ISPO

Published in Cancer Detection and Prevention 2001; 25(4):362-368.

Inhibitory Effects of Thymoquinone against 20-Methyicholanthrene-Induced Fibrosarcoma Tumorigenesis

Osama A. Badary, PhD,a and Ayman M. Gamal El-Din, PhDb

Departments of aPharmacology and Toxicology and bBiochemistry, College of Pharmacy, AI-Azhar University, Cairo, Egypt

Address all correspondence and reprint requests to: Osama A. Badary, PhD, Department of Pharmacology and Toxicology, College of Pharmacy. AI-Azhar University, Nasr City, Cairo, Egypt.

ABSTRACT: The potential antitumor effect of thymoquinone (TQ), the main constituent of the volatile oil of Nigella sativa seed, on fibrosarcoma induced by 20-methylcholanthrene (MC) in male Swiss albino mice was investigated in vivo and in vitro. Administration of TQ (0.01% in drinking water) I week before and after MC treatment significantly inhibited the tumor incidence and tumor burden by 43% and 34%, respectively, compared with the results in the group receiving MC alone. Moreover, TQ delayed the onset of MC-induced fibrosarcoma tumors that appeared at 12 weeks and produced less MC-induced mortality. Lipid peroxide accumulation, decreased glutathione (GSH) content, and decreased activities of glutathione 5-transferase (GST) and quinone reductase (QR) were observed in the liver of MC-induced tumor-bearing mice. TQ alone showed a significant induction in the enzyme activities of hepatic GST and QR. Mice treated with TQ along with MC showed reduction in hepatic lipid peroxides and increased GSH content and increased enzyme activities of GST and QR as compared to results of the control group. The in vitro studies showed that TQ inhibited the survival of fibrosarcoma cells with IC50 of 15 muM. Conversely, TQ inhibited the incorporation of [3H] thymidine in fibrosarcoma cells with IC51 of I muM. Our data indicate the potential of TQ as a powerful chemopreventive agent against MC-induced fibrosarcoma tumors. The possible modes of action of TQ may be through its antioxidant activity and interference with the DNA synthesis coupled with enhancement of detoxification processes.

KEY WORDS: chemoprevention, detoxification, DNA synthesis, methylcholanthrene.

http://www.cancerprev.org/Journal/Issues/25/4/3861