K-ras mutations in incident sporadic colorectal adenomas

被引:23
作者
Barry, ELR
Baron, JA
Grau, MV
Wallace, K
Haile, RW
机构
[1] Dartmouth Coll Sch Med, Dept Community & Family Med, Sect Biostat & Epidemiol, Evergreen Ctr, Lebanon, NH 03766 USA
[2] Dartmouth Coll Sch Med, Dept Med, Lebanon, NH 03766 USA
[3] Univ So Calif, Dept Prevent Med, Los Angeles, CA 90089 USA
关键词
K-ras; mutation; genotype; colorectal; adenoma;
D O I
10.1002/cncr.21721
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Although K-ras is the most frequently mutated protooncogene in colorectal carcinoma, the specific role and timing of K-ras mutations in colorectal carcinogenesis remains controversial. In the current study, the authors investigated associations with K-ras mutation in incident sporadic colorectal adenomas that occurred during a chemoprevention trial of calcium supplementation. METHODS. K-ras genotyping was performed on 303 colorectal adenomas that were removed from 207 participants during the follow-up phase of the Calcium Polyp Prevention Study. Mutations in codons 12 or 13 of K-ras were detected by denaturing high-performance liquid chromatography and were confirmed by direct sequencing. RESULTS. The adenomas analyzed had a mean estimated size of 0.5 cm, and 3.0% were identified with mutations (95% confidence interval [95% CI], 1.3-4.4%). These mutations were more common in larger adenomas (risk ratio [RR], 12.7 for tumors that measured > 0.5 cm vs. <= 0.5 cm; 95% CI, 2.7-59.7), in adenomas with more advanced histology (RR, 20.6 for tubulovillous/villous vs. tubular; 95% CI, 4.4-96.0), and in adenomas that were located in the rectum compared with the colon (RR, 8.4; 95% CI, 2.3-30.5). CONCLUSIONS. Compared with previous studies, the Current analysis was novel, because it focused on incident adenomas that were diagnosed within a few years of a previous "clean" colonoscopy. The results provided evidence for a very low rate of K-ras mutation among these small, early adenomas and strong support for a role of K-ras mutations in adenoma progression.
引用
收藏
页码:1036 / 1040
页数:5
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