Ha Yun-Hyung, Park Dong-Guk
Department of Surgery, Dankook University School of Medicine, Cheonan, Korea.
J Korean Soc Coloproctol. 2010 Aug;26(4):254-9. doi: 10.3393/jksc.2010.26.4.254. Epub 2010 Aug 31.
Evidence that indicates bile acid is a promoter of colon cancer exists. Deoxycholic acid (DCA) modifies apoptosis or proliferation by affecting intracellular signaling and gene expression. However, because previous studies have been based on studies on colon cancer cell lines, the effect of DCA on normal colonocytes is unknown.
Normal colonocytes and Caco-2 and HCT116 cells were treated with 20 µM and 250 µM of DCA, and the effect of different concentrations of DCA was measured based on the expression of cell-cycle-related proteins by using Western blots.
The expressions of CDK2 and cyclin D1 for different concentrations of DCA in normal colonocytes and colon cancer cells were similar, but the expressions of cyclin E and A were significantly different. In HCT116 colon cancer cells, the expression of cyclin E increased regardless of the DCA concentration, but in normal colonocytes and Caco-2 cells, the expression of cyclin E was not changed or decreased. In HCT116 colon cancer cells, the expression of cyclin A was not changed or decreased regardless of the DCA concentration, but in normal colonocytes and Caco-2 cells, the expression of cyclin A was increased at a DCA concentration of 20 µM.
The effect of DCA on stimulating cell proliferation suggests that DNA synthesis is stimulated by an increased expression of cyclin E in colon cancer cells. Our results suggest that a low dose of DCA induces cellular proliferation through increased expression of cyclin A and that a high dose of DCA induces decreased expression of cyclin E and CDK2 in normal colonocytes.
有证据表明胆汁酸是结肠癌的促发因素。脱氧胆酸(DCA)通过影响细胞内信号传导和基因表达来改变细胞凋亡或增殖。然而,由于先前的研究基于结肠癌细胞系,DCA对正常结肠细胞的影响尚不清楚。
用20μM和250μM的DCA处理正常结肠细胞、Caco-2细胞和HCT116细胞,并通过蛋白质免疫印迹法基于细胞周期相关蛋白的表达来测定不同浓度DCA的作用。
不同浓度DCA作用下,正常结肠细胞和结肠癌细胞中CDK2和细胞周期蛋白D1的表达相似,但细胞周期蛋白E和A的表达存在显著差异。在HCT116结肠癌细胞中,无论DCA浓度如何,细胞周期蛋白E的表达均增加,但在正常结肠细胞和Caco-2细胞中,细胞周期蛋白E的表达未发生变化或降低。在HCT116结肠癌细胞中,无论DCA浓度如何,细胞周期蛋白A的表达未发生变化或降低,但在正常结肠细胞和Caco-2细胞中,20μM DCA浓度时细胞周期蛋白A的表达增加。
DCA对刺激细胞增殖的作用表明,细胞周期蛋白E表达增加刺激了结肠癌细胞中的DNA合成。我们的结果表明,低剂量DCA通过增加细胞周期蛋白A的表达诱导细胞增殖,而高剂量DCA诱导正常结肠细胞中细胞周期蛋白E和CDK2的表达降低。