Gastric Cancer
Copyright ©The Author(s) 2002. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Oct 15, 2002; 8(5): 782-786
Published online Oct 15, 2002. doi: 10.3748/wjg.v8.i5.782
The effects of vitamin E succinate on the expression of c-jun gene and protein in human gastric cancer SGC-7901 cells
Yan Zhao, Kun Wu, Wei Xia, Yu-Juan Shan, Li-Jie Wu, Wei-Ping Yu
Yan Zhao, Kun Wu, Wei Xia, Yu-Juan Shan, Li-Jie Wu, Department of Nutrition and Food Hygiene, Public Health School, Harbin Medical University, Harbin 150001, Heilongjiang Province, China
Wei-Ping Yu, Genetics Institute, Texas University of USA, Austin, USA
Author contributions: All authors contributed equally to the work.
Supported by National Natural Science Foundation of China, No.39870662
Correspondence to: Prof. Kun Wu, Department of Nutrition and Food Hygiene, Public Health School, Harbin Medical University, Harbin 150001, Heilongjiang Province, China. wukun@public.hr.hl.cn
Telephone: +86-451-3648665
Received: March 11, 2002
Revised: April 12, 2002
Accepted: April 20, 2002
Published online: October 15, 2002
Abstract

AIM: To investigate the effects of vitamin E succinate (VES) on the expression of c-jun gene and protein in human gastric cancer SGC-7901 cells.

METHODS: After SGC-7901 cells were treated with VES at different doses (5, 10, 20 mg•L-1) at different time, reverse transcription-PCR technique was used to detect the level of c-jun mRNA; Western Blot was applied to measure the expression of c-jun protein.

RESULTS: After the cells were treated with VES at 20 mg•L-1 for 3 h, the expression rapidly reached its maximum that was 3.5 times of UT control (P < 0.01). The level of c-jun mRNA was also increased following treatment of VES for 6 h. However, the expression after treatment of VES at 5 mg•L-1 for 24 h was 1.6 times compared with UT control (P < 0.01). Western blot analysis showed that the level of c-jun protein was obviously elevated in VES-treated SGC-7901 cells at 20 mg•L-1 for 3 h. The expression of c-jun protein was gradually increased after treatment of VES at 20 mg•L-1 for 3, 6, 12 and 24 h, respectively, with an evident time-effect relationship.

CONCLUSION: The levels of c-jun mRNA and protein in VES-treated SGC-7901 cells were increased in a dose- and time-dependent manner; the expression of c-jun was prolonged by VES, indicating that c-jun is involved in VES-induced apoptosis in SGC-7901 cells.

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