A study of resveratrol to suppress proliferation of human bladder cancer cell line T24 and to affect expression of miR-34a

WANG Wei,LI Tan,LI Ying,LI Hui

Medical Journal of the Chinese People Armed Police Forces ›› 2012, Vol. 23 ›› Issue (12) : 1062-1064.

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PDF(590 KB)
Medical Journal of the Chinese People Armed Police Forces ›› 2012, Vol. 23 ›› Issue (12) : 1062-1064.

A study of resveratrol to suppress proliferation of human bladder cancer cell line T24 and to affect expression of miR-34a

  • WANG Wei1,LI Tan2,LI Ying1,LI Hui1
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Abstract

Objective To investigate the effects of resveratrol on proliferation of human bladder cancer cell line T24,and the role of miR-34a in its mechanism. Methods T24 cells were treated with resveratrol in different concentrations for 24 h. Cell proliferation was validated by MTT. Flow cytometry was used to analyse apoptosis. The expression of miR-34a was detect by real-time PCR. Results Resveratrol could inhibit the proliferation of T24 in a dose dependent manner, induce apoptosis and increase the expression of p53 significantly. Furthermore, the level of miR-34a in T24 cells was higher in resveratrol-treated group than that in the control group. Conclusions Resveratrol can suppress the proliferation of human bladder cancer cells, which may be attributed to inducing apoptosis, up-regulating miR-34a and p53.

Key words

resveratrol / bladder cancer / apoptosis / miR-34a / p53

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WANG Wei,LI Tan,LI Ying,LI Hui. A study of resveratrol to suppress proliferation of human bladder cancer cell line T24 and to affect expression of miR-34a[J]. Medical Journal of the Chinese People Armed Police Forces. 2012, 23(12): 1062-1064

References

[1] Bhat K L, Kosmeder J W, Pezzuto J M. Biological effects of resveratrol[J]. Antioxid Redox Signal, 2001,3(6):1041-1064.
[2] Jang M, Cai L, Udeani G O, et al. Cancer chemopreventive activity of resveratrol, a natural product derived from grapes[J]. Science, 1997; 275(5297): 218-220.
[3] He X, Wang Y, Zhu J H, et al. Resveratrol enhances the anti-tumor activity of the mTOR inhibitor rapamycin in multiple breast cancer cell lines mainly by suppressing rapamycin-induced AKT signaling[J]. Cancer Lett, 2011, 301(2):168-176.
[4] Passetti F, Ferreira C G, Costa F F. The impact of microRNAs and alternative splicing in pharmacogenomics[J]. Pharmacogenomics J, 2009, 9(1):1-13.
[5] 韩 宇,洪宝发,钟定荣,等. 联合表达人端粒酶反转录酶hTERT及VEGF 与肿瘤复发的关系[J]. 武警医学, 2008,19(2):105-108.
[6] Kaindl U, Eyberg I, Rohr-Udilova N, et al. The dietary antioxidants resveratrol and quercetin protect cells from exogenous pro-oxidative damage[J]. Food Chem Toxicol, 2008,46(4):1320-1326.
[7] Rokhlin O W,Scheinker V S,Taghiyev A F,et al. MicroRNA-34 mediates AR-dependent p53-induced apoptosis in prostate cancer [J]. Cancer Biol Ther, 2008, 7 (8):1288-1296.
[8] Welch C,Chen Y,Stallings R L.MicroRNA-34a functions as a potential tumor suppressor by inducing apoptosis in neuroblastoma cells[J]. Oncogene, 2007, 26 (34):5017-5022.
[9] Chang T C, Wentzel E A, Kent O A. Transactivation of miR-34a by p53 broadly influences gene expression and promotes apoptosis[J]. Mol Cell, 2007, 26(5):745-752.
[10] Hermeking H. p53 enters the microRNA world[J].Cancer Cell, 2007, 12(5):414-418.
[11] Hermeking H. The miR-34 family in cancer and apoptosis[J]. Cell Death Differ, 2010, 17(2):193-199.[ZK)]
(2012-05-19
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