4.5 Article

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

期刊

FEBS LETTERS
卷 588, 期 4, 页码 549-559

出版社

WILEY
DOI: 10.1016/j.febslet.2013.11.040

关键词

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

资金

  1. University Grant Commission (UGC)
  2. Department of Biotechnology (DBT)
  3. Council for Scientific and Industrial Research (CSIR)
  4. Department of Science and Technology (DST), Govt. of India

向作者/读者索取更多资源

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-trans-activated 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. (C) 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

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