interest that many of the target genes associated with the differentially expressed mRNAs in prostate cancer were found to be identical to the predicted target genes of differentially expressed miRNAs, as well as to be related to cancer and metastasis—e.g. TOP1 , RALA , SNX18, PNPT1 , PARD6B , KRAS  and HIPK2 .
Additionally, Up-regulated expression of miR-19a was found in lung cancer and colorectal cancer [39–42]. Our current study firstly reported miR-19a up-regulated in PCa with clinical-pathological features in Chinese patients but not in non-Chinese patients. The result provides a starting point for future research into the function of miR-19a and suggests that miR-19a up-regulated may involve heterogeneous disorder of Chinese patients.
MiR-374b was reported as being involved in multiple physical functions and diseases, such as adipocyte differentiation [43, 44], lipid metabolism, renal Ca2+ homeostasis , vascular permeability in injury , and lung cancer . Our results showed that miR-374b is an independent predictor of shorter biochemical recurrence-free survival of PCa by in situ hybridization. Interestingly, it was recently reported that miR-374 in seminal plasma can, as a diagnostic biomarker for male infertility, combine with other miRNAs . As such, our findings suggest that the further study of the miR-374b expression level in prostate fluid or serum of prostate cancer patients may promote the clinical application of the miR-374b as PCa biomarker.
Our study supports the concept that alternations of miRNA expression play an important role in prostate carcinogenesis. miR-23b, miR-220, miR-221, miR-222 and miR-205 maybe common critical therapeutic targets in the different populations. However, while a miRNA potentially has hundreds of target genes, relatively few targets have been experimentally validated. Our integrated analysis for mRNA microarray and miRNA microarray will help us to investigate the effect of specifically inhibiting/enhancing the function of miRNAs on the activity of their putative target genes, gene translation and the various stages of cancer development. This study also identifies those 15 specific expressed miRNAs in Chinese patients. The clinical feature statistics reveal that only miR-374b and miR-19a have significant correlation with clinic-pathological features, which suggest miR-374b and miR-19a may be involved in prostate cancer progression of Chinese patients.
This work was supported by grants from the National Natural Science Foundation of China (30872960, 81170699, 81272813, 81200550), the Guangzhou Municipal Science and Technology Key Project (11C23150711), the Key Projects of Bureau of Health in Guangzhou Municipality (201102A212015), and the Projects of Guangdong Key Laboratory of Urology (2010A060801016).
- Lu J, Getz G, Miska EA, Alvarez-Saavedra E, Lamb J, Peck D, Sweet-Cordero A, Ebert BL, Mak RH, Ferrando AA, Downing JR, Jacks T, Horvitz HR: GolubTR. MicroRNA expression profiles classify human cancers. Nature. 2005, 435: 834-838. 10.1038/nature03702.View ArticlePubMedGoogle Scholar
- Baranwal S, Alahari SK: miRNA control of tumor cell invasion and metastasis. Int J Cancer. 2010, 126: 1283-1290.PubMed CentralPubMedGoogle Scholar
- Gandellini P, Profumo V, Folini M, Zaffaroni N: MicroRNAs as new therapeutic targets and tools in cancer. Expert OpinTher Targets. 2011, 15: 265-279. 10.1517/14728222.2011.550878.View ArticleGoogle Scholar
- Casanova-Salas I, Rubio-Briones J, Fernández-Serra A, López-Guerrero JA: miRNAs as biomarkers in prostate cancer. ClinTransl Oncol. 2012, 14: 803-811.Google Scholar
- Saini S, Majid S, Dahiya R: Diet, microRNAs and prostate cancer. Pharm Res. 2010, 27: 1014-1026. 10.1007/s11095-010-0086-x.PubMed CentralView ArticlePubMedGoogle Scholar
- Siegel R, Naishadham D, Jemal A: Cancer statistics, 2012. CA Cancer J Clin. 2012, 62: 10-29. 10.3322/caac.20138.View ArticlePubMedGoogle Scholar
- Szczyrba J, Löprich E, Wach S, Jung V, Unteregger G, Barth S, Grobholz R, Wieland W, Stöhr R, Hartmann A, Wullich B, Grässer F: The microRNA profile of prostate carcinoma obtained by deep sequencing. Mol Cancer Res. 2010, 8: 529-538. 10.1158/1541-7786.MCR-09-0443.View ArticlePubMedGoogle Scholar
- Schaefer A, Jung M, Mollenkopf HJ, Wagner I, Stephan C, Jentzmik F, Miller K, Lein M, Kristiansen G, Jung K: Diagnostic and prognostic implications of microRNA profiling in prostate carcinoma. Int J Cancer. 2010, 126: 1166-1176.PubMedGoogle Scholar
- Chen JH, He HC, Jiang FN, Militar J, Ran PY, Qin GQ, Cai C, Chen XB, Zhao J, Mo ZY, Chen YR, Zhu JG, Liu X, Zhong WD: Analysis of the specific pathways and networks of prostate cancer for gene expression profiles in the Chinese population. Med Oncol. 2012, 29: 1972-1984. 10.1007/s12032-011-0088-5.View ArticlePubMedGoogle Scholar
- Davis BN, Hata A: Regulation of MicroRNA Biogenesis: a miRiad of mechanisms. Cell Commun Signal. 2009, 7: 18-10.1186/1478-811X-7-18.PubMed CentralView ArticlePubMedGoogle Scholar
- Negrini M, Nicoloso MS, Calin GA: MicroRNAs and cancer–new paradigms in molecular oncology. Curr Opin Cell Biol. 2009, 21: 470-479. 10.1016/j.ceb.2009.03.002.View ArticlePubMedGoogle Scholar
- Fu X, Xue C, Huang Y, Xie Y, Li Y: The activity and expression of microRNAs in prostate cancers. Mol Biosyst. 2010, 6: 2561-2572. 10.1039/c0mb00100g.View ArticlePubMedGoogle Scholar
- He HC, Zhu JG, Chen XB, Chen SM, Han ZD, Dai QS, Ling XH, Fu X, Lin ZY, Deng YH, Qin GQ, Cai C, Chen JH, Zhong WD: MicroRNA-23b downregulatesperoxiredoxin III in human prostate cancer. FEBS Lett. 2012, 586: 2451-2458. 10.1016/j.febslet.2012.06.003.View ArticlePubMedGoogle Scholar
- Gandellini P, Folini M, Longoni N, Pennati M, Binda M, Colecchia M, Salvioni R, Supino R, Moretti R, Limonta P, Valdagni R, Daidone MG, Zaffaroni N: miR-205 exerts tumor-suppressive functions in human prostate through down-regulation of protein kinase Cepsilon. Cancer Res. 2009, 69: 2287-2295. 10.1158/0008-5472.CAN-08-2894.View ArticlePubMedGoogle Scholar
- Majid S, Dar AA, Saini S, Yamamura S, Hirata H, Tanaka Y, Deng G, Dahiya R: MicroRNA-205-directed transcriptional activation of tumor suppressor genes in prostate cancer. Cancer. 2010, 116: 5637-5649. 10.1002/cncr.25488.PubMed CentralView ArticlePubMedGoogle Scholar
- Boll K, Reiche K, Kasack K, Mörbt N, Kretzschmar AK, Tomm JM, Verhaegh G, Schalken J, von Bergen M, Horn F, Hackermüller J: MiR-130a, miR-203 and miR-205 jointly repress key oncogenic pathways and are downregulated in prostate carcinoma. Oncogene. 2013, 32: 277-285. 10.1038/onc.2012.55.View ArticlePubMedGoogle Scholar
- Gandellini P, Profumo V, Casamichele A, Fenderico N, Borrelli S, Petrovich G, Santilli G, Callari M, Colecchia M, Pozzi S, De Cesare M, Folini M, Valdagni R, Mantovani R, Zaffaroni N: miR-205 regulates basement membrane deposition in human prostate: implications for cancer development. Cell Death Differ. 2012, 19: 1750-1760. 10.1038/cdd.2012.56.PubMed CentralView ArticlePubMedGoogle Scholar
- Pipinikas CP, Nair SB, Kirby RS, Carter ND, Fenske CD: Measurement of blood E2F3 mRNA in prostate cancer by quantitative RT-PCR: a preliminary study. Biomarkers. 2007, 12: 541-557. 10.1080/13547500701391353.View ArticlePubMedGoogle Scholar
- Ronald S, Sunavala-Dossabhoy G, Adams L, Williams B, De Benedetti A: The expression of tousled kinases in CaP cell lines and its relation to radiation response and DSB repair. Prostate. 2011, 71: 1367-1373. 10.1002/pros.21358.View ArticlePubMedGoogle Scholar
- Porkka KP, Pfeiffer MJ, Waltering KK, Vessella RL, Tammela TL, Visakorpi T: MicroRNA expression profiling in prostate cancer. Cancer Res. 2007, 67: 6130-6135. 10.1158/0008-5472.CAN-07-0533.View ArticlePubMedGoogle Scholar
- Tong AW, Fulgham P, Jay C, Chen P, Khalil I, Liu S, Senzer N, Eklund AC, Han J, Nemunaitis J: MicroRNA profile analysis of human prostate cancers. Cancer Gene Ther. 2009, 16: 206-216.PubMedGoogle Scholar
- Arencibia JM, Martín S, Pérez-Rodríguez FJ, Bonnin A: Gene expression profiling reveals overexpression of TSPAN13 in prostate cancer. Int J Oncol. 2009, 34: 457-463.PubMedGoogle Scholar
- Hayashi T, Oue N, Sakamoto N, Anami K, Oo HZ, Sentani K, Ohara S, Teishima J, Matsubara A, Yasui W: Identification of transmembrane protein in prostate cancer by the Escherichia coli ampicillin secretion trap: expression of CDON is involved in tumor cell growth and invasion. Pathobiology. 2011, 78: 277-284. 10.1159/000329588.View ArticlePubMedGoogle Scholar
- Majid S, Dar AA, Saini S, Arora S, Shahryari V, Zaman MS, Chang I, Yamamura S, Tanaka Y, Deng G, Dahiya R: MicroRNA-23b represses proto-oncogene Src kinase, functions as a methylation-silenced tumor suppressor with diagnostic and prognostic significance in prostate cancer. Cancer Res. 2012, 72: 6435-6446. 10.1158/0008-5472.CAN-12-2181.PubMed CentralView ArticlePubMedGoogle Scholar
- Jiang J, Lee EJ, Gusev Y, Schmittgen TD: Real-time expression profiling of microRNA precursors in human cancer cell lines. Nucleic Acids Res. 2005, 33: 5394-5403. 10.1093/nar/gki863.PubMed CentralView ArticlePubMedGoogle Scholar
- Fujita Y, Kojima K, Ohhashi R, Hamada N, Nozawa Y, Kitamoto A, Sato A, Kondo S, Kojima T, Deguchi T, Ito M: MiR-148a attenuates paclitaxel resistance of hormone-refractory, drug-resistant prostate cancer PC3 cells by regulating MSK1 expression. J Biol Chem. 2010, 285: 19076-19084. 10.1074/jbc.M109.079525.PubMed CentralView ArticlePubMedGoogle Scholar
- Murata T, Takayama K, Katayama S, Urano T, Horie-Inoue K, Ikeda K, Takahashi S, Kawazu C, Hasegawa A, Ouchi Y, Homma Y, Hayashizaki Y, Inoue S: miR-148a is an androgen-responsive microRNA that promotes LNCaP prostate cell growth by repressing its target CAND1 expression. Prostate Cancer Prostatic Dis. 2010, 13: 356-361. 10.1038/pcan.2010.32.View ArticlePubMedGoogle Scholar
- Quero L, Dubois L, Lieuwes NG, Hennequin C, Lambin P: miR-210 as a marker of chronic hypoxia, but not a therapeutic target in prostate cancer. Radiother Oncol. 2011, 101: 203-208. 10.1016/j.radonc.2011.05.063.View ArticlePubMedGoogle Scholar
- Roa W, Brunet B, Guo L, Amanie J, Fairchild A, Gabos Z, Nijjar T, Scrimger R, Yee D, Xing J: Identification of a new microRNA expression profile as a potential cancer screening tool. Clin Invest Med. 2010, 33: E124-PubMedGoogle Scholar
- Creighton CJ, Fountain MD, Yu Z, Nagaraja AK, Zhu H, Khan M, Olokpa E, Zariff A, Gunaratne PH, Matzuk MM, Anderson ML: Molecular profiling uncovers a p53-associated role for microRNA-31 in inhibiting the proliferation of serous ovarian carcinomas and other cancers. Cancer Res. 2010, 70: 1906-1915. 10.1158/0008-5472.CAN-09-3875.PubMed CentralView ArticlePubMedGoogle Scholar
- Prueitt RL, Yi M, Hudson RS, Wallace TA, Howe TM, Yfantis HG, Lee DH, Stephens RM, Liu CG, Calin GA, Croce CM, Ambs S: Expression of microRNAs and protein-coding genes associated with perineural invasion in prostate cancer. Prostate. 2008, 68: 1152-1164. 10.1002/pros.20786.PubMed CentralView ArticlePubMedGoogle Scholar
- Boyd LK, Mao X, Lu YJ: The complexity of prostate cancer: genomic alterations and heterogeneity. Nat Rev Urol. 2012, 9: 652-664. 10.1038/nrurol.2012.185.View ArticlePubMedGoogle Scholar
- Sereno M, Cejas P, Moreno V, Belda-Iniesta C, López R, Nistal M, Feliu J, De Castro CJ: ERCC1 and topoisomerase I expression in small cell lung cancer: prognostic and predictive implications. Int J Oncol. 2012, 40: 2104-2110.PubMedGoogle Scholar
- Peschard P, McCarthy A, Leblanc-Dominguez V, Yeo M, Guichard S, Stamp G, Marshall CJ: Genetic deletion of RALA and RALB small GTPases reveals redundant functions in development and tumorigenesis. Curr Biol. 2012, 22: 2063-2068. 10.1016/j.cub.2012.09.013.View ArticlePubMedGoogle Scholar
- Luczynski W, Kowalczuk O, Stasiak-Barmuta A, Ilendo E, Krawczuk-Rybak M, Chyczewski L: Acute lymphoblastic leukemia-derived dendritic cells express tumor associated antigens: PNPT1, PMPCB, RHAMM, BSG and ERCC1. Neoplasma. 2009, 56: 428-434. 10.4149/neo_2009_05_428.View ArticlePubMedGoogle Scholar
- Cunliffe HE, Jiang Y, Fornace KM, Yang F, Meltzer PS: PAR6B is required for tight junction formation and activated PKCæ localization in breast cancer. Am J Cancer Res. 2012, 2: 478-491.PubMed CentralPubMedGoogle Scholar
- Wang XS, Shankar S, Dhanasekaran SM, Ateeq B, Sasaki AT, Jing X, Robinson D, Cao Q, Prensner JR, Yocum AK, Wang R, Fries DF, Han B, Asangani IA, Cao X, Li Y, Omenn GS, Pflueger D, Gopalan A, Reuter VE, Kahoud ER, Cantley LC, Rubin MA, Palanisamy N, Varambally S, Chinnaiyan AM: Characterization of KRAS rearrangements in metastatic prostate cancer. Cancer Discov. 2011, 1: 35-43. 10.1158/2159-8274.CD-10-0022.PubMed CentralView ArticlePubMedGoogle Scholar
- Hofmann TG, Glas C, Bitomsky N: HIPK2: A tumour suppressor that controls DNA damage-induced cell fate and cytokinesis. Bioessays. 2013, 35: 55-64. 10.1002/bies.201200060.View ArticlePubMedGoogle Scholar
- Malzkorn B, Wolter M, Liesenberg F, Grzendowski M, Stühler K, Meyer HE, Reifenberger G: Identification and functional characterization of microRNAs involved in the malignant progression of gliomas. Brain Pathol. 2010, 20: 539-550. 10.1111/j.1750-3639.2009.00328.x.View ArticlePubMedGoogle Scholar
- Reichek JL, Duan F, Smith LM, Gustafson DM, O’Connor RS, Zhang C, Dunlevy MJ, Gastier-Foster JM, Barr FG: Genomic and clinical analysis of amplification of the 13q31 chromosomal region in alveolar rhabdomyosarcoma: a report from the children’s oncology group. Clin Cancer Res. 2011, 17: 1463-1473. 10.1158/1078-0432.CCR-10-0091.PubMed CentralView ArticlePubMedGoogle Scholar
- Uziel T, Karginov FV, Xie S, Parker JS, Wang YD, Gajjar A, He L, Ellison D, Gilbertson RJ, Hannon G, Roussel MF: The miR-17 92 cluster collaborates with the sonic hedgehog pathway in medulloblastoma. Proc Natl Acad Sci USA. 2009, 106: 2812-2817. 10.1073/pnas.0809579106.PubMed CentralView ArticlePubMedGoogle Scholar
- Zhang J, Xiao Z, Lai D, Sun J, He C, Chu Z, Ye H, Chen S, Wang J: miR-21, miR-17 and miR-19a induced by phosphatase of regenerating liver-3 promote the proliferation and metastasis of colon cancer. Br J Cancer. 2012, 107 (2): 352-359. 10.1038/bjc.2012.251.PubMed CentralView ArticlePubMedGoogle Scholar
- Pan S, Zheng Y, Zhao R, Yang X: miRNA-374 regulates dexamethasone-induced differentiation of primary cultures of porcine adipocytes. Horm Metab Res. 2013, 45: 518-525.View ArticlePubMedGoogle Scholar
- Pan S, Zheng Y, Zhao R, Yang X: MicroRNA-130b and microRNA-374b mediate the effect of maternal dietary protein on offspring lipid metabolism in Meishan pigs. Br J Nutr. 2013, 109: 1731-1738. 10.1017/S0007114512003728.View ArticlePubMedGoogle Scholar
- Gong Y, Renigunta V, Himmerkus N, Zhang J, Renigunta A, Bleich M, Hou J: Claudin-14 regulates renal Ca++ transport in response to CaSRsignalling via a novel microRNA pathway. EMBO J. 2012, 31: 1999-2012. 10.1038/emboj.2012.49.PubMed CentralView ArticlePubMedGoogle Scholar
- Adyshev DM, Moldobaeva N, Mapes B, Elangovan V, Garcia JG: MicroRNA regulation of nonmuscle myosin light chain kinase expression in human lung endothelium. Am J Respir Cell Mol Biol. 2013, 49: 58-66. 10.1165/rcmb.2012-0397OC.PubMed CentralView ArticlePubMedGoogle Scholar
- Miko E, Czimmerer Z, Csánky E, Boros G, Buslig J, Dezso B, Scholtz B: Differentially expressed microRNAs in small cell lung cancer. Exp Lung Res. 2009, 35: 646-664. 10.3109/01902140902822312.View ArticlePubMedGoogle Scholar
- Wang C, Yang C, Chen X, Yao B, Yang C, Zhu C, Li L, Wang J, Li X, Shao Y, Liu Y, Ji J, Zhang J, Zen K, Zhang CY, Zhang C: Altered profile of seminal plasma microRNAs in the molecular diagnosis of male infertility. Clin Chem. 2011, 57: 1722-1731. 10.1373/clinchem.2011.169714.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.