Skip to main content
Erschienen in: European Journal of Nutrition 6/2008

01.09.2008 | ORIGINAL CONTRIBUTION

Genotoxic effect of bile acids on human normal and tumour colon cells and protection by dietary antioxidants and butyrate

verfasst von: Patrizia Rosignoli, Roberto Fabiani, Angelo De Bartolomeo, Raffaela Fuccelli, Maria Antonietta Pelli, Guido Morozzi

Erschienen in: European Journal of Nutrition | Ausgabe 6/2008

Einloggen, um Zugang zu erhalten

Abstract

Background

Colorectal cancer is the second cause of death for tumour worldwide. Among the risk factors for this disease the dietary habits seem to have a pivotal role. An elevated intake of fats causes a high release in the gut lumen of bile acids that are positively correlated with colorectal cancer, since they act as detergents and proliferation promoters. Recently, it was evidenced that bile acids can also be able to induce DNA damage.

Aim of the study

In this study the genotoxicity of deoxycholic acid (DCA) and chenodeoxycholic acid CDCA) has been evaluated in human normal colonocytes derived from 60 colon biopsies and in tumour cells. The involvement of reactive oxygen species (ROS) and the oxidative DNA damage was assessed. In addition, the protective effect exerted by both two well-known antioxidants commonly present in the diet, β-carotene and α-tocopherol, and butyrate which is known to be involved in the regulation of several cellular functions, has also been tested.

Methods

The DNA damage was evaluated by the “comet assay” or single cell gel electrophoresis (SCGE) both in its conventional use and by the Endonuclease III modified method, which allow to detect the presence of oxidized pyrimidines.

Results

Bile acids (CDA and CDCA) resulted genotoxic on both normal and tumour human colon cells. The inclusion of the endonuclease III digestion step in the comet assay demonstrated that bile acids induced an oxidative DNA damage. In addition, treatment of colonocytes with bile acids in the presence of the antioxidants (β-carotene, α-tocopherol) and Na-butyrate caused a reduction of DNA damage.

Conclusion

Our results suggest that bile acids may be involved in the tumour initiation by inducing a DNA oxidative damage, and so add further evidences to the preventive properties of antioxidants present in the Mediterranean diet.
Literatur
1.
Zurück zum Zitat Bartram HP, Scheppach W, Englert S, Dusel G, Richter A, Richter F, Kasper H (1995) Effects of deoxycholic acid and butyrate on mucosal prostaglandin E2 release and cell proliferation in the human sigmoid colon. J Parenter Enteral Nutr 19:182–186CrossRef Bartram HP, Scheppach W, Englert S, Dusel G, Richter A, Richter F, Kasper H (1995) Effects of deoxycholic acid and butyrate on mucosal prostaglandin E2 release and cell proliferation in the human sigmoid colon. J Parenter Enteral Nutr 19:182–186CrossRef
2.
Zurück zum Zitat Bernestein H, Payne CM, Bernestein C, Schneider J, Beard SE, Crowley CL (1999) Activation of the promoters of genes associated with DNA damage, oxidative stress, ER stress and protein malfonding by the bile salt, deoxycholate. Toxicol Lett 108:37–46CrossRef Bernestein H, Payne CM, Bernestein C, Schneider J, Beard SE, Crowley CL (1999) Activation of the promoters of genes associated with DNA damage, oxidative stress, ER stress and protein malfonding by the bile salt, deoxycholate. Toxicol Lett 108:37–46CrossRef
3.
Zurück zum Zitat Bernstein H, Bernstein C, Payne CM, Dvorakova K, Garewal H (2005) Bile acids as carcinogens in human gastrointestinal cancers. Mutat Res 589:47–65CrossRef Bernstein H, Bernstein C, Payne CM, Dvorakova K, Garewal H (2005) Bile acids as carcinogens in human gastrointestinal cancers. Mutat Res 589:47–65CrossRef
4.
Zurück zum Zitat Booth LA, Gilmore IT, Bilton RF (1997) Secondary bile acid induced DNA damage in HT29 cells: are free radicals involved? Free Rad Res 26:135–144CrossRef Booth LA, Gilmore IT, Bilton RF (1997) Secondary bile acid induced DNA damage in HT29 cells: are free radicals involved? Free Rad Res 26:135–144CrossRef
5.
Zurück zum Zitat Booth LA, Gilmore IT, Bilton RF (1997) Secondary bile acid induced DNA damage in HT29 cells: are free radicals involved? Free Rad Res 26:135–144CrossRef Booth LA, Gilmore IT, Bilton RF (1997) Secondary bile acid induced DNA damage in HT29 cells: are free radicals involved? Free Rad Res 26:135–144CrossRef
6.
Zurück zum Zitat Collins AR, Duthie SJ, Dobson VL (1993) Direct enzyme detection of endogenous oxidative base damage in human lymphocytes DNA. Carcinogenesis 14:1733–1735CrossRef Collins AR, Duthie SJ, Dobson VL (1993) Direct enzyme detection of endogenous oxidative base damage in human lymphocytes DNA. Carcinogenesis 14:1733–1735CrossRef
7.
Zurück zum Zitat Crowley-Weber CL, Dvorakova K, Crowley C, Bernstein H, Bernstein C, Garewal H, Payne MC (2003) Nicotine increases oxidative stress, activates NF-kB and GRP78, induces apoptosis and sensitizes cells to genotoxic/xenobiotic stresses by a multiple stress inducer, deoxycholate:relevance to colon carcinogenesis. Chem Biol Inter 145:53–66CrossRef Crowley-Weber CL, Dvorakova K, Crowley C, Bernstein H, Bernstein C, Garewal H, Payne MC (2003) Nicotine increases oxidative stress, activates NF-kB and GRP78, induces apoptosis and sensitizes cells to genotoxic/xenobiotic stresses by a multiple stress inducer, deoxycholate:relevance to colon carcinogenesis. Chem Biol Inter 145:53–66CrossRef
8.
Zurück zum Zitat D’Argenio G, Mazzacca G (1999) Short chain fatty acids in the human colon. Relation to inflammatory bowel diseases and colon cancer. Adv Exp Med Biol 472:149–158 D’Argenio G, Mazzacca G (1999) Short chain fatty acids in the human colon. Relation to inflammatory bowel diseases and colon cancer. Adv Exp Med Biol 472:149–158
9.
Zurück zum Zitat Davidovic M (1999) Genetic stability: the key to longevity? Med Hypoth 53:329–332CrossRef Davidovic M (1999) Genetic stability: the key to longevity? Med Hypoth 53:329–332CrossRef
10.
Zurück zum Zitat Deschner EE, Cohen BI, Raicht RF (1981) Acute and chronic effect of dietary cholic acid on colonic epithelial cell proliferation. Digestion 21:290–296 Deschner EE, Cohen BI, Raicht RF (1981) Acute and chronic effect of dietary cholic acid on colonic epithelial cell proliferation. Digestion 21:290–296
11.
Zurück zum Zitat Fabiani R, De Bartolomeo A, Rosignoli P, Servili M, Montedoro GF, Morozzi G (2002) Cancer chemioprevention by hydroxytyrosol isolated from virgin olive oil through G1 cell cycle arrest and apoptosis. Eur J Cancer Prev 11:351–358CrossRef Fabiani R, De Bartolomeo A, Rosignoli P, Servili M, Montedoro GF, Morozzi G (2002) Cancer chemioprevention by hydroxytyrosol isolated from virgin olive oil through G1 cell cycle arrest and apoptosis. Eur J Cancer Prev 11:351–358CrossRef
12.
Zurück zum Zitat Glinghammar B, Inoue H, Rafter JJ (2002) Deoxycholic acid causes DNA damage in colonic cells with subsequent induction of capsases, COX-2 promoter activity and the trascription factors NF.kB and AP-1. Carcinogenesis 23:839–845CrossRef Glinghammar B, Inoue H, Rafter JJ (2002) Deoxycholic acid causes DNA damage in colonic cells with subsequent induction of capsases, COX-2 promoter activity and the trascription factors NF.kB and AP-1. Carcinogenesis 23:839–845CrossRef
13.
Zurück zum Zitat Grossmann J, Walther K, Artinger M, Kiessling S, Scholmerich J (2001) Apoptotic signaling during initiation of detachment-induced apoptosis (“Anoikis”) of primary human intestinal epithelial cells. Cell Growth Differ 12:147–155 Grossmann J, Walther K, Artinger M, Kiessling S, Scholmerich J (2001) Apoptotic signaling during initiation of detachment-induced apoptosis (“Anoikis”) of primary human intestinal epithelial cells. Cell Growth Differ 12:147–155
14.
Zurück zum Zitat Hamada K, Umemoto A, Kajikawa A, Seraj MJ, Monden Y (1994) In vitro formation of DNA adducts with bile acids. Carcinogenesis 15:1911–1915CrossRef Hamada K, Umemoto A, Kajikawa A, Seraj MJ, Monden Y (1994) In vitro formation of DNA adducts with bile acids. Carcinogenesis 15:1911–1915CrossRef
15.
Zurück zum Zitat Hartmann A, Speit G (1997) The contribution of cytotoxicity to DNA-effects in the single cell gel test (comet assay). Toxicol Lett 90:183–188CrossRef Hartmann A, Speit G (1997) The contribution of cytotoxicity to DNA-effects in the single cell gel test (comet assay). Toxicol Lett 90:183–188CrossRef
16.
Zurück zum Zitat Haza AI, Glinghammar B, Grandine A, Rafter J (2000) Effect of colonic luminal components on induction of apoptosis in human colonic cell lines. Nutr Cancer 36:79–89CrossRef Haza AI, Glinghammar B, Grandine A, Rafter J (2000) Effect of colonic luminal components on induction of apoptosis in human colonic cell lines. Nutr Cancer 36:79–89CrossRef
17.
Zurück zum Zitat Huang XP, Fan XT, Desjeux JF, Castagna M (1992) Bile acids, non-phorbol-ester-type tumor promoters, stimulate the phosphorilation of protein kinase C substrates in human platelets and colon cell line HT 29. Int J Cancer 52:444–450CrossRef Huang XP, Fan XT, Desjeux JF, Castagna M (1992) Bile acids, non-phorbol-ester-type tumor promoters, stimulate the phosphorilation of protein kinase C substrates in human platelets and colon cell line HT 29. Int J Cancer 52:444–450CrossRef
18.
Zurück zum Zitat Janson W, Brandner G, Siegel J (1997) Butyrate modulates DNA damage-induced p53 response by induction of p53-independent differentiation and apoptosis. Oncogene 15:1394–1406CrossRef Janson W, Brandner G, Siegel J (1997) Butyrate modulates DNA damage-induced p53 response by induction of p53-independent differentiation and apoptosis. Oncogene 15:1394–1406CrossRef
19.
Zurück zum Zitat Jolly AJ, Wild CP, Hardie LJ (2004) Acid and bile salts induce DNA damage in human oesophageal cell lines. Mutagenesis 19:319–324CrossRef Jolly AJ, Wild CP, Hardie LJ (2004) Acid and bile salts induce DNA damage in human oesophageal cell lines. Mutagenesis 19:319–324CrossRef
20.
Zurück zum Zitat Jurek D, Fleckl E, Marian B (2005) Bile acid induced gene expression in LT97 colonic adenoma cells. Food Chem Toxicol 43:87–93CrossRef Jurek D, Fleckl E, Marian B (2005) Bile acid induced gene expression in LT97 colonic adenoma cells. Food Chem Toxicol 43:87–93CrossRef
21.
Zurück zum Zitat de Kok TM, van Maanen JMS (2000) Evaluation of fecal mutagenicity and colorectal cancer risk. Mutat Res 463:53–101CrossRef de Kok TM, van Maanen JMS (2000) Evaluation of fecal mutagenicity and colorectal cancer risk. Mutat Res 463:53–101CrossRef
22.
Zurück zum Zitat Lowe GM, Booth LA, Young AJ, Bilton RF (1999) Lycopene and β-carotene protect against oxidative damage in HT29 cells at low concentrations but rapidly lose this capacity at higher doses. Free Rad Res 30:141–151CrossRef Lowe GM, Booth LA, Young AJ, Bilton RF (1999) Lycopene and β-carotene protect against oxidative damage in HT29 cells at low concentrations but rapidly lose this capacity at higher doses. Free Rad Res 30:141–151CrossRef
23.
Zurück zum Zitat Martinez JD, Stratagoules ED, La Rue JM, Powell AA, Gause PR, Craven MT, Payne CM, Powell MB, Gerner EW, Earnest DL (1998) Different bile acids exhibit distinct biological effects: the tumor promoter deoxycholic acid induces apoptosis and the chemopreventive agent ursodeoxycholic acid inhibits cell proliferation. Nutr Cancer 31:111–118CrossRef Martinez JD, Stratagoules ED, La Rue JM, Powell AA, Gause PR, Craven MT, Payne CM, Powell MB, Gerner EW, Earnest DL (1998) Different bile acids exhibit distinct biological effects: the tumor promoter deoxycholic acid induces apoptosis and the chemopreventive agent ursodeoxycholic acid inhibits cell proliferation. Nutr Cancer 31:111–118CrossRef
24.
Zurück zum Zitat McGarr SE, Ridlon JM, Hylemon PB (2005) Diet, anaerobic bacterial metabolism, and colon cancer: a review of the literature. J Clin Gastroenetrol 39:98–109 McGarr SE, Ridlon JM, Hylemon PB (2005) Diet, anaerobic bacterial metabolism, and colon cancer: a review of the literature. J Clin Gastroenetrol 39:98–109
25.
Zurück zum Zitat McMillan L, Butcher S, Wallis Y, Neoptolemos JP, Lord JM (2000) Bile acids reduce the apoptosis-inducing effects of sodium butyrate on human colon adenoma (AA/C1) cells: implications for colon carcinogenesis. Biochem Biophys Res Commun 273:45–49CrossRef McMillan L, Butcher S, Wallis Y, Neoptolemos JP, Lord JM (2000) Bile acids reduce the apoptosis-inducing effects of sodium butyrate on human colon adenoma (AA/C1) cells: implications for colon carcinogenesis. Biochem Biophys Res Commun 273:45–49CrossRef
26.
Zurück zum Zitat Narisawa T, Magadia NE, Weisburger JH, Wynder EL (1974) Promoting effects of bile acids on colon carcinogenesis after intrarectal instillation of N-methyl-N-nitroguanidine in rats. J Natl Cancer Inst 53:1093–1097 Narisawa T, Magadia NE, Weisburger JH, Wynder EL (1974) Promoting effects of bile acids on colon carcinogenesis after intrarectal instillation of N-methyl-N-nitroguanidine in rats. J Natl Cancer Inst 53:1093–1097
27.
Zurück zum Zitat Nordling MM, Glinghammar B, Karlsson PC (2003) Effect on cell proliferation, activator protein-1 and genotoxicity by fecal water from patients with colorectal adenomas. Scand J Gastroenterol 38:549–555CrossRef Nordling MM, Glinghammar B, Karlsson PC (2003) Effect on cell proliferation, activator protein-1 and genotoxicity by fecal water from patients with colorectal adenomas. Scand J Gastroenterol 38:549–555CrossRef
28.
Zurück zum Zitat Payne CM, Crowley C, Washostultz D, Briehl M, Bernstein H, Bernstein C, Beard S, Holubec H, Warneke J (1998) The stress-response proteins poly(ADP)ribose polymerase and NF-kB protect against bile salt-induced apoptosis. Cell Death Differ 5:623–636CrossRef Payne CM, Crowley C, Washostultz D, Briehl M, Bernstein H, Bernstein C, Beard S, Holubec H, Warneke J (1998) The stress-response proteins poly(ADP)ribose polymerase and NF-kB protect against bile salt-induced apoptosis. Cell Death Differ 5:623–636CrossRef
29.
Zurück zum Zitat Payne CM, Weber C, Crowley-Skillicorn C, Dvorak K, Bernstein H, Bernstein C, Holubec H, Dvorakova K, Garewal H, (2007) Deoxycholate induces mitochondrial oxidative stress and activates NF-(kappa)B through multiple mechanisms in HCT-116 colon epithelial cells. Carcinogenesis 28:215–222CrossRef Payne CM, Weber C, Crowley-Skillicorn C, Dvorak K, Bernstein H, Bernstein C, Holubec H, Dvorakova K, Garewal H, (2007) Deoxycholate induces mitochondrial oxidative stress and activates NF-(kappa)B through multiple mechanisms in HCT-116 colon epithelial cells. Carcinogenesis 28:215–222CrossRef
30.
Zurück zum Zitat Pongracz J, Clark P, Neoptolemos JP, Lord JM (1995) Expression of protein kinase C isoenzymes in colorectal cancer tissue and their differential activation by different bile acids. Int J Cancer 61:35–39CrossRef Pongracz J, Clark P, Neoptolemos JP, Lord JM (1995) Expression of protein kinase C isoenzymes in colorectal cancer tissue and their differential activation by different bile acids. Int J Cancer 61:35–39CrossRef
31.
Zurück zum Zitat Pool-Zobel BL, Abrahamse SL, Collins AR, Kark W, Gugler R, Oberreuther D, Siegel EG, Treptow-van Lishaut S, Rechkemmer G (2001) Analysis of DNA strand breaks, oxidised bases, and glutathione S-transferase P1 in human colon cells from biopsies. Cancer Epidemiol Biomarkers Prev 8:609–614 Pool-Zobel BL, Abrahamse SL, Collins AR, Kark W, Gugler R, Oberreuther D, Siegel EG, Treptow-van Lishaut S, Rechkemmer G (2001) Analysis of DNA strand breaks, oxidised bases, and glutathione S-transferase P1 in human colon cells from biopsies. Cancer Epidemiol Biomarkers Prev 8:609–614
32.
Zurück zum Zitat Pool-Zobel BL, Leucht U (1997) Induction of DNA damage by risk factors of colon cancer in human colon cells derived from biopsies. Mutat Res 375:105–115 Pool-Zobel BL, Leucht U (1997) Induction of DNA damage by risk factors of colon cancer in human colon cells derived from biopsies. Mutat Res 375:105–115
33.
Zurück zum Zitat Pool-Zobel BL, Selvaraju V, Sauer J, Kautenburger T, Kiefer J, Richter KK, Soom M, Wolfl S (2005) Butyrate may enhance toxicological defence in primary, adenoma and tumor human colon cells by favourably modulating expression of glutathione S-transferases genes, an approach in nutrigenomics. Carcinogenesis 26:1064–1076CrossRef Pool-Zobel BL, Selvaraju V, Sauer J, Kautenburger T, Kiefer J, Richter KK, Soom M, Wolfl S (2005) Butyrate may enhance toxicological defence in primary, adenoma and tumor human colon cells by favourably modulating expression of glutathione S-transferases genes, an approach in nutrigenomics. Carcinogenesis 26:1064–1076CrossRef
34.
Zurück zum Zitat Powolny A, Xu J, Loo G (2001) Deoxycholate induces DNA damage and apoptosis in human colon epithelial cells expressing either mutant or wild-type p53. Int J Biochem 33:193–203CrossRef Powolny A, Xu J, Loo G (2001) Deoxycholate induces DNA damage and apoptosis in human colon epithelial cells expressing either mutant or wild-type p53. Int J Biochem 33:193–203CrossRef
35.
Zurück zum Zitat Reddy BS (1995) Nutritional factors and colon cancer. Crit Rev Food Sci Nutr 35:175–190CrossRef Reddy BS (1995) Nutritional factors and colon cancer. Crit Rev Food Sci Nutr 35:175–190CrossRef
36.
Zurück zum Zitat Reddy BS, Narisawa T, Weisburger JH, Wynder EL (1976) Promoting effects of sodium deoxycholate on colon adeno-carcinomas in germfree rats. J Natl Cancer Inst 56:441–442 Reddy BS, Narisawa T, Weisburger JH, Wynder EL (1976) Promoting effects of sodium deoxycholate on colon adeno-carcinomas in germfree rats. J Natl Cancer Inst 56:441–442
37.
Zurück zum Zitat Rosignoli P, Fabiani R, De Bartolomeo A, Spinozzi F, Agea E, Pelli MA, Morozzi G (2001) Protective activity of butyrate on hydrogen peroxide-induced DNA damage in isolated human colonocytes and HT29 tumour cells. Carcinogenesis 22:1675–1680CrossRef Rosignoli P, Fabiani R, De Bartolomeo A, Spinozzi F, Agea E, Pelli MA, Morozzi G (2001) Protective activity of butyrate on hydrogen peroxide-induced DNA damage in isolated human colonocytes and HT29 tumour cells. Carcinogenesis 22:1675–1680CrossRef
38.
Zurück zum Zitat Ryu H, Lee J, Olofsson BA, Mwidau A, Dedeoglu A, Escudero M, Flemington E, Azizkhan-Clifford J, Ferrante RJ, Ratan RR (2003) Histone deacetylase inhibitors prevent oxidative neuronal death independent of expanded polyglutamine repeats via an Sp1-dependent pathway. Proc Natl Acad Sci USA 100:4281–4286CrossRef Ryu H, Lee J, Olofsson BA, Mwidau A, Dedeoglu A, Escudero M, Flemington E, Azizkhan-Clifford J, Ferrante RJ, Ratan RR (2003) Histone deacetylase inhibitors prevent oxidative neuronal death independent of expanded polyglutamine repeats via an Sp1-dependent pathway. Proc Natl Acad Sci USA 100:4281–4286CrossRef
39.
Zurück zum Zitat Scott DW, Mutamba S, Hopkins RG, Loo G (2005) Increased GADD gene expression in human colon epithelial cells exposed to deoxycholate. J Cell Physiol 202:295–303CrossRef Scott DW, Mutamba S, Hopkins RG, Loo G (2005) Increased GADD gene expression in human colon epithelial cells exposed to deoxycholate. J Cell Physiol 202:295–303CrossRef
40.
Zurück zum Zitat Sengupta S, Muir JG, Gibson BR (2006) Does butyrate protect from colorectal cancer? J Gastroenterol Hepathol 21: 209–219CrossRef Sengupta S, Muir JG, Gibson BR (2006) Does butyrate protect from colorectal cancer? J Gastroenterol Hepathol 21: 209–219CrossRef
41.
Zurück zum Zitat Singh NP, McCoy MT, Tice RR, Schneider EL (1988) A simple technique for quantitation of low levels of DNA damage in individual cells. Exp Cell Res 175:184–191CrossRef Singh NP, McCoy MT, Tice RR, Schneider EL (1988) A simple technique for quantitation of low levels of DNA damage in individual cells. Exp Cell Res 175:184–191CrossRef
42.
Zurück zum Zitat Trombetta A, Maggiora M, Martinasso G, Cotogni P, Canuto R, Muzio G (2007) Arachidonic and docosahexaenoic acids reduce the growth of A549 human lung-tumor cells increasing lipid peroxidation and PPARs. Chem Biol Interact 165:239–250CrossRef Trombetta A, Maggiora M, Martinasso G, Cotogni P, Canuto R, Muzio G (2007) Arachidonic and docosahexaenoic acids reduce the growth of A549 human lung-tumor cells increasing lipid peroxidation and PPARs. Chem Biol Interact 165:239–250CrossRef
43.
Zurück zum Zitat Velazquez OC, Seto RW, Choi J, Zhou D, Breen F, Fisher JD, Rombeau JL (1997) Butyrate inhibits deoxycholate-induced increase in colonic mucosal DNA and protein synthesis in vivo. Dis Colon Rectum 40:1368–1375CrossRef Velazquez OC, Seto RW, Choi J, Zhou D, Breen F, Fisher JD, Rombeau JL (1997) Butyrate inhibits deoxycholate-induced increase in colonic mucosal DNA and protein synthesis in vivo. Dis Colon Rectum 40:1368–1375CrossRef
44.
Zurück zum Zitat Velazquez OC, Zhou D, Seto RW, Jabbar A, Choi J, Ledere HM, Rombeau JL (1996) In vivo crypt surface hyperproliferation is decreased by butyrate and increased by deoxycholate in normal rat colon: associated in vivo effects on c-fos and c-jun expression. J Parenter Enteral Nutr 20:243–250CrossRef Velazquez OC, Zhou D, Seto RW, Jabbar A, Choi J, Ledere HM, Rombeau JL (1996) In vivo crypt surface hyperproliferation is decreased by butyrate and increased by deoxycholate in normal rat colon: associated in vivo effects on c-fos and c-jun expression. J Parenter Enteral Nutr 20:243–250CrossRef
45.
Zurück zum Zitat Venturi M, Hambly RJ, Glinghammar B, Rafter JJ, Rowland IR (1997) Genotoxic activity in human faecal water and the role of bile acids: a study using the alkaline comet assay. Carcinogenesis 18:2353–2359CrossRef Venturi M, Hambly RJ, Glinghammar B, Rafter JJ, Rowland IR (1997) Genotoxic activity in human faecal water and the role of bile acids: a study using the alkaline comet assay. Carcinogenesis 18:2353–2359CrossRef
46.
Zurück zum Zitat Weisburger JH, Reddy BS, Barnes WS, Wynder EL (1983) Bile acids, but not neutral sterols, are tumor promoters in the colon in man and in rodents. Environ Health Perspect 50: 101–107CrossRef Weisburger JH, Reddy BS, Barnes WS, Wynder EL (1983) Bile acids, but not neutral sterols, are tumor promoters in the colon in man and in rodents. Environ Health Perspect 50: 101–107CrossRef
47.
Zurück zum Zitat Wong JMW, de Souza R, Kendall CWC, Emam A, Jenkins DJA (2006) Colonic health: fermentation and short chain fatty acids. J Clin Gastroenterol 40:235–243CrossRef Wong JMW, de Souza R, Kendall CWC, Emam A, Jenkins DJA (2006) Colonic health: fermentation and short chain fatty acids. J Clin Gastroenterol 40:235–243CrossRef
48.
Zurück zum Zitat Zhang F, Subbaramaiah K, Altorki N, Dannenberg AJ (1998) Dihydroxy bile acids activate the transcription of cyclooxygenase-2. J Biol Chem 273:2424–2428CrossRef Zhang F, Subbaramaiah K, Altorki N, Dannenberg AJ (1998) Dihydroxy bile acids activate the transcription of cyclooxygenase-2. J Biol Chem 273:2424–2428CrossRef
Metadaten
Titel
Genotoxic effect of bile acids on human normal and tumour colon cells and protection by dietary antioxidants and butyrate
verfasst von
Patrizia Rosignoli
Roberto Fabiani
Angelo De Bartolomeo
Raffaela Fuccelli
Maria Antonietta Pelli
Guido Morozzi
Publikationsdatum
01.09.2008
Verlag
D. Steinkopff-Verlag
Erschienen in
European Journal of Nutrition / Ausgabe 6/2008
Print ISSN: 1436-6207
Elektronische ISSN: 1436-6215
DOI
https://doi.org/10.1007/s00394-008-0725-8

Weitere Artikel der Ausgabe 6/2008

European Journal of Nutrition 6/2008 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Notfall-TEP der Hüfte ist auch bei 90-Jährigen machbar

26.04.2024 Hüft-TEP Nachrichten

Ob bei einer Notfalloperation nach Schenkelhalsfraktur eine Hemiarthroplastik oder eine totale Endoprothese (TEP) eingebaut wird, sollte nicht allein vom Alter der Patientinnen und Patienten abhängen. Auch über 90-Jährige können von der TEP profitieren.

Niedriger diastolischer Blutdruck erhöht Risiko für schwere kardiovaskuläre Komplikationen

25.04.2024 Hypotonie Nachrichten

Wenn unter einer medikamentösen Hochdrucktherapie der diastolische Blutdruck in den Keller geht, steigt das Risiko für schwere kardiovaskuläre Ereignisse: Darauf deutet eine Sekundäranalyse der SPRINT-Studie hin.

Bei schweren Reaktionen auf Insektenstiche empfiehlt sich eine spezifische Immuntherapie

Insektenstiche sind bei Erwachsenen die häufigsten Auslöser einer Anaphylaxie. Einen wirksamen Schutz vor schweren anaphylaktischen Reaktionen bietet die allergenspezifische Immuntherapie. Jedoch kommt sie noch viel zu selten zum Einsatz.

Therapiestart mit Blutdrucksenkern erhöht Frakturrisiko

25.04.2024 Hypertonie Nachrichten

Beginnen ältere Männer im Pflegeheim eine Antihypertensiva-Therapie, dann ist die Frakturrate in den folgenden 30 Tagen mehr als verdoppelt. Besonders häufig stürzen Demenzkranke und Männer, die erstmals Blutdrucksenker nehmen. Dafür spricht eine Analyse unter US-Veteranen.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.