Antigenotoxic effect of apigenin against anti-cancerous drugs

Yasir Hasan Siddique1, Tanveer Beg, Mohammad Afzal

  • 1Human Genetics and Toxicology Lab, Section of Genetics, Department of Zoology, Faculty of Life Sciences, Aligarh Muslim University, Aligarh, U.P. 202002, India. yasir_hasansiddique@rediffmail.com

Insights

Apigenin significantly reduces genotoxic damage caused by anti-tumor drugs Mitomycin C and cyclophosphamide. This antioxidant may help prevent secondary tumors in cancer patients undergoing chemotherapy.

Area of Science:

  • Pharmacology
  • Toxicology
  • Oncology

Background:

  • Mitomycin C and cyclophosphamide are established anti-tumor drugs with known genotoxic effects.
  • Genotoxicity in non-tumor cells is a concern due to the risk of secondary tumor induction in cancer patients.
  • Apigenin is recognized for its antioxidant properties and potential health benefits.

Purpose of the Study:

  • To investigate the protective effects of apigenin against the genotoxicity induced by Mitomycin C and cyclophosphamide.
  • To evaluate apigenin's efficacy in mitigating DNA damage and chromosomal abnormalities.
  • To assess apigenin's impact on cell cycle kinetics in the presence of genotoxic agents.

Main Methods:

  • Chromosomal aberration analysis
  • Sister chromatid exchange assays
  • Cell cycle kinetics studies
  • Dose-dependent treatment with apigenin, Mitomycin C, and cyclophosphamide

Main Results:

  • Apigenin treatment demonstrated a significant, dose-dependent reduction in genotoxic damage.
  • Mitomycin C and cyclophosphamide induced chromosomal aberrations and cell cycle disturbances.
  • Apigenin mitigated these genotoxic effects, showing protective activity.

Conclusions:

  • Apigenin exhibits potent chemopreventive properties against genotoxicity induced by common anti-cancer drugs.
  • The findings suggest apigenin can reduce the risk of secondary malignancies associated with chemotherapy.
  • Apigenin represents a potential therapeutic adjunct for cancer patients to minimize drug-induced genotoxic side effects.

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