Low somatic K-ras mutation frequency in colorectal cancer diagnosed under the age of 45 years

被引:32
作者
Alsop, Kathryn
Mead, Leeanne
Smith, Letitia D.
Royce, Simon G.
Tesoriero, Andrea A.
Young, Joanne P.
Haydon, Andrew
Grubb, Garry
Giles, Graham G.
Jenkins, Mark A.
Hopper, John L. [1 ]
Southey, Melissa C.
机构
[1] Univ Melbourne, Ctr Mol Environm Genet & Analyt Epidemiol, Parkville, Vic 3052, Australia
[2] Univ Melbourne, Genet Epidemiol Lab, Dept Pathol, Parkville, Vic 3052, Australia
[3] Queensland Inst Med Res, Mol Canc Epidemiol Lab, Brisbane, Qld 4006, Australia
[4] Monash Univ, Dept Epidemiol & Prevent Med, Clayton, Vic 3168, Australia
[5] Int Agcy Res Canc, Lyon, France
关键词
early-onset colorectal cancer; K-ras mutations;
D O I
10.1016/j.ejca.2006.02.023
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Somatic mutation of K-ras is known to be a common event in colorectal cancer tumourigenesis however its association with age at onset has not been widely explored. in this study, we have analyzed tumours from a population-based study of colorectal cancer diagnosed before the age of 45 years, in which cases had been previously screened for germ-line mismatch repair gene mutations and for microsatellite instability. We used a micro-dissection and sequencing approach to search for somatic K-ras mutations in codons 12, 13 and 61 in 101 early-onset colorectal cancers. Six (6%) somatic K-ras mutations were detected; five in codon 12 (4 G > T transitions and 1 G > A) and one in codon 13 (G > A transition). All codon 12 mutations were identified in microsatellite stable tumours and the codon 13 mutation was identified in a MSI-high tumour. Four cases with K-ras mutations had no reported family history of colorectal cancer and two had some family history of colorectal cancer. None were known to carry a germ-line mutation in hMSH2, hMLH1, hMSH6 or hPMS2. The role of somatic K-ras mutations in early-onset colorectal cancer carcinogenesis appears to be minor, in contrast to its significant role in colorectal. cancer of later age of onset. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1357 / 1361
页数:5
相关论文
共 23 条
[1]   Kirsten ras mutations in patients with colorectal cancer:: the 'RASCAL II' study [J].
Andreyev, HJN ;
Norman, AR ;
Cunningham, D ;
Oates, J ;
Dix, BR ;
Iacopetta, BJ ;
Young, J ;
Walsh, T ;
Ward, R ;
Hawkins, N ;
Beranek, M ;
Jandik, P ;
Benamouzig, R ;
Jullian, E ;
Laurent-Puig, P ;
Olschwang, S ;
Muller, O ;
Hoffmann, I ;
Rabes, HM ;
Zietz, C ;
Troungos, C ;
Valavanis, C ;
Yuen, ST ;
Ho, JWC ;
Croke, CT ;
O'Donoghue, DP ;
Giaretti, W ;
Rapallo, A ;
Russo, A ;
Bazan, V ;
Tanaka, M ;
Omura, K ;
Azuma, T ;
Ohkusa, T ;
Fujimori, T ;
Ono, Y ;
Pauly, M ;
Faber, C ;
Glaesener, R ;
de Goeij, AFPM ;
Arends, JW ;
Andersen, SN ;
Lövig, T ;
Breivik, J ;
Gaudernack, G ;
Clausen, OPF ;
De Angelis, P ;
Meling, GI ;
Rognum, TO ;
Smith, R .
BRITISH JOURNAL OF CANCER, 2001, 85 (05) :692-696
[2]   Kirsten ras mutations in patients with colorectal cancer: the multicenter "RASCAL" study [J].
Andreyev, HJN ;
Norman, AR ;
Cunningham, D ;
Oates, JR ;
Clarke, PA .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (09) :675-684
[3]  
Armes JE, 1999, CANCER RES, V59, P2011
[4]  
BOLAND CR, 1998, CANCER RES, V58, P5428
[5]  
BOS JL, 1990, CANCER RES, V50, P1352
[6]   GENETIC MECHANISMS IN TUMOR INITIATION AND PROGRESSION .10. THE RAS GENE FAMILY AND HUMAN CARCINOGENESIS [J].
BOS, JL .
MUTATION RESEARCH, 1988, 195 (03) :255-271
[7]  
BOS JL, 1989, CANCER RES, V49, P4682
[8]   K-ras oncogene mutations in sporadic colorectal cancer in The Netherlands Cohort Study [J].
Brink, M ;
de Goeij, AFPM ;
Weijenberg, MP ;
Roemen, GMJM ;
Lentjes, MHFM ;
Pachen, MMM ;
Smits, KM ;
de Bruïne, AP ;
Goldbohm, RA ;
van den Brandt, PA .
CARCINOGENESIS, 2003, 24 (04) :703-710
[9]   DIFFERENT BASE BASE MISPAIRS ARE CORRECTED WITH DIFFERENT EFFICIENCIES AND SPECIFICITIES IN MONKEY KIDNEY-CELLS [J].
BROWN, TC ;
JIRICNY, J .
CELL, 1988, 54 (05) :705-711
[10]   A GENETIC MODEL FOR COLORECTAL TUMORIGENESIS [J].
FEARON, ER ;
VOGELSTEIN, B .
CELL, 1990, 61 (05) :759-767