Characterization of a novel oncogenic K-ras mutation in colon cancer

被引:48
作者
Akagi, Kiwamu
Uchibori, Ryosuke
Yamaguchi, Kensei
Kurosawa, Keiko
Tanaka, Yoichiro
Kozu, Tomoko
机构
[1] Saitama Canc Ctr, Mol Diagnosis & Canc Prevent Div, Kitadachigun, Saitama 3620806, Japan
[2] Saitama Canc Ctr, Div Gastroenterol, Kitadaichigun, Saitama 3620806, Japan
[3] Saitama Canc Ctr, Res Inst Clin Oncol, Kitadachigun, Saitama 3620806, Japan
关键词
K-ras; colorectal cancer; mutation; transformation; signaling;
D O I
10.1016/j.bbrc.2006.11.091
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Activating mutations of RAS are frequently observed in subsets of human cancers, indicating that RAS activation is involved in tumorigenesis. Here, we identified and characterized a novel G to T transversion mutation of the K-ras gene at the third position of codon 19 (TTG) which substituted phenylalanine for leucine in 3 primary colon carcinomas. Biological and biochemical activity was examined using transformed NIH3T3 cells expressing mutant or wild-type K-ras. Transformants harboring the K-ras mutation at codon 19 showed proliferative capacity under serum-starved conditions, less contact inhibition, anchorage-independent growth, tumorigenicity in nude mice and elevation of active Ras-GTP levels. These results indicated that this novel mutation possesses high oncogenic activity. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:728 / 732
页数:5
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