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Departments of Pathology [W. S. S.] and Family and Preventive Medicine [K. C., M. L. S.], Division of Research [D. S.], Kaiser Permanente Medical Care Program, Oakland, California, and Sequencing Core Facility [M. R.], Department of Human Genetics [M. L.], University of Utah Health Sciences Center, Salt Lake City, Utah 84132
Some previous studies have demonstrated significant results between
Ki-ras mutations and tumor stage, survival, and/or other
clinical variables, whereas others have not. We therefore evaluated the
significance of codons 12 and 13 Ki-ras mutations in a
large population-based study of 1413 individuals with colon cancer.
Ki-ras mutations were identified in
32% of tumors.
Codon 12 mutations were significantly more common in proximal than
distal tumors (29.1% versus 20.5%;
P < 0.01) and in tumors of advanced stage. Tumors
from men were more likely to have transition mutations and codon 12
G
A mutations. After adjusting for age and stage, the codon 13 G
A
mutation was associated with a 40% (95% confidence interval,
0.952.0) increase in short-term mortality from colon cancer. In
conclusion, this population-based study demonstrates important
relationships between Ki-ras mutations and stage,
survival, tumor location, and gender.
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