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Therapeutic Potential of an Anti-diabetic Drug, Metformin: Alteration of miRNA expression in Prostate Cancer Cells

Authors :
Cigir Biray Avci
Sunde Yilmaz Susluer
Yavuz Dodurga
Cumhur Gündüz
Ece Harman
Ege Üniversitesi
Source :
Asian Pacific Journal of Cancer Prevention. 14:765-768
Publication Year :
2013
Publisher :
Asian Pacific Organization for Cancer Prevention, 2013.

Abstract

WOS: 000324920000028<br />PubMed ID: 23621234<br />Background and Aims: Prostate cancer is the most commonly diagnosed cancer in males in many populations. Metformin is the most widely used anti-diabetic drug in the world, and there is increasing evidence of a potential efficacy of this agent as an anti-cancer drug. Metformin inhibits the proliferation of a range of cancer cells including prostate, colon, breast, ovarian, and glioma lines. MicroRNAs (miRNAs) are a class of small, non-coding, single-stranded RNAs that downregulate gene expression. We aimed to evaluate the effects of metformin treatment on changes in miRNA expression in PC-3 cells, and possible associations with biological behaviour. Materials and Methods: Average cell viability and cytotoxic effects of metformin were investigated at 24 hour intervals for three days using the xCELLigence system. The IC50 dose of metformin in the PC-3 cells was found to be 5 mM. RNA samples were used for analysis using custom multi-species microarrays containing 1209 probes covering 1221 human mature microRNAs present in miRBase 16.0 database. Results: Among the human miRNAs investigated by the arrays, 10 miRNAs were up-regulated and 12 miRNAs were down-regulated in the metformin-treated group as compared to the control group. In conclusion, expression changes in miRNAs of miR-146a, miR-100, miR-425, miR-193a-3p and, miR-106b in metformin-treated cells may be important. This study may emphasize a new role of metformin on the regulation of miRNAs in prostate cancer.

Details

ISSN :
15137368 and 00032492
Volume :
14
Database :
OpenAIRE
Journal :
Asian Pacific Journal of Cancer Prevention
Accession number :
edsair.doi.dedup.....c00c1805ea6178d7a81255fda1cb81b5
Full Text :
https://doi.org/10.7314/apjcp.2013.14.2.765