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Copyright ©2007 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Gastroenterol. Aug 21, 2007; 13(31): 4255-4259
Published online Aug 21, 2007. doi: 10.3748/wjg.v13.i31.4255
Apoptotic effect of Epigallocatechin-3-gallate on the human gastric cancer cell line MKN45 via activation of the mitochondrial pathway
Zhi-Hua Ran, Qi Xu, Jin-Lu Tong, Shu-Dong Xiao
Zhi-Hua Ran, Qi Xu, Jin-Lu Tong, Shu-Dong Xiao, Department of Gastroenterology, Renji Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai Institute of Digestive Disease, Shanghai 200001, China
Author contributions: All authors contributed equally to the work.
Supported by a grant from Shanghai Leading Academic Discipline Project, No.Y0205
Correspondence to: Zhi-Hua Ran, PhD, Department of Gastroenterology, Renji Hospital, Shanghai Institute of Digestive Disease, Shanghai 200001, China. z-ran@online.sh.cn
Telephone: +86-13801868827 Fax: +86-21-63266027
Received: February 3, 2007
Revised: April 23, 2007
Accepted: April 26, 2007
Published online: August 21, 2007
Abstract

AIM: To investigate whether Epigallocatechin-3-gallate (EGCG) can induce apoptosis of the gastric cancer cell line MKN45 and its apoptotic pathway.

METHODS: To determine this, apoptotic rates of MKN45 cells after EGCG treatment with or without caspase-3 inhibitor were evaluated by Annexin V-FITC + PI staining The influence of EGCG on the activity of caspase-3 in the MKN45 cells was determined by ELISA. By Rhodamine123 staining, the membrane potential change of the mitochondrion was also investigated, and mRNAs and protein expression of the bcl-2 family were analyzed by RT-PCR and Western blot.

RESULTS: EGCG can induce apoptosis of MKN45 cells in time- and dose-dependent manner. Eight hours after EGCG treatment, the activity of caspase-3 in the MKN45 increased, especially 12 h after treatment. The mitochondrial membrane potential was significantly weakened 4 h after EGCG insult. The mRNA and protein expression levels of pro-apoptotic members, such as Bax, Bid and Bad, were upregulated gradually as treated time increased. Moreover, the mRNA and protein expression levels of anti-apoptotic members, such as Bcl-xL and Bcl-2, were inhibited.

CONCLUSION: These data support that EGCG can induce apoptosis of the human gastric cancer cell line MKN45, and the effect is in a time- and dose-dependent manner. The apoptotic pathway triggered by EGCG in MKN45 is mitochondrial-dependent.

Keywords: Epigallocatechin-3-gallate; Stomach neoplasms; Bcl-2; Apoptosis