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
Abstract:
Mitomycin C and cyclophosphamide are well known anti-tumor drugs. Their genotoxic effects are well established in various test systems. The genotoxic effects in non-tumor cell are of special significance due to the possibility that they may induce secondary tumors in cancer patients. Apigenin is a well known anti-oxidant and possess number of properties that are beneficial in some way to humans. With this view, the present study deals with the effect of apigenin against the genotoxic doses of mitomycin C and cyclophosphamide using chromosomal aberrations, sister chromatid exchanges and cell cycle kinetics as a parameters. The treatment of apigenin results in a significant, dose dependent decrease in the genotoxic damage, induced by mitomycin C and cyclophosphamide. It is concluded that the apigenin is potent in reducing the genotoxic damage, induced by anti-cancerous drugs, thereby reducing the chances of developing secondary tumors during the therapy.
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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