Targeting MAPK signalling: Prometheus' fire or pandora's box?

被引:55
作者
Boldt, S
Kolch, W
机构
[1] Beatson Inst Canc Res, Glasgow G61 1BD, Lanark, Scotland
[2] Univ Glasgow, Inst Biomed & Life Sci, Glasgow G12 8QQ, Lanark, Scotland
关键词
mitogen activated protein kinase; ERK; JNK; p38; signal transduction; drug discovery; clinical trials;
D O I
10.2174/1381612043384420
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
MAPK (Mitogen Activated Protein Kinase) pathways mediate fundamental biological processes and have moved into the limelight of drug discovery during the past decade. Here we review the biochemistry and biology of MAPK signalling with a focus on ERK, JNK and p38. We summarise current drug discovery efforts and clinical trials. Further, we critically discuss the rationale behind current strategies of using MAPK pathways as drug targets and suggest new approaches that take the complexity of MAPK signalling networks into account.
引用
收藏
页码:1885 / 1905
页数:21
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