4.7 Article

Gamma-tocopherol attenuates moderate but not severe colitis and suppresses moderate colitis-promoted colon tumorigenesis in mice

Journal

FREE RADICAL BIOLOGY AND MEDICINE
Volume 65, Issue -, Pages 1069-1077

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2013.08.187

Keywords

Vitamin E; Tocopherol; Carboxychromanol; Inflammation; Colon cancer; Colitis

Funding

  1. NCI [R21CA152588, R21CA133651, R01AT006882]
  2. NCCAM of National Institutes of Health

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Inflammation can promote colon cancer. Mechanistic studies indicate that gamma-tocopherol (gamma T), a major form of vitamin E in diets, has anti-inflammatory and anticancer properties. Here we investigated the effectiveness of gamma T and a mixture of tocopherols against colitis and colitis-promoted colon tumorigenesis in male BALB/c mice. gamma T or mixed tocopherols (at 0.1% diet) did not show any effect on colon tumorigenesis induced by azoxymethane (AOM, 10 mg/kg) with three cycles of dextran sodium sulfate (DSS at 1.5-2.5%). gamma T failed to exhibit protection of severe colitis caused by three cycles of DSS at 2.5%. In contrast, when AOM-initiated carcinogenesis was promoted by relatively mild colitis induced by one-cycle DSS (1.5%), gamma T, but not mixed tocopherols, suppressed total multiplicity of macroscopic adenomas (P=0.06) and large adenomatous polyps (> 2 mm(2), P < 0.05) by 60 and 85%, respectively. gamma T also significantly decreased tumor multiplicity (>2 mm(2)) induced by AOM with two cycles of 1.5% DSS even when dietary supplementation was started after AOM injection. Consistently, gamma T but not mixed tocopherols attenuated DSS (1.5%)-induced colon inflammation and damage as well as formation of atypical glandular byperplasia. Mice supplemented with tocopherols had high fecal excretion of 13'-carboxychromanol, a long-chain vitamin E metabolite shown to have potent anti-inflammatory activities. Our study demonstrates that gamma T is able to alleviate moderate but not severe colitis and its promoted tumorigenesis, and indicates that inflammation severity should be considered in evaluating anticancer effectiveness of chemoprevention agents. (C) 2013 Elsevier Inc. All rights reserved.

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