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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.
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页码:110 / 124
页数:15
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