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
相关论文
共 50 条
  • [31] Development of anticancer drugs targeting the MAP kinase pathway
    Sebolt-Leopold, JS
    ONCOGENE, 2000, 19 (56) : 6594 - 6599
  • [32] Development of anticancer drugs targeting the MAP kinase pathway
    Judith S Sebolt-Leopold
    Oncogene, 2000, 19 : 6594 - 6599
  • [33] Targeting the Extracellular Signal-Regulated Kinase Pathway in Cancer Therapy
    Kohno, Michiaki
    Tanimura, Susumu
    Ozaki, Kei-ichi
    BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2011, 34 (12) : 1781 - 1784
  • [34] Fluid shear stress activates big MAP kinase (BMK1) in endothelial cells:: Roles of reactive oxygen species (ROS), Ca2+ and tyrosine kinases
    Yan, C
    Takahashi, M
    Lee, JD
    Ulevitch, RJ
    Berk, BC
    FASEB JOURNAL, 1998, 12 (04): : A84 - A84
  • [35] Effect of high glucose on BMK1 activity in rat mesangial cells
    Suzaki, Y
    Yoshizumi, M
    Tsuchiya, K
    Kirima, K
    Kyaw, M
    Tamaki, T
    JAPANESE JOURNAL OF PHARMACOLOGY, 2002, 88 : 210P - 210P
  • [36] Role of BMK1 in regulation of growth factor-induced cellular responses
    Yutaka Kato
    Ta-Hsiang Chao
    Masaaki Hayashi
    Richard I. Tapping
    Jiing-Dwan Lee
    Immunologic Research, 2000, 21 : 233 - 237
  • [37] Targeting the PD-1 Pathway in Cancer Therapy
    Topalian, Suzanne L.
    ONCOLOGIST, 2012, 17 : 6 - 6
  • [38] miR-429 inhibits glioma invasion through BMK1 suppression
    Chen, Weiyi
    Zhang, Baogang
    Guo, Wenjun
    Gao, Linlin
    Shi, Lihong
    Li, Hongli
    Lu, Shijun
    Liu, Yuqing
    Li, Xiaolong
    JOURNAL OF NEURO-ONCOLOGY, 2015, 125 (01) : 43 - 54
  • [39] The MEKK3/MEK5/BMK1 signaling pathway regulates calcineurin activity by phosphorylation of MCIP1
    Abbasi, S
    Yang, JH
    Li, M
    Mi, TJ
    Razeghi, P
    Taegtmeyer, H
    Lee, JD
    Kellems, RE
    Xia, Y
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2005, 38 (05) : 868 - 868
  • [40] High glucose activates BMK1 in cultured rat mesangial cells.
    Suzaki, Y
    Yoshizumi, M
    Ozawa, Y
    Ishizawa, K
    Ali, N
    Tsuchiya, K
    Tamaki, T
    JOURNAL OF PHARMACOLOGICAL SCIENCES, 2003, 91 : 80P - 80P