Targeting RhoA/Rho Kinase and p21-Activated Kinase Signaling to Prevent Cancer Development and Progression

被引:26
|
作者
Chang, Yu-Wen E. [1 ]
Bean, Ronald R. [1 ]
Jakobi, Rolf [1 ]
机构
[1] Kansas City Univ Med & Biosci, Kansas City, MO 64106 USA
关键词
Cancer invasion; metastasis; RhoA; Rho kinase; ROCK; p21-activated kinase; PAK; adherens junctions; cell motility; apoptosis; anoikis; SQUAMOUS-CELL CARCINOMA; GTP-BINDING PROTEIN; GERANYLGERANYLTRANSFERASE-I INHIBITOR; ANCHORAGE-INDEPENDENT GROWTH; HUMAN PANCREATIC-CANCER; RHO-GTPASES; EPITHELIAL-CELLS; TUMOR-CELLS; GENE-EXPRESSION; GAMMA-PAK;
D O I
10.2174/157489209788452830
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Elevated RhoA/Rho kinase and p21-activated kinase signaling have been shown to promote cancer development and metastasis and have drawn much attention as potential targets of anti-cancer therapy. Elevated RhoA and Rho kinase activity promote cancer cell invasion and eventually lead to metastasis by disrupting E-cadherin-mediated adherens junctions and degradation of the extracellular matrix. Elevated p21-activated kinase activity promotes invasion by stimulating cell motility but also promotes cancer cell survival and growth. In this review we describe normal functions of RhoA/Rho kinase and p21-activated kinase signaling, mechanisms that lead to constitutive activation of RhoA/Rho kinase and p21-activated kinase pathways, and processes by which constitutive RhoA/Rho kinase and p21-activated kinase activity promote cancer development and progression to more aggressive and metastatic phenotypes. In addition, we summarize relevant patents on RhoA/Rho kinase and p21-activated kinase as targets of anti-cancer therapy and discuss the clinical potential of different approaches to modulate RhoA/Rho kinase and p21-activated kinase signaling.
引用
收藏
页码:110 / 124
页数:15
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