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
相关论文
共 24 条
[1]   Calcium supplements for the prevention of colorectal adenomas [J].
Baron, JA ;
Beach, M ;
Mandel, JS ;
van Stolk, RU ;
Haile, RW ;
Sandler, RS ;
Rothstein, R ;
Summers, RW ;
Snover, DC ;
Beck, GJ ;
Bond, JH ;
Greenberg, ER .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (02) :101-107
[2]  
Bautista D, 1997, CANCER EPIDEM BIOMAR, V6, P57
[3]  
BOS JL, 1989, CANCER RES, V49, P4682
[4]   Superiority of Denaturing High Performance Liquid Chromatography over single-stranded conformation and conformation-sensitive gel electrophoresis for mutation detection in TSC2 [J].
Choy, YS ;
Dabora, SL ;
Hall, F ;
Ramesh, V ;
Niida, Y ;
Franz, D ;
Kasprzyk-Obara, J ;
Reeve, MP ;
Kwiatkowski, DJ .
ANNALS OF HUMAN GENETICS, 1999, 63 :383-391
[5]   Molecular genetics of colorectal cancer [J].
Fearon, ER .
CANCER PREVENTION: FROM THE LABORATORY TO THE CLINIC: IMPLICATIONS OF GENETIC, MOLECULAR, AND PREVENTIVE RESEARCH, 1995, 768 :101-110
[6]   Detection of genetic alterations in the p53 suppressor gene and the k-ras oncogene among different grades of dysplasia in patients with colorectal adenomas [J].
Hosaka, S ;
Aoki, Y ;
Akamatsu, T ;
Nakamura, N ;
Hosaka, N ;
Kiyosawa, K .
CANCER, 2002, 94 (01) :219-227
[7]  
JEN J, 1994, CANCER RES, V54, P5523
[8]  
JIANG W, 1989, ONCOGENE, V4, P923
[9]   Animal products and K-ras codon 12 and 13 mutations in colon carcinomas [J].
Kampman, E ;
Voskuil, DW ;
van Kraats, AA ;
Balder, HF ;
van Muijen, GNP ;
Goldbohm, RA ;
van't Veer, P .
CARCINOGENESIS, 2000, 21 (02) :307-309
[10]  
LLOR X, 1991, CANCER RES, V51, P4305