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Effect of bFGF on cyclin D1 and GADD153 expression in human ovarian cancer CAOV3 cells
Authors:YE Li-ping  WEN You-feng  NIE Hai-qi  ZHANG Ying
Affiliation:1.Department of Pathophysiology, 2Department of Anatomy, Liaoning Medical College, Jinzhou 121001, China;3.The Blood Center of Liaoning Province, Shenyang 110044, China;4.Department of Biochemistry and Molecular Biology, China Medical University, Shenyang 110001, China.E-mail:ye960519@126.com
Abstract:AIM: To evaluate the effect of basic fibroblast growth factor (bFGF) on the expression of cyclin D1, growth arrest, DNA damage inducible gene 153 (GADD153), and its roles involved in cell cycle regulation and DNA repair in starvation-induced ovarian cancer CAOV3 cells apoptosis. METHODS: Apoptosis of ovarian cancer CAOV3 cells was induced by serum-free culture (starvation). After bFGF treatment, the cell proliferation rate, cell cycle and apoptosis were determined by MTT, FACS analysis and agarose electrophoresis, respectively. The expression of c-Fos, c-Jun and cyclin D1, GADD153 were detected by Western blotting. RESULTS: bFGF increased the cell proliferation and prevented starvation-induced cell apoptosis. In a time-dependent manner, bFGF induced the expression of c-Fos, c-Jun and cyclin D1 and inhibited GADD153. CONCLUSION: bFGF plays a critical role in anti-apoptosis and the proliferation in human ovarian cancer by upregulating the expression of c-Fos, c-Jun and cyclin D1 and inhibiting GADD153.
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