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Carcinogenesis Advance Access published online on December 7, 2005

Carcinogenesis, doi:10.1093/carcin/bgi286
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© The Author 2005. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org
Received May 17, 2005
Revised November 6, 2005
Accepted November 22, 2005

MOLECULAR EPIDEMIOLOGY AND CANCER PREVENTION

Chemopreventive effect of trans-resveratrol - a phytoalexin against colonic aberrant crypt foci and cell proliferation in 1,2-dimethylhydrazine induced colon carcinogenesis

Murugan Sengottuvelan 1, Periaswamy Viswanathan 2, and Namasivayam Nalini 1 *

1 Department of Biochemistry and Biotechnology, Faculty of Science, Rajah Muthiah Medical College, Annamalai University, Annamalainagar - 608 002, Tamilnadu, India
2 Department of Pathology, Faculty of Medicine, Rajah Muthiah Medical College, Annamalai University, Annamalainagar - 608 002, Tamilnadu, India

* To whom correspondence should be addressed.
Namasivayam Nalini, E-mail: nalininam{at}yahoo.com


   Abstract

Prevention of cancer remains a primary need and new chemopreventive agents must be developed for this purpose. Towards this goal, a chemoprevention study was conducted to evaluate the activity of resveratrol (Res), a phytoalexin, as an inhibitor of colon carcinogenesis. Wistar male rats were divided into six groups, group 1 were control rats, group 2 were control rats that received Res (8 mg/kg body weight p.o. everyday), rats in groups 3-6 were treated weekly with 1,2-dimethylhydrazine (DMH, 20 mg/kg body weight, s.c. x 15 times). In addition, groups 4, 5 and 6 received Res as in group 2. Modifying effects were assessed using aberrant crypt foci (ACF) and the extent of histopathological lesions as end point markers. At the end of 30 weeks, Res markedly reduced tumor incidence, the degree of histological lesions and also the size of tumors significantly (P < 0.05) as compared to the unsupplemented DMH-treated rats. The number of ACF consisting of more than six aberrant crypts per rat was observed in group 6 (6.2 ± 1.4), group 5 (7.7 ± 1.0) and group 4 (8.2 ± 1.4) which were significantly lower than that of group 3 (22.3 ± 2.4) (P < 0.05). The most pronounced inhibition of ACF development was noted in rats fed Res for the entire period and also during the post-initiation period. Also, Res administration lowered the number of argyrophilic nucleolar organizing region-associated proteins (AgNORs) per nucleus in non-lesional colonic crypts, which reflects the cell proliferation activity. Oxidative imbalance in DMH-treatment was significantly (P < 0.01) modulated on Res supplementation as indicated by optimal concentration of thiobarbituric acid reactive substances (TBARS), superoxide dismutase (SOD), catalase (CAT), and reduced glutathione (GSH). The results of our study suggest Res as an effective chemopreventive agent, which suppresses DMH-induced colon carcinogenesis at various stages.

Keywords: aberrant crypt foci; antioxidants; chemoprevention; colon cancer; 1,2-dimethylhydrazine; lipid peroxidation; resveratrol.
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