Bile Acid Concentrations, Cytotoxicity, and pH of Fecal Water from Patients with Colorectal Adenomas (original) (raw)

REFERENCES

  1. Fearon ER, Vogelstein BA: Genetic model for colorectal tumorigenesis. Cell 61:759–767, 1990
    Google Scholar
  2. Hill MJ: From adenoma to carcinoma of the colorectum. Recent Results Cancer Res 122:71–84, 1991
    Google Scholar
  3. Bruce WR: Recent hypotheses for the origin of colon cancer. Cancer Res 47:4237–4242, 1987
    Google Scholar
  4. Imray CHE, Radley S, Davis A, Barker G, Hendrickse CW, Donovan IA: Faecal unconjugated bile acids in patients with colorectal cancer or polyps. Gut 33:1239–1245, 1992
    Google Scholar
  5. De Kok TMCM, Levels PJ, Van Faassen A, Hazen M, Ten Hoor F, Kleinjans J CS: Chromatographic methods for the analysis of toxicants in feces. J Chromatogr 580:135–159, 1992
    Google Scholar
  6. Stadler J, Yeung KS, Furrer R, Marcon N, Himal HS, Bruce WR: Proliferative activity of rectal mucosa and soluble fecal bile acids in patients with normal colons and in patients with colonic polyps or cancer. Cancer Lett 38:315–320, 1988
    Google Scholar
  7. Breuer NF, D ommes P, Jaekel S, Goebell H: Fecal bile acid excretion pattern in colonic cancer patients. Dig Dis Sci 30:852–859, 1985
    Google Scholar
  8. Breuer NF, Jaekel S, Dommes P, Goebell H: Fecal bile acids in patients with adenomatous polyps of the colon. Case–control study. Digestion 34:87–92, 1986
    Google Scholar
  9. Watabe J, Bernstein H: The mutagenicity of bile acids using a fluctuation test. Mutat Res 158:45–51, 1985
    Google Scholar
  10. Wilpart M, Mainguet P, Maskens A, Roberfroid M: Mutagenicity of 1,2 dime thyl-hydrazine toward Salmon ella typh imurium, comutagenic effect of secondary bilary acids. Carcinogenesis 4:45–48, 1983
    Google Scholar
  11. Silverman SJ, Andrews AW: Bile acids: Comutagenic activity in the _Salmonella_–mammalian microsome mutagenicity test. J Natl Cancer Inst 59:1557–1559, 1977
    Google Scholar
  12. Cohen BI, Raicht FF, Deschner EE, Takahiashi M, Sarwal AM, Fazzini E: Effect of cholic acid feeding on _N_-me thyl-_N_nitrosurea induced colon tumors and cell kinetics in rats. J Natl Cancer Inst 64:573–578, 1980
    Google Scholar
  13. Martin MS, Justabo E, Jeannin JF, Leclerc A, Marin F: Effect of dietary chenodeoxycholic acid on intestinal carcinogenesis induced by 1,2-dimethylhydrazine in mice and hamsters. Br J Cancer 43:884–886, 1981
    Google Scholar
  14. Deschner EE, Raicht RF: Influence of bile on kinetic behaviours of colonic epithelial cells of the rat. Digestion 19:322–327, 1979
    Google Scholar
  15. Newmark HL, Wargovich MJ, Bruce WR: Colon cancer and dietary fat, phosphate and calcium: A hypothesis. J Natl Cancer Inst 72:1323–1325, 1984
    Google Scholar
  16. Govers MJAP, Termont DSML, Lapré JA, Kleibeuker JH, Vonk RJ, van der Meer R: Calcium in milk products precipitates intestinal fatty acids and secondary bile acids and thus inhibits colonic cytotoxicity in humans. Cancer Res 56:3270–3275, 1996
    Google Scholar
  17. De Kok TMCM, Pachen D, Baeten CGMI, Engels LGJB, ten Hoor F, Kleinjans JCS: Case–control study on fecapentaene excretion and adenomatous polyps in colon and rectum. J Natl Cancer Inst 85:1241–1244, 1993
    Google Scholar
  18. Atkin WS, Morson BC, Cuzick J: Long-term risk of colorectal cancer after excision of rectosigmoid adenomas. N Engl J Med 326:658–662, 1992
    Google Scholar
  19. Ge ltner-Allinger U, Brismar B, Reinholt FP, Andersson, Rafter JJ: Soluble fecal acidic lipids and colorectal epithelial cell proliferation in normal subjects and in patients with colon cancer. Scand J Gastroenterol 26:1069–1074, 1991
    Google Scholar
  20. van Faassen A, Hazen MJ, van den Brandt PA, van den Bogaard AE, Hermus RJJ, Janknegt RA: Bile acids and pH in total and the aqueous phase of faeces from habitual omnivores and vegetarians. Am J Clin Nutr 58:917–922, 1993
    Google Scholar
  21. Van Munster IP, Tangerman A, De Haan FJ, Nagengast FM: A new method for the determination of the cytotoxicity of bile acids and aqueous phase of stool: The effect of calcium. Eur J Clin Invest 23:773–777, 1993
    Google Scholar
  22. NEVO Table: Dutch food composition table. Bureau for Nutritional Education, The Hague 1984
  23. Owen RW, Henly PJ, Thompson MH, Hill MJ: Steroids and cancer: faecal bile acid screening for early detection of cancer risk. J Steroid Biochem 24:391–394, 1986
    Google Scholar
  24. Owen RW, Dodo M, Thompson M, Hill MJ: Faecal steroids and colorectal cancer. Nutr Cancer 9:73–80, 1987
    Google Scholar
  25. Kruis W, Forstmaier G, Scheurlen C, Stellaard F: Effect of diets low and high in refined sugars on gut transit, bile acid metabolism, and bacterial fermentation. Gut 32:367–371, 1991
    Google Scholar
  26. Geltner-Allinger U, Johansson GK, Gustafsson J, Rafter JJ: Shift from a mixed to a lactovege tarian diet: Influence on acidic lipids in fecal water—a potential risk factor for colon cancer. Am J Clin Nutr 50:992–996, 1989
    Google Scholar
  27. van Faassen A: The effect of different diets on faecal markers related to colorectal cancer risk. PhD thesis. University Maastricht, The Netherlands, 1996
    Google Scholar
  28. Lapré JA, Termont DSLM, Groen AK, Van der Meer R: Lytic effects of mixed mice lles of fatty acids and bile acids. Am J Physiol 263:G333–G337, 1992
    Google Scholar
  29. Lapré JA, De Vries HYT, Koeman HH, Van der Meer R: The antiproliferative effect of dietary calcium on colonic epithelium is mediated by luminal surfactants and dependent on the type of dietary fat. Cancer Res 53:784–789, 1993
    Google Scholar
  30. Roda A, Fini A: Effect of nuclear hydroxy substituents on aqueous solubility and acidic strength of bile acids. Hepatology 4:72S–76S, 1984
    Google Scholar
  31. van Munster IP, Tangerman A, Nagengast FM: Effect of resistant starch on colonic fermentation, bile acid metabolism and mucosal proliferation. Dig Dis Sci 39:834–842, 1994
    Google Scholar
  32. Rafter JJ, Eng VWS, Furrer R, Medline A, Bruce WR: Effects of calcium and pH on the mucosal damage produced by deoxycholic acid in the rat colon. Gut 27:1320–1329, 1986
    Google Scholar
  33. Jensen OM, Maclennan R, Wahrendorf J: Diet, bowel function, faecal characteristics and large bowel cancer in Denmark and Finland. Nutr Cancer 4:5–19, 1982
    Google Scholar
  34. Erich M, Aswell JE, van Tassell RL, Wilkins TD, Walker ARP, Richardson NJ: Mutagens in the feces of 3 South-African populations at different levels of risk for colon cancer. Mutat Res 64:231–240, 1979
    Google Scholar
  35. MacDonald IA, Webb GR, Mahony D: Fecal hydroxysteroid dehydrogenase activities in vegetarian Seventh-Day Adventists, control subjects and bowel cancer patients. Am J Clin Nutr 31:S233–S238, 1978
    Google Scholar
  36. Hove H, Rey Clausen MR, Mortensen PB: Lactate and pH in faeces from patients with colonic adenomas or cancer. Gut 34:625–629, 1993
    Google Scholar
  37. Pye G, Evans DF, Ledingham A, Hardcastle JD: Gastrointestinal intraluminal pH in normal subjects and those with colorectal adenoma or carcinoma. Gut 31:1355–1357, 1990
    Google Scholar
  38. Van der Meer R, Welberg JW, Kuipers F, Kleibeuker JH, Mulder NH, Termont DS: Effects of supplemental dietary calcium on the intestinal association of calcium, phosphate, and bile acids. Gastroenterology 99:1653–1659, 1990
    Google Scholar
  39. Gregoire RC, Stern HS, Yeung KS, Stadler J, Langley S, Furrer R: Effect of calcium supplementation on mucosal cell proliferation in high risk patients for colon cancer. Gut 30:376–382, 1989
    Google Scholar
  40. McIntyre A, Young GP, Taranto T, Gibson PR, Ward PB: Different fibers have different regional effects on luminal contents of rat colon. Gastroenterology 101:1274–1281, 1991
    Google Scholar
  41. van Munster IP, Nagengast FM: The influence of dietary fibre on bile acid metabolism. Eur J Cancer Prev 1(suppl 2):35–44, 1991
    Google Scholar

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