Gemini Curcumin Suppresses Proliferation of Ovarian Cancer OVCAR-3 Cells via Induction of Apoptosis

Anticancer Agents Med Chem. 2021;21(6):775-781. doi: 10.2174/1871520620666200807223340.

Abstract

Background: Ovarian cancer has the highest mortality rate among gynecological malignancies. Despite recent advances in treatment, most patients still suffer from poor prognosis. Curcumin has shown highly cytotoxic effects against different types of cancer. However, its poor bioavailability restricts its clinical application. Gemini Curcumin (Gemini-Cur) has been developed to overcome this limitation.

Objective: Here, we aimed to unravel the inhibitory effect of Gemini-Cur in ovarian cancer.

Methods: OVCAR-3 cells were treated with free curcumin and Gemni-Cur in a time- and dose-dependent manner. Then, the anticancer activity was investigated by uptake kinetics, cellular viability and apoptotic assays. Furthermore, we evaluated the BAX/Bcl-2 expression ratio by real-time PCR and western blotting.

Results: Our data showed that gemini surfactant nanoparticles enhance the cellular uptake of curcumin compared to free curcumin (p<0.01). Regarding the growth inhibitory effect of nano-curcumin, the results demonstrated that Gemini-Cur suppresses the proliferation of OVCAR-3 cells through induction of apoptosis (p<0.001).

Conclusion: The results illustrate that Gemini-Cur nanoparticles have a great potential for developing novel therapeutics against ovarian cancer.

Keywords: BAX/Bcl-2; Curcumin; OVCAR-3; apoptosis; gemini surfactant; ovarian cancer.

MeSH terms

  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / pharmacology
  • Apoptosis / drug effects
  • Biological Transport
  • Calcitriol / analogs & derivatives*
  • Calcitriol / chemistry
  • Carcinoma, Ovarian Epithelial / drug therapy*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Curcumin / chemistry*
  • Curcumin / pharmacology
  • Drug Compounding
  • Drug Liberation
  • Female
  • Humans
  • Nanocapsules / chemistry*
  • Ovarian Neoplasms / drug therapy*
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Signal Transduction
  • bcl-2-Associated X Protein / drug effects
  • bcl-2-Associated X Protein / metabolism

Substances

  • 1,25-dihydroxy-21-(3-hydroxy-3-methylbutyl)vitamin D(3)
  • Antineoplastic Agents
  • Nanocapsules
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein
  • Calcitriol
  • Curcumin