Targeting ROCK/LIMK/cofilin signaling pathway in cancer

Arch Pharm Res. 2019 Jun;42(6):481-491. doi: 10.1007/s12272-019-01153-w. Epub 2019 Apr 27.

Abstract

Rho-associated coiled-coil-containing protein kinase (ROCK)/Lin11, Isl-1 and Mec-3 kinase (LIMK)/cofilin-signaling cascades are stimulated by receptor tyrosine kinases, G protein-coupled receptors, integrins and its ligands, growth factors, hormones, fibronectin, collagen, and laminin. Activated signaling cascades can cause transit from normal cells to cancer cells by modulating actin/filament dynamics. In various cancers including breast, prostate, and colorectal cancers, high expression or activity of each cascade protein is significantly associated with poor survival rate of patients as well as aggressive metastasis. Silencing ROCK, LIMK, or cofilin can abrogate their activities and inhibit cancer cell growth, invasion, and metastasis. Therefore ROCK/LIMK/cofilin signaling proteins might be good candidates to develop cancer prevention strategies or therapeutics. Currently, netarsudil, a ROCK inhibitor, is only used in clinical patients for glaucoma or ocular hypertension, but not for cancer. In this review, we will discuss comprehensive ROCK/LIMK/cofilin signaling pathway in cancers and its inhibitors for developing cancer therapy.

Keywords: Cancer therapy; Cofilin; Inhibitors; LIMK; ROCK; Signaling pathways.

Publication types

  • Review

MeSH terms

  • Actin Depolymerizing Factors / antagonists & inhibitors
  • Actin Depolymerizing Factors / metabolism
  • Animals
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / therapeutic use
  • Clinical Trials as Topic
  • Drug Evaluation, Preclinical
  • Humans
  • Lim Kinases / antagonists & inhibitors
  • Lim Kinases / metabolism
  • Molecular Targeted Therapy / methods
  • Neoplasms / drug therapy*
  • Neoplasms / pathology
  • Phosphorylation / drug effects
  • Protein Kinase Inhibitors / pharmacology*
  • Protein Kinase Inhibitors / therapeutic use
  • Signal Transduction / drug effects*
  • rho-Associated Kinases / antagonists & inhibitors
  • rho-Associated Kinases / metabolism

Substances

  • Actin Depolymerizing Factors
  • Antineoplastic Agents
  • Protein Kinase Inhibitors
  • Lim Kinases
  • rho-Associated Kinases