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Am J Physiol Gastrointest Liver Physiol 282: G932-G936, 2002. First published January 30, 2002; doi:10.1152/ajpgi.00312.2001
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Vol. 282, Issue 6, G932-G936, June 2002

Age-associated loss of heterozygosity of tumor suppressor genes in the gastric mucosa of humans

Lathika Moragoda1, Richard Jaszewski1,2, Prasad Kulkarni1, and Adhip P. N. Majumdar1,2,3,4

2 Veterans Affairs Medical Center, Departments of 1 Internal Medicine and 3 Biochemistry and Molecular Biology, and 4 Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, Michigan 48201

The current study is based on the hypothesis that aging predisposes gastric mucosa to carcinogenesis through altered expression and/or mutations of genes involved in cell growth. To test this hypothesis, we investigated the age-associated changes in mutation of adenomatous polyposis coli (APC), deleted in colorectal cancer (DCC), p53, and K-ras genes in the gastric mucosa of 19 healthy subjects of varying ages (25-91 yr). Specifically, we studied the loss of heterozygosity (LOH) of these genes in cardia, body, and antrum of the stomach. We observed that 3 of 19 subjects (16%) over 60 yr of age show LOH of at least one of the tumor suppressor genes. Among the subjects over 60 yr of age, the incidence of LOH is 38% (3/8). Two of three subjects had mutations in more than one tumor suppressor gene. In all three affected subjects, mutation in APC, DCC, or p53 was located mainly in the body of the stomach, suggesting increased susceptibility of this region to neoplastic changes. However, no LOH of K-ras was observed in these subjects. Our observation that subjects over 60 yr of age show mutation in one or more of the tumor suppressor genes suggests an age-related increase in predisposition of the stomach to neoplasia.

aging; mutations; p53; adenomatous polyposis coli; deleted in colorectal cancer; K-ras; neoplasia





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