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Inhibiting myosin light chain kinase retards the growth of mammary and prostate cancer cells.

Abstract
We have previously shown that ML-7, which inhibits myosin light chain kinase (MLCK), induces apoptosis in transformed and non-transformed cells. We have extended these studies and found that ML-7 stimulates the ability of etoposide to induce apoptosis in Mm5MT mouse mammary adenocarcinoma cells and Mat-Ly-Lu rat prostate cancer cells in vitro. ML-7 was also found to have a chemopreventive effect using an in vitro mouse mammary organ culture model. In vivo experiments demonstrated that ML-7 retards the growth of mammary tumours in mice and prostate tumours in rats. Moreover, ML-7 significantly stimulates the ability of etoposide to prevent the growth of established mammary tumours in mice and prostate tumours in rats. These results provide evidence for the efficacy of ML-7 as an adjuvant to etoposide in these models and warrants further development.
AuthorsLian-Zhi Gu, Wen-Yang Hu, Nenad Antic, Rajendra Mehta, Jerrold R Turner, Primal de Lanerolle
JournalEuropean journal of cancer (Oxford, England : 1990) (Eur J Cancer) Vol. 42 Issue 7 Pg. 948-57 (May 2006) ISSN: 0959-8049 [Print] England
PMID16574402 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Chemical References
  • Antineoplastic Agents, Phytogenic
  • Azepines
  • Naphthalenes
  • ML 7
  • Etoposide
  • Myosin-Light-Chain Kinase
Topics
  • Adenocarcinoma (drug therapy, pathology)
  • Animals
  • Antineoplastic Agents, Phytogenic (therapeutic use)
  • Apoptosis (drug effects)
  • Azepines (pharmacology)
  • Cell Division
  • Chemotherapy, Adjuvant
  • Etoposide (therapeutic use)
  • Humans
  • Male
  • Mammary Neoplasms, Experimental (drug therapy, pathology)
  • Mice
  • Mice, Inbred BALB C
  • Myosin-Light-Chain Kinase (antagonists & inhibitors)
  • Naphthalenes (pharmacology)
  • Prostatic Neoplasms (drug therapy, pathology)
  • Random Allocation
  • Rats

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