Effects of DCA on Cell Cycle Proteins in Colonocytes.
10.3393/jksc.2010.26.4.254
- Author:
Yun Hyung HA
1
;
Dong Guk PARK
Author Information
1. Department of Surgery, Dankook University School of Medicine, Cheonan, Korea. dkpark@dankook.ac.kr
- Publication Type:Original Article
- Keywords:
Deoxycholic acid;
Cell cycle;
Cyclin;
Colonocyte;
CDK2
- MeSH:
Apoptosis;
Bile;
Blotting, Western;
Caco-2 Cells;
Cell Cycle;
Cell Cycle Proteins;
Cell Line;
Cell Proliferation;
Colonic Neoplasms;
Cyclin A;
Cyclin D1;
Cyclin E;
Cyclins;
Deoxycholic Acid;
DNA;
Gene Expression;
HCT116 Cells;
Humans;
Proteins
- From:Journal of the Korean Society of Coloproctology
2010;26(4):254-259
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: 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. METHODS: Normal colonocytes and Caco-2 and HCT116 cells were treated with 20 micrometer and 250 micrometer 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. RESULTS: 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 micrometer. CONCLUSION: 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.
