Carcinogenesis Advance Access originally published online on March 3, 2005
Carcinogenesis 2005 26(6):1064-1076; doi:10.1093/carcin/bgi059
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Carcinogenesis vol.26 no.6 © Oxford University Press 2005; all rights reserved.
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
Department of Nutritional Toxicology, Institute for Nutrition, Friedrich-Schiller-University, Dornburger Strasse 25, D-07743 Jena, Germany, 1 Department of General and Visceral Surgery, Clinic for Surgery and 2 Department of Molecular Medicine, Clinic for Internal Medicine II, Friedrich-Schiller-University, Erlanger Allee 101, D-07743 Jena, Germany
* To whom correspondence should be addressed. Tel: + 49 3641 949670; Fax: + 49 3641 949672; Email: b8pobe{at}uni-jena.de
Butyrate, formed by bacterial fermentation of plant foods, has been suggested to reduce colon cancer risks by suppressing the proliferation of tumor cells. In addition, butyrate has been shown to induce glutathione S-transferases (GSTs) in tumor cell lines, which may contribute to the detoxification of dietary carcinogens. We hypothesize that butyrate also affects biotransformation in non-transformed colon cells. Thus, we have investigated the gene expression of drug metabolism genes in primary human colon tissue, premalignant LT97 adenoma and HT29 tumor cells cultured in an appropriate medium±butyrate. A total of 96 drug metabolism genes (including 12 GSTs) spotted on cDNA macroarrays (Superarray®; n = 3) were hybridized with biotin-labeled cDNA probes. To validate the expression detected with Superarray®, samples of LT97 cells were also analyzed with high density microarrays (Affymetrix® U133A), which include biotransformation genes that overlap with the set of genes represented on the Superarray®. Relative expression levels were compared across colon samples and for each colon sample±butyrate. Compared with fresh tissue, 13 genes were downregulated in primary cells cultivated ex vivo, whereas 8 genes were upregulated. Several genes were less expressed in LT97 (40 genes) or in HT29 (41 and 17 genes, grown for 72 and 48 h, respectively) compared with primary colon tissue. Butyrate induced GSTP1, GSTM2, and GSTA4 in HT29 as previously confirmed by other methods (northern blot/qPCR). We detected an upregulation of GSTs (GSTA2, GSTT2) that are known to be involved in the defence against oxidative stress in primary cells upon incubation with butyrate. The changes in expression detected in LT97 by Superarray® and Affymetrix® were similar, confirming the validity of the results. We conclude that low GST expression levels were favourably altered by butyrate. An induction of the toxicological defence system possibly contributes to reported chemopreventive properties of butyrate, a product of dietary fibre fermentation in the gut.
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