Resveratrol and prostate cancer: Promising role for microRNAs

被引:107
作者
Dhar, Swati [1 ]
Hicks, Chindo [1 ,2 ]
Levenson, Anait S. [1 ,3 ]
机构
[1] Univ Mississippi, Med Ctr, Inst Canc, Jackson, MS 39216 USA
[2] Univ Mississippi, Med Ctr, Ctr Biostat & Bioinformat, Jackson, MS 39216 USA
[3] Univ Mississippi, Med Ctr, Dept Pathol, Jackson, MS 39216 USA
关键词
Down-regulation of oncomiRs; miRNAs; Prostate cancer; PTEN; Resveratrol; HUMAN LUNG CANCERS; CELL-CYCLE ARREST; NF-KAPPA-B; TUMOR-GROWTH; EXPRESSION PROFILE; APOPTOSIS; SUPPRESSOR; RECEPTOR; TARGETS; MIRNAS;
D O I
10.1002/mnfr.201100141
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Scope: Resveratrol (Res) has anticancer activity in prostate cancer (PCa), which can be attributed to modulation of microRNAs (miRNAs/miRs). miRNAs/miRs are small non-coding RNAs that negatively regulate gene expression. We have analyzed differential miRNA expression in PCa cells treated with Res. Methods and results: Using miRNA microarrays we found that 23 miRNAs were significantly down-regulated and 28 miRNAs were significantly up-regulated after Res treatment. The down-regulated miRs included miR-17-92 and miR-106ab clusters with well recognized oncogenic properties while the up-regulated miRs included several tumor suppressors. Selected miRs were verified by qRT-PCR, including miR-17, miR-20a, miR-20b, miR-106a and miR106b. Since these miRNAs target PTEN (phosphatase and tensin homolog deleted on chromosome 10), we performed Western blot to confirm up-regulation of PTEN in PCa cells. In addition, using TargetScan database, we have identified putative mRNA targets for Res-induced down-and up-regulated miRs. Using a bioinformatics approach, we generated gene networks specifically altered by Res-regulated miRNAs. Conclusion: Our results indicate that the dietary compound Res may play an important role in prostate carcinogenesis through modulation of miRNA expression: Res down-regulated oncogenic miRs and up-regulated tumor suppressor miRs in PCa cells. Further in-depth studies are necessary in order to fully recognize the beneficial miRNA-mediated effects of Res in PCa.
引用
收藏
页码:1219 / 1229
页数:11
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