From basic research to clinical development of MEK1/2 inhibitors for cancer therapy

被引:196
作者
Fremin, Christophe
Meloche, Sylvain [1 ]
机构
[1] Univ Montreal, Inst Rech Immunol & Cancerol, Montreal, PQ H3C 3J7, Canada
关键词
SIGNAL-REGULATED KINASE; GROWTH-FACTOR RECEPTOR; T-CELL PROLIFERATION; PROTEIN-KINASE; AZD6244; ARRY-142886; EPIDERMAL-GROWTH; IN-VIVO; B-RAF; CYTOPLASMIC LOCALIZATION; DIFFERENTIAL REGULATION;
D O I
10.1186/1756-8722-3-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Ras-dependent Raf/MEK/ERK1/2 mitogen-activated protein (MAP) kinase signaling pathway is a major regulator of cell proliferation and survival. Not surprisingly, hyperactivation of this pathway is frequently observed in human malignancies as a result of aberrant activation of receptor tyrosine kinases or gain-of-function mutations in RAS or RAF genes. Components of the ERK1/2 pathway are therefore viewed as attractive candidates for the development of targeted therapies of cancer. In this article, we briefly review the basic research that has laid the groundwork for the clinical development of small molecules inhibitors of the ERK1/2 pathway. We then present the current state of clinical evaluation of MEK1/2 inhibitors in cancer and discuss challenges ahead.
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页数:11
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