Gastric Cancer
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Apr 15, 2003; 9(4): 655-659
Published online Apr 15, 2003. doi: 10.3748/wjg.v9.i4.655
Mutation and methylation of hMLH1 in gastric carcinomas with microsatellite instability
Dian-Chun Fang, Rong-Quan Wang, Shi-Ming Yang, Jian-Ming Yang, Hai-Feng Liu, Gui-Yong Peng, Tian-Li Xiao, Yuan-Hui Luo
Dian-Chun Fang, Rong-Quan Wang, Shi-Ming Yang, Jian-Ming Yang, Hai-Feng Liu, Gui-Yong Peng, Tian-Li Xiao, Yuan-Hui Luo, Department of Gastroenterology, Southwest Hospital, Third Military Medical University, Chongqing, 400038, China
Author contributions: All authors contributed equally to the work.
Supported by the National Natural Science Foundation of China, No. 30070043, and “10.5” Scientific Research Foundation of Chinese PLA, No. 01Z075
Correspondence to: Dian-Chun Fang, M.D., Ph.D. Southwest Hospital, Third Military Medical University, Chongqing 400038, China. fangdianchun@hotmail.com
Telephone: +86-23-68754624 Fax: +86-23-68754124
Received: October 9, 2002
Revised: November 7, 2002
Accepted: November 14, 2002
Published online: April 15, 2003
Abstract

AIM: To appraise the correlation of mutation and methylation of hMSH1 with microsatellite instability (MSI) in gastric cancers.

METHODS: Mutation of hMLH1 was detected by Two-dimensional electrophoresis (Two-D) and DNA sequencing; Methylation of hMLH1 promoter was measured with methylation-specific PCR; MSI was analyzed by PCR-based methods.

RESULTS: Sixty-eight cases of sporadic gastric carcinoma were studied for mutation and methylation of hMLH1 promoter and MSI. Three mutations were found, two of them were caused by a single bp substitution and one was caused by a 2 bp substitution, which displayed similar Two-D band pattern. Methylation of hMLH1 promoter was detected in 11 (16.2%) gastric cancer. By using five MSI markers, MSI in at least one locus was detected in 17/68 (25%) of the tumors analyzed. Three hMLH1 mutations were all detected in MSI-H (≥ 2 loci, n = 8), but no mutation was found in MSI-L (only one locus, n = 9) or MSS (tumor lacking MSI or stable, n = 51). Methylation frequency of hMLH1 in MSI-H (87.5%, 7/8) was significantly higher than that in MSI-L (11.1%, 1/9) or MSS (5.9%, 3/51) (P < 0.01-0.001), but no difference was found between MSI-L and MSS (P > 0.05).

CONCLUSION: Both mutation and methylation of hMLH1 are involved in the MSI pathway but not related to the LOH pathway in gastric carcinogenesis.

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