Cell cycle regulatory protein 5 (Cdk5) is a novel downstream target of ERK in carboplatin induced death of breast cancer cells

Curr Cancer Drug Targets. 2008 Dec;8(8):741-52. doi: 10.2174/156800908786733405.

Abstract

Neuronal cell specific cyclin-dependent kinase 5 (Cdk5) is a known regulator of neurodegenerative disorders such as Alzheimer's and Parkinson's diseases. We report that Cdk5 also plays an important role in the proliferation of breast cancer cells MCF-7 and MDA MB-231 and is functionally involved in chemosensitivity as well as in cell death pathways induced by anti-cancer drug carboplatin (Carb). Here, we demonstrate that carboplatin induced Cdk5 activation under positive regulation of ERK, promotes cell death in MCF-7 and MDA MB-231 cells. DNA-damage stress enhanced ERK activity utilizes Cdk5 as one of its downstream targets for the execution of death signal in carboplatin induced death in MCF-7 and MDA MB-231 cells. Additionally, present data clearly indicates that activated Cdk5 modulates p53 transactivation in MCF-7 cells. However, in p53 mutant MDA MB-231 cells, Cdk5 mediated cell death is likely to be p53 independent. Collectively, our findings not only draw attention to the extra-neuronal functions of Cdk5 but also propose Cdk5 as a novel and potential therapeutic target of chemotherapeutic drugs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects*
  • Breast Neoplasms / enzymology
  • Breast Neoplasms / pathology*
  • Carboplatin / pharmacology*
  • Cell Line, Tumor
  • Cell Proliferation
  • Chloramphenicol O-Acetyltransferase / genetics
  • Cyclin-Dependent Kinase 5 / antagonists & inhibitors*
  • Enzyme Activation
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Humans
  • Immunoprecipitation
  • RNA, Small Interfering

Substances

  • Antineoplastic Agents
  • RNA, Small Interfering
  • Carboplatin
  • Chloramphenicol O-Acetyltransferase
  • Cyclin-Dependent Kinase 5
  • Extracellular Signal-Regulated MAP Kinases