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