[Aspirin inhibits the proliferation of breast cancer cells via inducing apoptosis and autophagy]

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2017 Oct;33(10):1348-1353.
[Article in Chinese]

Abstract

Objective To explore the effect of aspirin on the apoptosis and autophagy of human epidermal growth factor receptor 2 (HER2)-positive AU-565 breast cancer cells and triple negative MDA-MB-231 breast cancer cells. Methods MTT assay was performed to detect the effect of aspirin on cell proliferation of cancer cells; flow cytometry was performed to assess the effect of aspirin on cell apoptosis; Western blotting was used to determine the protein expressions of apoptosis-related proteins Bcl2, cleaved caspase-3 (c-caspase-3), cleaved PARP (c-PARP) and autophagy-related gene 3 (ATG3), LC3A, LC3B. Results Aspirin inhibited the proliferation of AU-565 and MDA-MB-231 cells and increased the cell apoptosis. The expressions of c-caspase-3 and c-PARP were up-regulated, the Bcl2 was down-regulated, and ATG3, LC3A, LC3B were also significantly up-regulated. Conclusion Aspirin can inhibit the proliferation of AU-565 and MDA-MB-231 breast cancer cells via inducing cell apoptosis and autophagy.

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Apoptosis / drug effects*
  • Aspirin / pharmacology*
  • Autophagy / drug effects*
  • Autophagy-Related Proteins / metabolism
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Caspase 3 / metabolism
  • Cell Line, Tumor
  • Cell Proliferation / drug effects*
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Microtubule-Associated Proteins / metabolism
  • Poly(ADP-ribose) Polymerases / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Time Factors
  • Ubiquitin-Conjugating Enzymes / metabolism

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Autophagy-Related Proteins
  • BCL2 protein, human
  • MAP1LC3B protein, human
  • Microtubule-Associated Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Ubiquitin-Conjugating Enzymes
  • Poly(ADP-ribose) Polymerases
  • Caspase 3
  • ATG3 protein, human
  • Aspirin