Modeling the cancer patient with genetically engineered mice: Prediction of toxicity from molecule-targeted therapies

被引:37
作者
Roberts, RB
Arteaga, CL
Threadgill, DW [1 ]
机构
[1] Univ N Carolina, Dept Genet, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Lineberger Canc Ctr, Chapel Hill, NC 27599 USA
[3] Vanderbilt Univ, Sch Med, Dept Med, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Sch Med, Dept Canc Biol, Nashville, TN 37232 USA
[5] Vanderbilt Univ, Sch Med, Vanderbilt Ingram Canc Ctr, Nashville, TN 37232 USA
关键词
D O I
10.1016/S1535-6108(04)00032-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Current trends foretell the use of cancer treatments customized to each patient. Genetic and molecular profiling of tumors and an increasing number of molecule-targeted therapies contribute to making this a reality. However, as targets of anticancer therapies become specific proteins or pathways, unanticipated side effects may emerge. In addition, the chronic use of these treatments may contribute to the development of degenerative toxicity not predicted by short-term clinical trials. Here we review and propose how genetically engineered mouse models can serve as valuable tools to predict targeted therapy toxicity, as well as to identify allelic variants that predispose individuals to side effects.
引用
收藏
页码:115 / 120
页数:6
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