Using genome-wide mapping in the mouse to identify genes that influence drug response

被引:11
作者
Watters, JW
McLeod, HL
机构
[1] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[2] Washington Univ, Dept Genet, Siteman Canc Ctr, Sch Med, St Louis, MO 63110 USA
[3] Washington Univ, Dept Mol Biol & Pharmacol, Siteman Canc Ctr, Sch Med, St Louis, MO 63110 USA
关键词
QUANTITATIVE TRAIT LOCI; STRAIN DIFFERENCES; MICE; ANTINOCICEPTION; PHARMACOGENOMICS; CYCLOPHOSPHAMIDE; METABOLISM; TOXICITY; LIVER;
D O I
10.1016/S0165-6147(02)00044-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Differential drug response is most often likely to be a complex trait, controlled by the combined influences of multiple genes and environmental influences. As a result of theoretical and technical limitations, to date, most clinically useful pharmacogenomic studies in humans have been limited to a small number of candidate genes that have a relatively major impact on drug response. Here, the problems involved in identifying genes that underlie drug response in humans are discussed and the power of mouse genetics as a tool for pharmacogenomic discovery is highlighted.
引用
收藏
页码:55 / 58
页数:4
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