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
相关论文
共 50 条
  • [21] Regulation of Vascular Injury and Repair by P21-Activated Kinase 1 and P21-Activated Kinase 2: Therapeutic Potential and Challenges
    Han, Chuting
    Zhu, Mengying
    Liu, Yiting
    Yang, Yan
    Cheng, Jun
    Li, Pengyun
    BIOMOLECULES, 2024, 14 (12)
  • [22] Targeting p21-activated kinase 1 for development of a novel anti-arrhythmic drug class
    He, Yu
    Grassam-Rowe, Alexander
    Lei, Ming
    Bae, James S. H.
    PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2023, 378 (1879)
  • [23] Novel Combination Therapy Targeting Oncogenic Signaling Kinase P21-Activated Kinase 1 and Chemotherapeutic Drugs Against Triple-Negative Breast Cancer
    Ezhil, Inemai
    Seetharaman, Abirami
    Kanumuri, Rahul
    Rajamani, Barathidasan
    Gangavarapu, Ranga Rao
    Venkatraman, Ganesh
    Rayala, Suresh K.
    MOLECULAR CANCER THERAPEUTICS, 2025, 24 (04) : 576 - 586
  • [24] p21-activated kinase PAK phosphorylates desmin at sites different from those for Rho-assooiated kinase
    Ohtakara, K
    Inada, H
    Goto, H
    Taki, W
    Manser, E
    Lim, L
    Izawa, I
    Inagaki, M
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 272 (03) : 712 - 716
  • [25] Increased expression of p21-activated kinase in adenomyosis
    Kim, So Ra
    Kim, Sung Hoon
    Lee, Hoi Woul
    Chae, Hee Dong
    Kim, Chung-Hoon
    Kang, Byung Moon
    FERTILITY AND STERILITY, 2010, 94 (03) : 1125 - 1128
  • [26] Interaction of paxillin with p21-activated kinase (PAK)
    Hashimoto, S
    Tsubouchi, A
    Mazaki, Y
    Sabe, H
    MOLECULAR BIOLOGY OF THE CELL, 2000, 11 : 172A - 173A
  • [27] Activation of p21-activated kinase (γ-PAK) by sphingosine
    Tuazon, PT
    Roig, J
    Gatti, A
    Traugh, JA
    FASEB JOURNAL, 1999, 13 (07): : A1490 - A1490
  • [28] Phosphorylation of RhoGDI by p21-activated kinase 1
    DerMardirossian, CM
    Bokoch, GM
    METHODS IN ENZYMOLOGY, VOL 406, REGULATORS AND EFFECTORS OF SMALL GTPASES: RHO FAMILY, 2006, 406 : 80 - 90
  • [29] The mechanism of p21-activated kinase 2 autoactivation
    Wu, H
    Wang, ZX
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (43) : 41768 - 41778
  • [30] P21-activated kinase in inflammatory and cardiovascular disease
    Taglieri, Domenico M.
    Ushio-Fukai, Masuko
    Monasky, Michelle M.
    CELLULAR SIGNALLING, 2014, 26 (09) : 2060 - 2069