Notch signaling, γ-secretase inhibitors, and cancer therapy

被引:355
作者
Shih, Ie-Ming
Wang, Tian-Li
机构
[1] Johns Hopkins Med Inst, Dept Gynecol, Baltimore, MD 21231 USA
[2] Johns Hopkins Med Inst, Dept Oncol, Baltimore, MD 21231 USA
[3] Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21231 USA
关键词
TRANSGENIC MICE; ACTIVATION; TUMOR; TARGET; CELLS; LEUKEMIA/LYMPHOMA; OVEREXPRESSION; PRESENILIN; MUTATIONS;
D O I
10.1158/0008-5472.CAN-06-3958
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Notch signaling pathway represents a critical component in the molecular circuits that control cell fate during development. Aberrant activation of this pathway contributes to tumorigenesis. The role of Notch in human cancer has been highlighted recently by the presence of activating mutations and amplification of Notch genes in human cancer and by the demonstration that genes in the Notch signaling pathway could be potential therapeutic targets. It has become clear that one of the major therapeutic targets in the Notch pathway are the Notch receptors, in which T-secretase inhibitors prevent the generation of the oncogenic (intracellular) domain of Notch molecules and suppress the Notch activity. This review article summarizes the biological roles of Notch molecules in cancer development with special emphasis on the promise and challenges in applying gamma-secretase inhibitors as a new line of targeted therapeutic agents.
引用
收藏
页码:1879 / 1882
页数:4
相关论文
共 25 条
[21]   Notch3 gene amplification in ovarian cancer [J].
Park, Joon T. ;
Li, Mei ;
Nakayama, Kentaro ;
Mao, Tsui-Lien ;
Davidson, Ben ;
Zhang, Zhen ;
Kurman, Robert J. ;
Eberhart, Charles G. ;
Shih, Ie-Ming ;
Wang, Tian-Li .
CANCER RESEARCH, 2006, 66 (12) :6312-6318
[22]   Deficient T cell fate specification in mice with an induced inactivation of Notch1 [J].
Radtke, F ;
Wilson, A ;
Stark, G ;
Bauer, M ;
van Meerwijk, J ;
MacDonald, HR ;
Aguet, M .
IMMUNITY, 1999, 10 (05) :547-558
[23]   Notch and presenilin: Regulated intramembrane proteolysis links development and degeneration [J].
Selkoe, D ;
Kopan, R .
ANNUAL REVIEW OF NEUROSCIENCE, 2003, 26 :565-597
[24]   Notch/γ-secretase inhibition turns proliferative cells in intestinal crypts and adenomas into goblet cells [J].
van Es, JH ;
van Gijn, ME ;
Riccio, O ;
van den Born, M ;
Vooijs, M ;
Begthel, H ;
Cozijnsen, M ;
Robine, S ;
Winton, DJ ;
Radtke, F ;
Clevers, H .
NATURE, 2005, 435 (7044) :959-963
[25]   Crosstalk between tumor and endothelial cells promotes tumor angiogenesis by MAPK activation of Notch signaling [J].
Zeng, QH ;
Li, SL ;
Chepeha, DB ;
Giordano, TJ ;
Li, J ;
Zhang, HL ;
Polverini, PJ ;
Nor, J ;
Kitajewski, J ;
Wang, CY .
CANCER CELL, 2005, 8 (01) :13-23