Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (65)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Anisimov, V. N.
Right arrow Articles by Zabezhinski, M. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Anisimov, V. N.
Right arrow Articles by Zabezhinski, M. A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Carcinogenesis, Vol 18, 1549-1553, Copyright © 1997 by Oxford University Press


ARTICLES

Melatonin and colon carcinogenesis: I. Inhibitory effect of melatonin on development of intestinal tumors induced by 1,2-dimethylhydrazine in rats

VN Anisimov, IG Popovich and MA Zabezhinski
Laboratory of Experimental Tumors, N.N. Petrov Research Institute of Oncology, St Petersburg, Russia.

The effect of pineal indole hormone melatonin on colon carcinogenesis was firstly studied in rats. Two-month-old outbred female LIO rats were weekly exposed to 15 (experiment 1, groups 1 and 2) or to five (experiment 2, groups 1 and 2) s.c. injections of 1,2-dimethylhydrazine (DMH) at a single dose of 21 mg/kg of body weight. From the day of the first injection of the carcinogen DMH, the rats from groups 2 (experiments 1 and 2) were given melatonin five days a week during the night-time (from 18:00 h to 8:00 h), dissolved in tap water at 20 mg/l. The experiment was finalized in 6 months after the first injection of DMH. In both experiments the majority of tumors were localized in the descending colon. Tumors of the small intestines developed only in rats from experiment 1. Total incidence of colon tumors as well as tumors in different parts of the colon and the mean number of tumors per rat were much higher in rats from both groups in experiment 1 than that in rats from experiment 2. In experiment 1 melatonin failed to influence the total incidence of colon tumors. However, incidence of carcinomas in the ascending colon was significantly reduced (P < 0.01). The multiplicity of total colon tumors per rat, as well as the mean number of tumors, ascending and descending colon per rat, was also decreased under the influence of melatonin (group 2 vs group 1, P < 0.01). In the same experiment, melatonin slightly decreased the depth of tumor invasion and increased number of highly differentiated colon carcinomas induced by DMH. The percentage of small tumours in the descending colon among rats from group 2 was higher than that of group 1. Treatment with melatonin was also followed by a decrease in the multiplicity of DMH- induced tumors of the duodenum (group 2 vs group 1, P < 0.05) and by a decrease in the incidence of jejunum and ileum tumors (group 2 vs group 1, P < 0.05). In experiment 2, the inhibitory effect of melatonin on DMH-induced colon carcinogenesis was much more expressed than that in experiment 1. Thus, in group 1 the incidence of total colon tumors, ascending and descending colon tumors, was significantly decreased in comparison with group 2; also melatonin reduced the number of tumors per rat in the ascending and descending colon. The number of colon tumors that invaded only mucosa was significantly higher in group 2 than in group 1, P < 0.05. The ratio of highly differentiated tumors was increased (P < 0.05) and the ratio of low-differentiated tumors was decreased (P < 0.05) in rats exposed to melatonin (group 4) as compared with group 3. The number of large size tumors in the ascending and descending colon was decreased whereas the number of small size tumors (<10 mm2) was increased in those parts of the colon that were under the influence of melatonin in experiment 2. Thus, our results demonstrate the inhibitory effect of melatonin on intestinal carcinogenesis induced by DMH in rats.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Cancer Epidemiol. Biomarkers Prev.Home page
D. K. Mirick and S. Davis
Melatonin as a Biomarker of Circadian Dysregulation
Cancer Epidemiol. Biomarkers Prev., December 1, 2008; 17(12): 3306 - 3313.
[Abstract] [Full Text] [PDF]


Home page
Toxicol PatholHome page
V. N. Anisimov
Effects of Exogenous Melatonin--A Review
Toxicol Pathol, October 1, 2003; 31(6): 589 - 603.
[Abstract] [PDF]


Home page
JNCI J Natl Cancer InstHome page
E. S. Schernhammer, F. Laden, F. E. Speizer, W. C. Willett, D. J. Hunter, I. Kawachi, C. S. Fuchs, and G. A. Colditz
Night-Shift Work and Risk of Colorectal Cancer in the Nurses' Health Study
J Natl Cancer Inst, June 4, 2003; 95(11): 825 - 828.
[Abstract] [Full Text] [PDF]


Home page
JCOHome page
Vijayalaxmi, C. R. Thomas Jr, R. J. Reiter, and T. S. Herman
Melatonin: From Basic Research to Cancer Treatment Clinics
J. Clin. Oncol., May 15, 2002; 20(10): 2575 - 2601.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
K. Imaida, K. Kuzutani, J. Wang, O. Fujiwara, T. Ogiso, K. Kato, and T. Shirai
Lack of promotion of 7,12-dimethylbenz[a]anthracene-initiated mouse skin carcinogenesis by 1.5 GHz electromagnetic near fields
Carcinogenesis, November 1, 2001; 22(11): 1837 - 1841.
[Abstract] [Full Text] [PDF]


Home page
JNCI J Natl Cancer InstHome page
E. S. Schernhammer, F. Laden, F. E. Speizer, W. C. Willett, D. J. Hunter, I. Kawachi, and G. A. Colditz
Rotating Night Shifts and Risk of Breast Cancer in Women Participating in the Nurses' Health Study
J Natl Cancer Inst, October 17, 2001; 93(20): 1563 - 1568.
[Abstract] [Full Text] [PDF]


Home page
Journals of Gerontology Series A: Biological Sciences and Medical SciencesHome page
V. N. Anisimov, N. Y. Zavarzina, M. A. Zabezhinski, I. G. Popovich, O. A. Zimina, A. V. Shtylick, A. V. Arutjunyan, T. I. Oparina, V. M. Prokopenko, A. I. Mikhalski, et al.
Melatonin Increases Both Life Span and Tumor Incidence in Female CBA Mice
J. Gerontol. A Biol. Sci. Med. Sci., July 1, 2001; 56(7): B311 - 323.
[Abstract] [Full Text] [PDF]


Home page
International Journal of ToxicologyHome page
A. C. Maritim, B. H. Moore, R. A. Sanders, and J. B. Watkins III
Effect of Melatonin on Phase I and II Biotransformation Enzymes in Streptozotocin-Induced Diabetic Rats
International Journal of Toxicology, July 1, 2000; 19(4): 277 - 283.
[Abstract] [PDF]


Home page
International Journal of ToxicologyHome page
A. C. Maritim, B. H. Moore, R. A. Sanders, and J. B. Watkins III
Effects of Melatonin on Oxidative Stress in Streptozotocin-Induced Diabetic Rats
International Journal of Toxicology, April 1, 1999; 18(3): 161 - 166.
[Abstract] [PDF]


Home page
MutagenesisHome page
R. De Salvia, M. Fiore, T. Aglitti, F. Festa, R. Ricordy, and R. Cozzi
Inhibitory action of melatonin on H2O2- and cyclophosphamide-induced DNA damage
Mutagenesis, January 1, 1999; 14(1): 107 - 112.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.