Targeting the BMK1 MAP Kinase Pathway in Cancer Therapy

被引:24
|
作者
Yang, Qingkai [1 ]
Lee, Jiing-Dwan [1 ]
机构
[1] Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USA
关键词
ACTIVATED PROTEIN-KINASE; SIGNAL-REGULATED KINASE-5; EPIDERMAL-GROWTH-FACTOR; BREAST-TUMOR KINASE; CELL-PROLIFERATION; ENDOTHELIAL-CELLS; TYROSINE KINASES; OXIDATIVE STRESS; GENE-EXPRESSION; C-SRC;
D O I
10.1158/1078-0432.CCR-10-2504
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The big mitogen activated protein kinase 1 (BMK1) pathway is the most recently discovered and least-studied mammalian mitogen-activated protein (MAP) kinase cascade, ubiquitously expressed in all types of cancer cells tested so far. Mitogens and oncogenic signals strongly activate this cellular MAP kinase pathway, thereby passing down proliferative, survival, chemoresistance, invasive, and angiogenic signals in tumor cells. Recently, several pharmacologic small molecule inhibitors of this pathway have been developed. Among them, the BMK1 inhibitor XMD8-92 blocks cellular BMK1 activation and significantly suppresses tumor growth in lung and cervical tumor models and is well tolerated in animals. On the other hand, MEK5 inhibitors, BIX02188, BIX02189, and compound 6, suppress cellular MEK5 activity, but no data exist to date on their effectiveness in animals. Clin Cancer Res; 17(11); 3527-32. (C)2011 AACR.
引用
收藏
页码:3527 / 3532
页数:6
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