Cancer Research Infection and Cancer: Biology, Therapeutics, and Prevention  Tumor Immunology: New Perspectives
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 39, 1207-1217, April 1, 1979]
© 1979 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cohen, S. M.
Right arrow Articles by Friedell, G. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cohen, S. M.
Right arrow Articles by Friedell, G. H.

Promoting Effect of Saccharin and DL-Tryptophan in Urinary Bladder Carcinogenesis1

Samuel M. Cohen2, Masayuki Aral3, Jerome B. Jacobs and Gilbert H. Friedell

Department of Pathology, St. Vincent Hospital, and Department of Pathology, the University of Massachusetts Medical School, Worcester, Massachusetts 01604

The existence of at least two stages in bladder carcinogenesis was evaluated in male Fischer rats using N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide (FANFT) fed for six weeks at a level of 0.2% of the diet as the initiator. Sodium saccharin and DL-tryptophan were fed at levels of 5 and 2% of the diet, respectively, as possible promoting chemicals, and they were fed either immediately after FANFT administration or after six weeks of FANFT plus six weeks of control diet. All surviving rats were killed at the end of two years. Both chemicals significantly increased the incidence of bladder tumors following FANFT feeding compared to six weeks of FANFT feeding followed by control diet, and the results were similar whether saccharin or tryptophan feeding was started immediately after FANFT feeding was concluded or after a six-week delay. Saccharin was considerably more potent as a promoting agent than was tryptophan, inducing higher incidences of bladder tumors and having a shorter latent period. Long-term administration of FANFT induced a 100% incidence of bladder cancer. Sequential epithelial changes were observed by scanning and transmission electron microscopy as well as by light microscopy. Pleomorphic microvilli were present on the superficial cells of all tumors examined and on the surface cells of hyperplastic bladder epithelium after six weeks of FANFT plus six weeks of saccharin, but not after six weeks of FANFT and six weeks of control diet. Rats fed only saccharin, tryptophan, or control diet did not have bladder tumors or pleomorphic microvilli on bladder epithelium. These data suggest that saccharin and tryptophan might act as tumor-promoting agents during bladder carcinogenesis.

1 Supported in part by USPHS Grant CA15495 from the National Cancer Institute through the National Bladder Cancer Project. A preliminary report of this work was presented (19).

2 To whom requests for reprints should be addressed, at Department of Pathology, St. Vincent Hospital, Worcester, Mass. 01604.

3 Present address: First Department of Pathology, Nagoya City University Medical School, Nagoya 467, Japan.

Received 10/ 5/78. Accepted 12/22/78.




This article has been cited by other articles:


Home page
CarcinogenesisHome page
S. M. Cohen, L. L. Arnold, M. Cano, M. Ito, E. M. Garland, and R.A. Shaw
Calcium phosphate-containing precipitate and the carcinogenicity of sodium salts in rats
Carcinogenesis, April 1, 2000; 21(4): 783 - 792.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
C. C. R. Lee, T. Ichihara, S. Yamamoto, H. Wanibuchi, K. Sugimura, S. Wada, T. Kishimoto, and S. Fukushima
Reduced expression of the CDK inhibitor p27KIP1 in rat two-stage bladder carcinogenesis and its association with expression profiles of p21WAF1/Cip1 and p53
Carcinogenesis, September 1, 1999; 20(9): 1697 - 1708.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
K. Morimura, S. Yamamoto, T. Murai, S. Mori, T.-X. Chen, H. Wanibuchi, and S. Fukushima
LOH and mutational analysis of p53 alleles in mouse urinary bladder carcinomas induced by N-butyl-N-(4-hydroxybutyl) nitrosamine
Carcinogenesis, April 1, 1999; 20(4): 715 - 718.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
Y Nishio, T Kakizoe, M Ohtani, S Sato, T Sugimura, and S Fukushima
L-isoleucine and L-leucine: tumor promoters of bladder cancer in rats
Science, February 21, 1986; 231(4740): 843 - 845.
[Abstract] [PDF]


Home page
ScienceHome page
E. Wynder and S. Stellman
Artificial sweetener use and bladder cancer: a case-control study
Science, March 14, 1980; 207(4436): 1214 - 1216.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1979 by the American Association for Cancer Research.