Low colonic glutathione detoxification capacity in patients at risk for colon cancer

• Published in: European journal of clinical investigation 2006-03, Vol.36 (3), p.188-192
• Main Authors: Grubben, M. J. A. L., van Den Braak, C. C. M., Nagengast, F. M., Peters, W. H. M.
• Format: Article
• Language: English
• Subjects: Adenoma; Adenoma - chemistry; Adenoma - enzymology; Adenomatous Polyposis Coli - chemistry; Adenomatous Polyposis Coli - enzymology; Adult; Biological and medical sciences; Colon - chemistry; Colon - enzymology; colon cancer; Colonic Neoplasms - chemistry; Colonic Neoplasms - enzymology; Colorectal Neoplasms - chemistry; Colorectal Neoplasms - enzymology; Colorectal Neoplasms, Hereditary Nonpolyposis - chemistry; Colorectal Neoplasms, Hereditary Nonpolyposis - enzymology; FAP; Female; Gastroenterology. Liver. Pancreas. Abdomen; General aspects; glutathione; Glutathione - analysis; glutathione S-transferase; Glutathione Transferase - metabolism; HNPCC; Humans; Intestinal Mucosa - chemistry; Intestinal Mucosa - enzymology; Male; Medical sciences; Middle Aged; Risk Factors; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Tumors
• ISSN: 0014-2972; 1365-2362
• DOI: 10.1111/j.1365-2362.2006.01618.x

Background  Colon carcinogenesis is a multifactorial process influenced by hereditary as well as environmental factors. The glutathione/glutathione S‐transferase detoxification system in the colon is important for protection against carcinogens. We investigated the levels of glutathione/glutathione S‐transferase in normal colon mucosa of patients with colorectal cancer and in patients at high risk for colorectal cancer compared with those in healthy controls. Materials and methods  Glutathione content was analyzed by high‐performance liquid chromatography, and glutathione S‐transferase enzyme activity by spectrophotometric determination with 1‐chloro 2,4‐dinitrobenzene. Normal colon tissue of patients with colon adenoma (n = 64), colorectal cancer (n = 37), familial adenomatous polyposis (FAP; n = 19), hereditary non‐polyposis colorectal cancer families with (HNPCC+Ad; n = 34) or without (HNPCC‐Ad; n = 33) adenoma was investigated. Results  Glutathione levels were significantly lower in the normal colon mucosa of patients with cancer, FAP, HNPCC‐Ad or HNPCC+Ad compared with adenoma patients or healthy controls. Glutathione S‐transferase enzyme activity in the distal colon was significantly lower in patients with cancer or FAP compared with the adenoma patients or healthy controls, whereas values in carcinoma patients were significantly lower compared with both the HNPCC‐Ad and HNPCC+Ad groups. Conclusions  An association of low colonic glutathione/glutathione S‐transferase activity levels and high clinical risk for the development of colorectal cancer was observed. This low glutathione detoxification capacity might contribute to the colon cancer risk.