Zhang Yan-Lun, Wang Peng, Lu You-Yi, Hu Nai-Gang
Department of Urology, Qingdao Municipal Hospital, Qingdao, Shandong 266011, China.
Zhonghua Nan Ke Xue. 2009 Dec;15(12):1098-101.
To investigate the inhibitory effect of polypeptide K237 on the proliferation of human hormone refractory prostate cancer cell line PC-3M and its possible mechanism.
PC-3M cells were divided into three experimental groups and a control, treated with polypeptide K237 at the concentration of 50, 100, 200 and 0 micromol/L, respectively, for 48 hours. The effects of K237 on the proliferation of different groups of the PC-3M cells were analyzed by MTF, and the mRNA expression levels of bax and bcl-2 were detected by RT-PCR.
After polypeptide K237 treatment, the PC-3M cells became round, small and less transparent in cytoplasm, and some shed and suspended in the culture medium. The growth inhibition rates of the PC-3M cells were (12.6 +/- 0.95)%, (17.8 +/- 0.99)% and (27.2 +/- 1.12)% in the 50, 100 and 200 micromol/L concentration groups. RT-PCR analysis showed that the bax/beta-actin values of the 50, 100, 200 and 0 micromol/L groups were 0.919 +/- 0.071, 0.971 +/- 0.083, 0.992 +/- 0.102 and 0.889 +/- 0.067, and the bcl-2/beta-actin values of the four groups were 0.896 +/- 0.085, 0.791 +/- 0.084, 0.764 +/- 0.702 and 0.922 +/- 0.097, respectively, both with significant differences between the experimental and the control groups (P < 0.01). The mRNA expression of bax was upregulated and that of bcl-2 downregulated in a dose-dependent manner.
Polypeptide K237 may induce apoptosis of PC-3M cells by affecting the expressions of bax and bcl-2, and thus suppress the proliferation of prostate cancer cells.
探讨多肽K237对人激素难治性前列腺癌细胞系PC-3M增殖的抑制作用及其可能机制。
将PC-3M细胞分为三个实验组和一个对照组,分别用浓度为50、100、200和0微摩尔/升的多肽K237处理48小时。采用MTF分析K237对不同组PC-3M细胞增殖的影响,并用RT-PCR检测bax和bcl-2的mRNA表达水平。
经多肽K237处理后,PC-3M细胞变圆、变小,细胞质透明度降低,部分细胞脱落并悬浮于培养基中。50、100和200微摩尔/升浓度组PC-3M细胞的生长抑制率分别为(12.6±0.95)%、(17.8±0.99)%和(27.2±1.12)%。RT-PCR分析显示,50、100、200和0微摩尔/升组的bax/β-肌动蛋白值分别为0.919±0.071、0.971±0.083、0.992±0.102和0.889±0.067,四组的bcl-2/β-肌动蛋白值分别为0.896±0.085、0.791±0.084、0.764±0.702和0.922±0.097,实验组与对照组之间均有显著差异(P<0.01)。bax的mRNA表达呈剂量依赖性上调,bcl-2的mRNA表达呈剂量依赖性下调。
多肽K237可能通过影响bax和bcl-2的表达诱导PC-3M细胞凋亡,从而抑制前列腺癌细胞的增殖。