Restoration of p53/miR-34a regulatory axis decreases survival advantage and ensures Bax-dependent apoptosis of non-small cell lung carcinoma cells

FEBS Lett. 2014 Feb 14;588(4):549-59. doi: 10.1016/j.febslet.2013.11.040. Epub 2014 Jan 18.

Abstract

Tumor-suppressive miR-34a, a direct target of p53, has been shown to target several molecules of cell survival pathways. Here, we show that capsaicin-induced oxidative DNA damage culminates in p53 activation to up-regulate expression of miR-34a in non-small cell lung carcinoma (NSCLC) cells. Functional analyses further indicate that restoration of miR-34a inhibits B cell lymphoma-2 (Bcl-2) protein expression to withdraw the survival advantage of these resistant NSCLC cells. In such a proapoptotic cellular milieu, where drug resistance proteins are also down-regulated, p53-transactivated Bcl-2 associated X protein (Bax) induces apoptosis via the mitochondrial death cascade. Our results suggest that p53/miR-34a regulatory axis might be critical in sensitizing drug-resistant NSCLC cells.

Keywords: Apoptosis; B cell lymphoma-2; Bcl-2 associated X protein; Capsaicin; DNA-damage; MiR-34a; Mitochondrial transmembrane potential; Reactive oxygen species; p53.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis Regulatory Proteins / metabolism
  • Apoptosis* / drug effects
  • Capsaicin / pharmacology*
  • Carcinoma, Non-Small-Cell Lung / genetics
  • Carcinoma, Non-Small-Cell Lung / metabolism
  • Carcinoma, Non-Small-Cell Lung / pathology*
  • Caspases / metabolism
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • DNA Damage
  • Drug Resistance, Multiple / drug effects
  • Enzyme Activation / drug effects
  • Humans
  • Lung Neoplasms / genetics
  • Lung Neoplasms / metabolism
  • Lung Neoplasms / pathology*
  • MicroRNAs / genetics*
  • Mitochondria / drug effects
  • Reactive Oxygen Species / metabolism
  • Transcriptional Activation / drug effects
  • Tumor Suppressor Protein p53 / metabolism*
  • Up-Regulation / drug effects
  • bcl-2-Associated X Protein / genetics
  • bcl-2-Associated X Protein / metabolism*

Substances

  • Apoptosis Regulatory Proteins
  • MIRN34 microRNA, human
  • MicroRNAs
  • Reactive Oxygen Species
  • Tumor Suppressor Protein p53
  • bcl-2-Associated X Protein
  • Caspases
  • Capsaicin