Direct regulation of caspase‑3 by the transcription factor AP‑2α is involved in aspirin‑induced apoptosis in MDA‑MB‑453 breast cancer cells

Mol Med Rep. 2013 Mar;7(3):909-14. doi: 10.3892/mmr.2013.1257. Epub 2013 Jan 2.

Abstract

Aspirin has been reported to trigger apoptosis in various cancer cell lines. However, the detailed mechanisms involved remain elusive. The present study aimed to investigate whether aspirin plays a role in apoptosis of MDA-MB-453 cells. The effect of aspirin on the proliferation of human MDA-MB-453 cells breast cancer cells was evaluated using MTT assay, flow cytometry and western blotting. The present study reports that aspirin induces the apoptosis of MDA‑MB‑453 breast cancer cells which was attributed to the increased expression and activation of caspase‑3. Moreover, AP‑2α, a transcription factor highly expressed in MDA‑MB‑453 cells, was identified as a negative regulator of caspase‑3 transcription and AP‑2α was attenuated following aspirin treatment. Therefore, aspirin may increase the expression of caspase‑3 by inducing the degradation of AP‑2α, which increases activated caspase‑3 expression, thereby triggering apoptosis in MDA‑MB‑453 cells. Thus, aspirin may be used in breast cancer therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / toxicity*
  • Apoptosis / drug effects*
  • Aspirin / toxicity*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Caspase 3 / genetics
  • Caspase 3 / metabolism*
  • Cell Line, Tumor
  • Female
  • Humans
  • Promoter Regions, Genetic
  • Proteasome Endopeptidase Complex / metabolism
  • Protein Binding
  • RNA Interference
  • RNA, Small Interfering / metabolism
  • Transcription Factor AP-2 / antagonists & inhibitors
  • Transcription Factor AP-2 / genetics
  • Transcription Factor AP-2 / metabolism*
  • Up-Regulation / drug effects

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • RNA, Small Interfering
  • Transcription Factor AP-2
  • Caspase 3
  • Proteasome Endopeptidase Complex
  • Aspirin