Genetic prognostic and predictive markers in colorectal cancer

被引:534
作者
Walther, Axel [2 ,3 ,4 ]
Johnstone, Elaine [1 ]
Swanton, Charles [2 ,4 ]
Midgley, Rachel [1 ]
Tomlinson, Ian [3 ]
Kerr, David [1 ,5 ]
机构
[1] Univ Oxford, Dept Clin Pharmacol, Oxford OX3 7DQ, England
[2] Royal Marsden Hosp, Dept Med, Sutton SM2 5PT, Surrey, England
[3] Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
[4] London Res Inst, London WC2A 3PX, England
[5] Qatar Fdn, Sidra Med & Res Ctr, Doha, Qatar
关键词
ISLAND METHYLATOR PHENOTYPE; GENOME-WIDE ASSOCIATION; MICROSATELLITE INSTABILITY PREDICTS; GROWTH-FACTOR RECEPTOR; KIRSTEN RAS MUTATIONS; III COLON-CANCER; THYMIDYLATE-SYNTHASE; STAGE-II; EXPRESSION PROFILES; CHROMOSOMAL INSTABILITY;
D O I
10.1038/nrc2645
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite many studies of the likely survival outcome of individual patients with colorectal cancer, our knowledge of this subject remains poor. Until recently, we had virtually no understanding of individual responses to therapy, but the discovery of the KRAS mutation as a marker of probable failure of epidermal growth factor receptor (EGFR)-targeted therapy is a first step in the tailoring of treatment to the individual. With the application of molecular analyses, as well as the ability to perform high-throughput screens, there has been an explosive increase in the number of markers thought to be associated with prognosis and treatment outcome in this disease. In this Review, we attempt to summarize the sometimes confusing findings, and critically assess those markers already in the public domain.
引用
收藏
页码:489 / 499
页数:11
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