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British Journal of Experimental Pathology logoLink to British Journal of Experimental Pathology
. 1988 Feb;69(1):149–154.

The relationship between faecal bile acids and the development of experimental colon cancer.

T Barton 1, J P Cruse 1, M R Lewin 1
PMCID: PMC2013201  PMID: 3348957

Abstract

Human metabolic studies have suggested a positive association between dietary intake, faecal bile acid excretion and the development of colon cancer. Similar investigations in experimental models of this disease have also implicated faecal bile acids but in both animals and man the results remain equivocal. This study sequentially examines the outputs and concentrations of faecal bile acids in dimethylhydrazine (DMH) treated groups of rats (n = 10), killed at 5-weekly intervals from the 10th to 40th week following the first injection. The sequential results showed that both the output and concentration of faecal bile acids decreased with time and accompanied an increase in both the incidence and numbers of colonic neoplasms over the 40 weeks of the study. When the animals were grouped according to the histological classification of their tumours, the faecal bile acids did not differ between animals with and without tumours. Further, when the latter group were sub-divided into those with adenomas alone and those with carcinomas, faecal bile acid outputs and concentrations did not differ between them, nor when they were compared with the tumour-free animals. The results of this study do not support a role for faecal bile acids in the dimethylhydrazine-induced model of experimental colon cancer in rats.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Boutwell R. K. The function and mechanism of promoters of carcinogenesis. CRC Crit Rev Toxicol. 1974 Jan;2(4):419–443. doi: 10.3109/10408447309025704. [DOI] [PubMed] [Google Scholar]
  2. Breuer N. F., Dommes P., Jaekel S., Goebell H. Fecal bile acid excretion pattern in colonic cancer patients. Dig Dis Sci. 1985 Sep;30(9):852–859. doi: 10.1007/BF01309516. [DOI] [PubMed] [Google Scholar]
  3. Cohen B. I., Raicht R. F., Deschner E. E., Takahashi M., Sarwal A. N., Fazzini E. Effect of cholic acid feeding on N-methyl-N-nitrosourea-induced colon tumors and cell kinetics in rats. J Natl Cancer Inst. 1980 Mar;64(3):573–578. [PubMed] [Google Scholar]
  4. Cruse J. P., Lewin M. R., Clark C. G. The effects of cholic acid and bile salt binding agents on 1,2-dimethylhydrazine-induced colon carcinogenesis in the rat. Carcinogenesis. 1981;2(5):439–443. doi: 10.1093/carcin/2.5.439. [DOI] [PubMed] [Google Scholar]
  5. Cruse J. P., Lewin M. R., Ferulano G. P., Clark C. G. Experimental evidence against the bile salt theory of colon carcinogenesis. Eur Surg Res. 1981;13(2):117–124. doi: 10.1159/000128177. [DOI] [PubMed] [Google Scholar]
  6. Gilbert J. M., Setchell K. D., Lawson A. M., Royston J. P., Worthington J., Kark A. Detailed faecal bile acid profile: a diagnostic test for colorectal cancer? Eur J Surg Oncol. 1986 Dec;12(4):359–365. [PubMed] [Google Scholar]
  7. Hill M. J., Drasar B. S., Williams R. E., Meade T. W., Cox A. G., Simpson J. E., Morson B. C. Faecal bile-acids and clostridia in patients with cancer of the large bowel. Lancet. 1975 Mar 8;1(7906):535–539. doi: 10.1016/s0140-6736(75)91556-1. [DOI] [PubMed] [Google Scholar]
  8. Hill M. J. The etiology of colon cancer. CRC Crit Rev Toxicol. 1975 Oct;4(1):31–82. doi: 10.1080/10408447509163834. [DOI] [PubMed] [Google Scholar]
  9. Martin M. S., Justrabo E., Jeannin J. F., Leclerc A., Martin F. Effect of dietary chenodeoxycholic acid on intestinal carcinogenesis induced by 1.2 dimethylhydrazine in mice and hamsters. Br J Cancer. 1981 Jun;43(6):884–886. doi: 10.1038/bjc.1981.130. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Mower H. F., Ray R. M., Shoff R., Stemmermann G. N., Nomura A., Glober G. A., Kamiyama S., Shimada A., Yamakawa H. Fecal bile acids in two Japanese populations with different colon cancer risks. Cancer Res. 1979 Feb;39(2 Pt 1):328–331. [PubMed] [Google Scholar]
  11. Mudd D. G., McKelvey S. T., Norwood W., Elmore D. T., Roy A. D. Faecal bile acid concentration of patients with carcinoma or increased risk of carcinoma in the large bowel. Gut. 1980 Jul;21(7):587–590. doi: 10.1136/gut.21.7.587. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Murray W. R., Backwood A., Trotter J. M., Calman K. C., MacKay C. Faecal bile acids and clostridia in the aetiology of colorectal cancer. Br J Cancer. 1980 Jun;41(6):923–928. doi: 10.1038/bjc.1980.170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Narisawa T., Magadia N. E., Weisburger J. H., Wynder E. L. Promoting effect of bile acids on colon carcinogenesis after intrarectal instillation of N-methyl-N'-nitro-N-nitrosoguanidine in rats. J Natl Cancer Inst. 1974 Oct;53(4):1093–1097. doi: 10.1093/jnci/53.4.1093. [DOI] [PubMed] [Google Scholar]
  14. Reddy B. S., Mastromarino A., Gustafson C., Lipkin M., Wynder E. L. Fecal bile acids and neutral sterols in patients with familial polyposis. Cancer. 1976 Oct;38(4):1694–1698. doi: 10.1002/1097-0142(197610)38:4<1694::aid-cncr2820380442>3.0.co;2-m. [DOI] [PubMed] [Google Scholar]
  15. Reddy B. S., Watanabe K., Weisburger J. H., Wynder E. L. Promoting effect of bile acids in colon carcinogenesis in germ-free and conventional F344 rats. Cancer Res. 1977 Sep;37(9):3238–3242. [PubMed] [Google Scholar]

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