Src and focal adhesion kinase as therapeutic targets in cancer

被引:148
作者
Brunton, Valerie G. [1 ]
Frame, Margaret C. [1 ]
机构
[1] Univ Edinburgh, Div Canc Biol, Inst Genet & Mol Med, Edinburgh EH4 2XR, Midlothian, Scotland
关键词
D O I
10.1016/j.coph.2008.06.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Over the past few years small molecule inhibitors of both Src family kinases and focal adhesion kinase (FAK) have entered clinical studies for the treatment of solid tumours. These adhesion-linked kinases are involved in a number of pathways that have impact on the behaviour of tumour cells and the challenge is now, how to take these forward in the clinical setting.
引用
收藏
页码:427 / 432
页数:6
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