Skip to main content
British Journal of Cancer logoLink to British Journal of Cancer
. 1999 Jun;80(8):1132–1136. doi: 10.1038/sj.bjc.6690476

Correlation of neomycin, faecal neutral and acid sterols with colon carcinogenesis in rats

S K Panda 1, S C Chattoraj 2, S A Broitman 2
PMCID: PMC2362360  PMID: 10376962

Abstract

High fat diets have been implicated in incidence of colon cancer both in epidemiological and animal studies. Present investigation deals with the incidence, location and numbers of large and small bowel tumours induced by 1,2-dimethyl hydrazine (DMH) in rats fed high fat diets and neomycin. Neomycin was used to modify the faecal sterol metabolism and the relationship of the high fat diet and faecal neutral and acid sterols to the large bowel tumorigenesis was evaluated. DMH administered rats were fed with (a) 20% safflower oil; (b) 20% safflower oil and neomycin; (c) 20% safflower oil, cholesterol and cholic acid; and (d) 20% safflower oil, cholesterol, cholic acid and neomycin. Neomycin was found to be associated with both increase and decrease of tumour numbers. The faecal sterols lithocholic and deoxycholic acids were found to have no participation, while cholesterol and cholic acid were found to decrease with increase in tumour numbers. However, faecal coprostanol has been found to have a significant positive correlation with tumorigenesis in all dietary groups. Therefore coprostanol might possibly be associated with colon carcinogenesis in DMH-fed rats and cholesterol metabolism in gut appears to be related to the development of tumours. © 1999 Cancer Research Campaign

Keywords: safflower oil, neomycin, faecal coprostanol, colon cancer

Full Text

The Full Text of this article is available as a PDF (95.6 KB).

Selected References

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

  1. BROITMAN S. A., KINNEAR D. G., GOTTLIEB L. S., BEZMAN A. L., VITALE J. J., ZAMCHECK N. Effect of neomycin alteration of the rat intestinal flora on serum cholesterol and valvular sudanophilia. J Lab Clin Med. 1960 Jan;55:55–59. [PubMed] [Google Scholar]
  2. Broitman S. A., Vitale J. J., Vavrousek-Jakuba E., Gottlieb L. S. Polyunsaturated fat, cholesterol and large bowel tumorigenesis. Cancer. 1977 Nov;40(5 Suppl):2455–2463. doi: 10.1002/1097-0142(197711)40:5+<2455::aid-cncr2820400911>3.0.co;2-e. [DOI] [PubMed] [Google Scholar]
  3. CARPENTER K. J., GOTSIS A., HEGSTED D. M. Estimation of total cholesterol in serum by a micro method. Clin Chem. 1957 Aug;3(4 Pt 1):233–238. [PubMed] [Google Scholar]
  4. Cannizzo F., Jr, Broitman S. A. Postpromotional effects of dietary marine or safflower oils on large bowel or pulmonary implants of CT-26 in mice. Cancer Res. 1989 Aug 1;49(15):4289–4294. [PubMed] [Google Scholar]
  5. Carroll K. K. Summation: which fat/how much fat--animals. Prev Med. 1987 Jul;16(4):510–515. doi: 10.1016/0091-7435(87)90065-x. [DOI] [PubMed] [Google Scholar]
  6. Cerda S. R., Wilkinson J., 4th, Broitman S. A. Regulation of cholesterol synthesis in four colonic adenocarcinoma cell lines. Lipids. 1995 Dec;30(12):1083–1092. doi: 10.1007/BF02536608. [DOI] [PubMed] [Google Scholar]
  7. Corpet D. E., Bellier R., Petrowitsch S., Vigouroux Y. Digestion and fermentation of proteins in rats fed keratin, albumin, cooked casein and antibiotics. Reprod Nutr Dev. 1994;34(1):57–64. doi: 10.1051/rnd:19940106. [DOI] [PubMed] [Google Scholar]
  8. Deschner E. E., Winawer S. J., Long F. C., Boyle C. C. Early detection of colonic neoplasia in patients at high risk. Cancer. 1977 Nov;40(5 Suppl):2625–2631. doi: 10.1002/1097-0142(197711)40:5+<2625::aid-cncr2820400936>3.0.co;2-v. [DOI] [PubMed] [Google Scholar]
  9. Diwan B. A., Meier H., Huebner R. J. Transplacental effects of 1-ethyl-1-nitrosourea in inbred strains of mice. 3. Association between infectious or subinfectious endogenous type-C RNA tumor virus expression and chemically induced tumorigenesis. J Natl Cancer Inst. 1973 Dec;51(6):1965–1970. doi: 10.1093/jnci/51.6.1965. [DOI] [PubMed] [Google Scholar]
  10. Doll R. The geographical distribution of cancer. Br J Cancer. 1969 Mar;23(1):1–8. doi: 10.1038/bjc.1969.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Fabricant M., Broitman S. A. Evidence for deficiency of low density lipoprotein receptor on human colonic carcinoma cell lines. Cancer Res. 1990 Feb 1;50(3):632–636. [PubMed] [Google Scholar]
  12. GRUNDY S. M., AHRENS E. H., Jr, MIETTINEN T. A. QUANTITATIVE ISOLATION AND GAS--LIQUID CHROMATOGRAPHIC ANALYSIS OF TOTAL FECAL BILE ACIDS. J Lipid Res. 1965 Jul;6:397–410. [PubMed] [Google Scholar]
  13. Kesäniemi Y. A., Miettinen T. A. Inhibition of cholesterol absorption by neomycin, benzodiazepine derivatives and ketoconazole. Eur J Clin Pharmacol. 1991;40 (Suppl 1):S65–S67. [PubMed] [Google Scholar]
  14. Kraus L. J., Williams R. M., Murphy K., Broitman S. A. T-cell mitogenesis and natural killer cell activity in colonic tumor-bearing and nontumor-bearing rats fed diets high in lipid with and without cholesterol. Nutr Cancer. 1987;9(2-3):159–170. doi: 10.1080/01635588709513923. [DOI] [PubMed] [Google Scholar]
  15. Lindner M. A. A fish oil diet inhibits colon cancer in mice. Nutr Cancer. 1991;15(1):1–11. doi: 10.1080/01635589109514105. [DOI] [PubMed] [Google Scholar]
  16. MIETTINEN T. A., AHRENS E. H., Jr, GRUNDY S. M. QUANTITATIVE ISOLATION AND GAS--LIQUID CHROMATOGRAPHIC ANALYSIS OF TOTAL DIETARY AND FECAL NEUTRAL STEROIDS. J Lipid Res. 1965 Jul;6:411–424. [PubMed] [Google Scholar]
  17. Narisawa T., Fukaura Y., Yazawa K., Ishikawa C., Isoda Y., Nishizawa Y. Colon cancer prevention with a small amount of dietary perilla oil high in alpha-linolenic acid in an animal model. Cancer. 1994 Apr 15;73(8):2069–2075. doi: 10.1002/1097-0142(19940415)73:8<2069::aid-cncr2820730810>3.0.co;2-1. [DOI] [PubMed] [Google Scholar]
  18. Narisawa T., Takahashi M., Kotanagi H., Kusaka H., Yamazaki Y., Koyama H., Fukaura Y., Nishizawa Y., Kotsugai M., Isoda Y. Inhibitory effect of dietary perilla oil rich in the n-3 polyunsaturated fatty acid alpha-linolenic acid on colon carcinogenesis in rats. Jpn J Cancer Res. 1991 Oct;82(10):1089–1096. doi: 10.1111/j.1349-7006.1991.tb01762.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Ochiai M., Nakagama H., Watanabe M., Ishiguro Y., Sugimura T., Nagao M. Efficient method for rapid induction of aberrant crypt foci in rats with 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine. Jpn J Cancer Res. 1996 Oct;87(10):1029–1033. doi: 10.1111/j.1349-7006.1996.tb03105.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Raicht R. F., Cohen B. I., Shefer S., Mosbach E. H. Sterol balance studies in the rat. Effects of dietary cholesterol and beta-sitosterol on sterol balance and rate-limiting enzymes of sterol metabolism. Biochim Biophys Acta. 1975 Jun 23;388(3):374–384. doi: 10.1016/0005-2760(75)90096-x. [DOI] [PubMed] [Google Scholar]
  21. Reddy B. S. Dietary fat and colon cancer: animal model studies. Lipids. 1992 Oct;27(10):807–813. doi: 10.1007/BF02535855. [DOI] [PubMed] [Google Scholar]
  22. Reddy B. S., Martin C. W., Wynder E. L. Fecal bile acids and cholesterol metabolites of patients with ulcerative colitis, a high-risk group for development of colon cancer. Cancer Res. 1977 Jun;37(6):1697–1701. [PubMed] [Google Scholar]
  23. Sedaghat A., Samuel P., Crouse J. R., Ahrens E. H., Jr Effects of neomycin on absorption, synthesis, and/or flux of cholesterol in man. J Clin Invest. 1975 Jan;55(1):12–21. doi: 10.1172/JCI107902. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Steiner A., Weisser B., Vetter W. A comparative review of the adverse effects of treatments for hyperlipidaemia. Drug Saf. 1991 Mar-Apr;6(2):118–130. doi: 10.2165/00002018-199106020-00003. [DOI] [PubMed] [Google Scholar]
  25. Wynder E. L. The epidemiology of large bowel cancer. Cancer Res. 1975 Nov;35(11 Pt 2):3388–3394. [PubMed] [Google Scholar]

Articles from British Journal of Cancer are provided here courtesy of Cancer Research UK

RESOURCES