Synergistic Effect of Apigenin and Curcumin on Apoptosis, Paraptosis and Autophagy-related Cell Death in HeLa Cells

Anticancer Res. 2021 Mar;41(3):1271-1282. doi: 10.21873/anticanres.14884.

Abstract

Background/aim: We aimed to investigate the synergistic effects of apigenin and curcumin on the cross-talk between apoptosis and autophagic cell death, as well as on paraptosis in HeLa cells.

Materials and methods: Cell viability was measured using the MTT assay. Synergistic effects were measured using the Bliss independence model. qRT-PCR was used to study the expression of genes related to apoptosis, autophagic cell death, and cross-talk. GRP78/BiP immunostaining was used to identify endoplasmic reticulum (ER) stress.

Results: Treatment with a combination of apigenin and curcumin increased the expression levels of genes related to cell death in HeLa cells 1.29- to 27.6-fold. The combination of curcumin and apigenin showed a synergistic anti-tumor effect via cross-talk between processes leading to apoptosis and autophagic cell death, as well as ER stress-associated paraptosis. GRP78 expression was down-regulated, and massive cytoplasmic vacuolization was observed in HeLa cells.

Conclusion: The combination of curcumin and apigenin is an effective potential therapeutic for cervical cancers.

Keywords: Curcumin; GRP78; HeLa cell; apigenin; apoptosis; autophagic cell death; paraptosis; synergy.

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Apigenin / pharmacology*
  • Apoptosis / drug effects*
  • Autophagic Cell Death / drug effects*
  • Caspase 3 / physiology
  • Cell Survival / drug effects
  • Curcumin / pharmacology*
  • Drug Synergism
  • Endoplasmic Reticulum Chaperone BiP
  • Female
  • HeLa Cells
  • Heat-Shock Proteins / analysis
  • Humans
  • Membrane Proteins / genetics
  • Proto-Oncogene Proteins / genetics
  • Uterine Cervical Neoplasms / drug therapy

Substances

  • Adaptor Proteins, Signal Transducing
  • BNIP3 protein, human
  • Endoplasmic Reticulum Chaperone BiP
  • HSPA5 protein, human
  • Heat-Shock Proteins
  • Membrane Proteins
  • Proto-Oncogene Proteins
  • SH3GLB1 protein, human
  • Apigenin
  • Caspase 3
  • Curcumin