[Effects of Quercetin on Autophagy and Phosphatidylinositol 3-kinase/Protein Kinase B/Mammalian Target of Rapamycin Signaling Pathway in Human Prostate Cancer PC-3 Cells]

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2020 Oct;42(5):578-584. doi: 10.3881/j.issn.1000-503X.12361.
[Article in Chinese]

Abstract

Objective To investigate the effects of quercetin on cell viability,apoptosis,autophagy,and phosphatidylinositol 3-kinase(PI3K)/protein kinase B(Akt)/mammalian target of rapamycin(mTOR)signaling pathway in human prostate cell carcinoma PC-3 cells.Methods PC-3 cells were cultured in vitro,and cell viability was detected by CCK-8.Apoptosis was detected by TUNEL staining.Autophagy vesicle was observed by acridine orange staining.Autophagosomes was observed by GFP-LC3 plasmid transfection analysis.Expressions of autophagy-related protein microtubule associated protein 1 light chain 3 fusion protein(LC3)and Beclin-1 and PI3K/Akt/mTOR signaling pathway protein were detected by Western blot analysis.Results Quercetin inhibited cell viability in a dose-time dependent manner and induced apoptosis.Quercetin increased the number of autophagy vesicles and autophagosomes in PC-3 cells.Quercetin increased the expressions of LC3-Ⅱ/LC3-Ⅰ and Beclin-1 in PC-3 cells and decreased the expression of phosphorylated-PI3K,phosphorylated-Akt and phosphorylated-mTOR.Conclusion Quercetin may induce autophagy by inactivating PI3K/Akt/mTOR signaling pathway in PC-3 cells.

Keywords: autophagy; phosphatidylinositol 3-kinase/protein kinase B/mammalian target of rapamycin signaling pathway; prostate cancer; quercetin.

MeSH terms

  • Antioxidants / pharmacology
  • Autophagy* / drug effects
  • Humans
  • Male
  • PC-3 Cells
  • Phosphatidylinositol 3-Kinase* / metabolism
  • Prostatic Neoplasms
  • Proto-Oncogene Proteins c-akt / metabolism
  • Quercetin* / pharmacology
  • Signal Transduction* / drug effects
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Antioxidants
  • Quercetin
  • Phosphatidylinositol 3-Kinase
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases