Gastric Cancer
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Mar 15, 2003; 9(3): 437-441
Published online Mar 15, 2003. doi: 10.3748/wjg.v9.i3.437
Studies on microsatellite instability in p16 gene and expression of hMSH2 mRNA in human gastric cancer tissues
Qin-Xian Zhang, Yi Ding, Xiao-Ping Le, Peng Du
Qin-Xian Zhang, Yi Ding, Xiao-Ping Le, Molecular Cell Biology Research Center, Medical College of Zhengzhou University; Zhengzhou 450052, Henan Province, China
Peng Du, Henan Key Lab. of Molecular Medicine, Zhengzhou 450052, Henan Province, China
Author contributions: All authors contributed equally to the work.
Supported by the National Natural Science Foundation of China, No. 39170440
Correspondence to: Pro. Qin-Xian Zhang, Molecular Cell Biology Research Center, Medical College of Zhengzhou University; 40 Daxue Lu, Zhengzhou 450052, Henan Province, China. qxz53@zzu.edu.cn
Telephone: +86-371-6977002 Fax: +86-371-6977002
Received: September 13, 2002
Revised: October 8, 2002
Accepted: October 29, 2002
Published online: March 15, 2003
Abstract

AIM: To detect the loss of heterozygosity (LOH) frequency of microsatellite sites D9s171, D9s1604 of p16 gene and expression of hMSH2 mRNA in various differentiated types of gastric cancer, adjacent cancer tissues and normal gastric mucosa.

METHODS: LOH was detected by polymerase chain reaction (PCR)-denaturing polyacrylamide gel electrophoresis-silver staining. The expression of hMSH2 mRNA was examined with in situ hybridization.

RESULTS: The frequency rate of LOH was significantly higher in gastric cancers than that in adjacent cancer tissues (P = 0.032). No significant difference was noted among various differentiated types and various clinical stages of gastric cancers. The significantly reduced expression of hMSH2 mRNA positive signal cells exhibited in gastric cancers, in comparison with that in the adjacent cancer tissues and normal gastric mucosa, respectively (P = 0.001). No significant difference was noted among various clinical stages of gastric cancers (P > 0.05). The difference of positive signal cells in poorly differentiated cancers and those in well and moderately differentiated cancers were significant (P < 0.001).

CONCLUSION: The frequencies of LOH in two microsatellite sites, D9s171 and D9s1604, in p16 genome were associated with development of gastric cancer and no significant correlation was demonstrated between the LOH frequency and the cell differentiated types of tumor cells or clinical stages. There was a positive relationship between the expression of hMSH2 mRNA and the differentiated types of gastric cancer.

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