Department of Toxicogenomics, Maastricht University, P.O. Box 616, 6200 MD Maastricht, The Netherlands.
Food Chem Toxicol. 2012 Feb;50(2):95-103. doi: 10.1016/j.fct.2011.10.038. Epub 2011 Oct 14.
Red meat consumption is associated with an increased colorectal cancer (CRC) risk, which may be due to an increased endogenous formation of genotoxic N-nitroso compounds (NOCs). To assess the impact of red meat consumption on potential risk factors of CRC, we investigated the effect of a 7-day dietary red meat intervention in human subjects on endogenous NOC formation and fecal water genotoxicity in relation to genome-wide transcriptomic changes induced in colonic tissue. The intervention showed no effect on fecal NOC excretion but fecal water genotoxicity significantly increased in response to red meat intake. Colonic inflammation caused by inflammatory bowel disease, which has been suggested to stimulate endogenous nitrosation, did not influence fecal NOC excretion or fecal water genotoxicity. Transcriptomic analyses revealed that genes significantly correlating with the increase in fecal water genotoxicity were involved in biological pathways indicative of genotoxic effects, including modifications in DNA damage repair, cell cycle, and apoptosis pathways. Moreover, WNT signaling and nucleosome remodeling pathways were modulated which are implicated in human CRC development. We conclude that the gene expression changes identified in this study corroborate the genotoxic potential of diets high in red meat and point towards a potentially increased CRC risk in humans.
红肉消费与结直肠癌(CRC)风险增加有关,这可能是由于内源性遗传毒性 N-亚硝基化合物(NOC)的形成增加。为了评估红肉消费对 CRC 潜在风险因素的影响,我们研究了 7 天的饮食红肉干预对人类受试者内源性 NOC 形成和粪便水遗传毒性的影响,以及对结肠组织中诱导的全基因组转录组变化的影响。该干预措施对粪便 NOC 排泄没有影响,但红肉摄入后粪便水遗传毒性显著增加。炎症性肠病引起的结肠炎症曾被认为会刺激内源性亚硝化作用,但它不会影响粪便 NOC 排泄或粪便水遗传毒性。转录组分析显示,与粪便水遗传毒性增加显著相关的基因参与了与遗传毒性作用相关的生物途径,包括 DNA 损伤修复、细胞周期和细胞凋亡途径的改变。此外,还调节了 WNT 信号转导和核小体重塑途径,这些途径与人类 CRC 的发展有关。我们得出结论,本研究中鉴定的基因表达变化证实了富含红肉的饮食具有遗传毒性潜力,并指出人类 CRC 风险可能增加。