Silibinin modulates biotransforming microbial enzymes and prevents 1,2-dimethylhydrazine-induced preneoplastic changes in experimental colon cancer

Chemoprevention directed towards the control of colon carcinogenesis in its early stages should ultimately provide a higher quality of life for people than waiting to treat end-stage disease. Silibinin is a major bioactive compound that is present in the widely consumed dietary supplement Silymarin. The current investigation aimed to explore the effect of the phytochemical silibinin on the suppression of 1,2-dimethylhydrazine-induced colonic preneoplastic changes in a long-term preclinical model. Wistar male rats were divided into six groups: group 1 were control rats, group 2 were control rats that received silibinin alone (50 mg/kg body weight orally everyday), rats in group 3 were injected once weekly with 1,2-dimethylhydrazine (20 mg/kg body weight, subcutaneously 15 times), in addition, group 4 (initiation), group 5 (post initiation) and group 6 (entire period) received silibinin as in group 2. At the end of 32 weeks, the activities of the colonic and faecal biotransforming microbial enzymes were analysed. Modulatory effects were also evaluated using aberrant crypt foci (ACF), dysplastic ACF and tumour incidence as endpoint markers. Silibinin markedly reduced tumour incidence, as compared with the rats treated with unsupplemented 1,2-dimethylhydrazine. The most pronounced inhibition of ACF and dysplastic ACF development was observed in the rats fed with silibinin for the entire period and also during the post initiation period. Silibinin administration also significantly (P<0.05) modulated the biotransforming activity of microbial enzymes. The results of our study suggest that silibinin suppresses 1,2-dimethylhydrazine-induced colon carcinogenesis at various stages and exerts a potential chemopreventive action against colon cancer.

[1]  Sei-Jung Lee,et al.  A 116-kDa phytoglycoprotein inhibits aberrant crypt foci formation through modulation of manganese superoxide dismutase, inducible nitric oxide synthase, cyclooxygenase-2, nuclear factor-kappa B, activator protein-1, and proliferating cell nuclear antigen in 1,2-dimethylhydrazine/dextran sodium sulf , 2008, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

[2]  N. Nalini,et al.  Aberrant crypt foci and AgNORs as putative biomarkers to evaluate the chemopreventive efficacy of pronyl-lysine in rat colon carcinogenesis , 2008, Investigational New Drugs.

[3]  R. Agarwal,et al.  Inhibition of Azoxymethane-Induced Colonic Aberrant Crypt Foci Formation by Silibinin in Male Fisher 344 Rats , 2007, Cancer Prevention Research.

[4]  Yuan-Kun Lee,et al.  Effect of tea phenolics and their aromatic fecal bacterial metabolites on intestinal microbiota. , 2006, Research in microbiology.

[5]  S. Bhattacharya,et al.  Chemopreventive potential of diallylsulfide, lycopene and theaflavin during chemically induced colon carcinogenesis in rat colon through modulation of cyclooxygenase-2 and inducible nitric oxide synthase pathways , 2006, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

[6]  N. Nalini,et al.  Dietary supplementation of resveratrol suppresses colonic tumour incidence in 1,2-dimethylhydrazine-treated rats by modulating biotransforming enzymes and aberrant crypt foci development , 2006, British Journal of Nutrition.

[7]  K. Quek,et al.  Colorectal cancer in Asians: a demographic and anatomic survey in Malaysian patients undergoing colonoscopy , 2005, Alimentary pharmacology & therapeutics.

[8]  H. Nakagama,et al.  Modeling human colon cancer in rodents using a food‐borne carcinogen, PhIP , 2005, Cancer science.

[9]  A. Hara,et al.  Significance and role of early-lesions in experimental colorectal carcinogenesis. , 2005, Chemico-biological interactions.

[10]  T. Sugimura,et al.  Differential staining of dysplastic aberrant crypt foci in the colon facilitates prediction of carcinogenic potentials of chemicals in rats. , 2005, Cancer letters.

[11]  A. Wolk,et al.  Fruits, vegetables and risk of renal cell carcinoma: A prospective study of Swedish women , 2005, International journal of cancer.

[12]  M. Suzui,et al.  Histological and immunohistochemical observations of mucin‐depleted foci (MDF) stained with Alcian blue, in rat colon carcinogenesis induced with 1,2‐dimethylhydrazine dihydrochloride , 2004, Cancer science.

[13]  N. Nalini,et al.  Effect of coconut cake on the bacterial enzyme activity in 1,2-dimethyl hydrazine induced colon cancer. , 2004, Clinica chimica acta; international journal of clinical chemistry.

[14]  I. Rowland,et al.  Microbial-gut interactions in health and disease. Gastrointestinal cancer. , 2004, Best practice & research. Clinical gastroenterology.

[15]  V. Menon,et al.  Fenugreek affects the activity of β‐glucuronidase and mucinase in the colon , 2003 .

[16]  A. Scalbert,et al.  Absorption and metabolism of polyphenols in the gut and impact on health. , 2002, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

[17]  S. Salminen,et al.  Effect of Probiotics on Constipation, Fecal Azoreductase Activity and Fecal Mucin Content in the Elderly , 2002, Annals of Nutrition and Metabolism.

[18]  W. Walker,et al.  Nutritional impact of pre- and probiotics as protective gastrointestinal organisms. , 2002, Annual review of nutrition.

[19]  Dong-Hyun Kim,et al.  Intestinal bacterial β-glucuronidase activity of patients with colon cancer , 2001 .

[20]  J. Féher,et al.  Effect of silibinin and vitamin E on restoration of cellular immune response after partial hepatectomy. , 2001, Journal of ethnopharmacology.

[21]  Sang-Myeong Lee,et al.  Effects of Lactic Acid Bacteria on Intestinal Microbial Enzyme Activity and Composition in Rats Treated with Azoxymethane , 2001 .

[22]  B. Deplancke,et al.  Microbial modulation of innate defense: goblet cells and the intestinal mucus layer. , 2001, The American journal of clinical nutrition.

[23]  A. Medline,et al.  Possible mechanisms relating diet and risk of colon cancer. , 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[24]  R. Agarwal,et al.  Anti-angiogenic potential of a cancer chemopreventive flavonoid antioxidant, silymarin: inhibition of key attributes of vascular endothelial cells and angiogenic cytokine secretion by cancer epithelial cells. , 2000, Biochemical and biophysical research communications.

[25]  B. Halliwell,et al.  The gastrointestinal tract: A major site of antioxidant action? , 2000, Free radical research.

[26]  R. Rowland,et al.  Metabolic Activities of the Gut Microflora in Relation to Cancer , 2000 .

[27]  R. Agarwal,et al.  Significant inhibition by the flavonoid antioxidant silymarin against 12‐O‐tetradecanoylphorbol 13‐acetate–caused modulation of antioxidant and inflammatory enzymes, and cyclooxygenase 2 and interleukin‐1α expression in SENCAR mouse epidermis: Implications in the prevention of stage I tumor promotio , 1999, Molecular carcinogenesis.

[28]  G. Macfarlane,et al.  Ecological and physiological studies on large intestinal bacteria in relation to production of hydrolytic and reductive enzymes involved in formation of genotoxic metabolites. , 1998, Journal of medical microbiology.

[29]  P. Suter,et al.  Inhibitory action of silibinin on low density lipoprotein oxidation. , 1998, Arzneimittel-Forschung.

[30]  I. Rowland,et al.  Effect of Bifidobacterium longum and inulin on gut bacterial metabolism and carcinogen-induced aberrant crypt foci in rats. , 1998, Carcinogenesis.

[31]  I R Rowland,et al.  Genotoxic activity in human faecal water and the role of bile acids: a study using the alkaline comet assay. , 1997, Carcinogenesis.

[32]  I. Rowland,et al.  Influence of diets containing high and low risk factors for colon cancer on early stages of carcinogenesis in human flora-associated (HFA) rats. , 1997, Carcinogenesis.

[33]  M. Onoue,et al.  Specific species of intestinal bacteria influence the induction of aberrant crypt foci by 1,2-dimethylhydrazine in rats. , 1997, Cancer letters.

[34]  K. Kinzler,et al.  Lessons from Hereditary Colorectal Cancer , 1996, Cell.

[35]  H. Esumi,et al.  Emergence of adenomatous aberrant crypt foci (ACF) from hyperplastic ACF with concomitant increase in cell proliferation. , 1995, Cancer research.

[36]  R P Bird,et al.  Role of aberrant crypt foci in understanding the pathogenesis of colon cancer. , 1995, Cancer letters.

[37]  W. Ling Diet and colonic microflora interaction in colorectal cancer , 1995 .

[38]  T. P. Pretlow,et al.  Carcinoembryonic antigen in human colonic aberrant crypt foci. , 1994, Gastroenterology.

[39]  S. Gallinger,et al.  Somatic APC and K-ras codon 12 mutations in aberrant crypt foci from human colons. , 1994, Cancer research.

[40]  A. Manning,et al.  Sodium butyrate induces apoptosis in human colonic tumour cell lines in a p53‐independent pathway: Implications for the possible role of dietary fibre in the prevention of large‐bowel cancer , 1993, International journal of cancer.

[41]  C. Asselin,et al.  Regulation of C-fos expression by sodium butyrate in the human colon carcinoma cell line Caco-2. , 1993, Biochemical and biophysical research communications.

[42]  L. Thompson,et al.  Flaxseed supplementation and early markers of colon carcinogenesis. , 1992, Cancer letters.

[43]  H. Freeman Effects of differing purified cellulose, pectin, and hemicellulose fiber diets on fecal enzymes in 1,2-dimethylhydrazine-induced rat colon carcinogenesis. , 1986, Cancer research.

[44]  I. Rowland,et al.  The influence of the host on expression of intestinal microbial enzyme activities involved in metabolism of foreign compounds. , 1985, The Journal of applied bacteriology.

[45]  R. Nelson,et al.  Protective Role of Faecal pH in Experimental Colon Carcinogenesis , 1985, Journal of the Royal Society of Medicine.

[46]  I. Rowland,et al.  A comparison of the activity of five microbial enzymes in cecal content from rats, mice, and hamsters, and response to dietary pectin. , 1983, Toxicology and applied pharmacology.

[47]  B. Goldin,et al.  Alterations in fecal microflora enzymes related to diet, age, lactobacillus supplements, and dimethylhydrazine , 1977, Cancer.

[48]  E. Fiala Investigations into the metabolism and mode of action of the colon carcinogens 1,2‐dimethylhydrazine and azoxymethane , 1977, Cancer.

[49]  B. Goldin,et al.  The relationship between diet and rat fecal bacterial enzymes implicated in colon cancer. , 1976, Journal of the National Cancer Institute.

[50]  E. Wynder,et al.  Animal models for the study of dietary factors and cancer of the large bowel. , 1975, Cancer research.

[51]  R. Kato,et al.  Studies on the mechanism of nitro reduction by rat liver. , 1969, Molecular pharmacology.

[52]  J. Gillette,et al.  Mechanism of p-nitrobenzoate reduction in liver: the possible role oc cytochrome P-450 in liver microsomes. , 1968, Molecular pharmacology.

[53]  Oliver H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.

[54]  Norton Nelson,et al.  A PHOTOMETRIC ADAPTATION OF THE SOMOGYI METHOD FOR THE DETERMINATION OF GLUCOSE , 1944 .

[55]  V. Balasubramaniyan,et al.  Rat colonic lipid peroxidation and antioxidant status: the effects of dietary luteolin on 1,2-dimethylhydrazine challenge. , 2005, Cellular & molecular biology letters.

[56]  Philippe Sansonetti,et al.  Microbial-gut interactions in health and disease. Epithelial cell responses. , 2004, Best practice & research. Clinical gastroenterology.

[57]  V. Menon,et al.  Fenugreek affects the activity of beta-glucuronidase and mucinase in the colon. , 2003, Phytotherapy research : PTR.

[58]  D. Kim,et al.  Intestinal bacterial beta-glucuronidase activity of patients with colon cancer. , 2001, Archives of pharmacal research.

[59]  J. Rafter,et al.  Cellular toxicity of human faecal water--possible role in aetiology of colon cancer. , 1987, Scandinavian journal of gastroenterology. Supplement.

[60]  B. Goldin In situ bacterial metabolism and colon mutagens. , 1986, Annual review of microbiology.

[61]  S. Shiau,et al.  Effects of Dietary Fiber on Fecal Mucinase and β-Glucuronidase Activity in Rats , 1983 .

[62]  Evans El Acute Striae Atrophicae. , 1915 .