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上皮氧合增加将结肠炎与肿瘤发生细菌的扩张联系起来。

Increased Epithelial Oxygenation Links Colitis to an Expansion of Tumorigenic Bacteria.

机构信息

Department of Medical Microbiology and Immunology, School of Medicine, University of California at Davis, Davis, California, USA.

Department of Medical Microbiology and Immunology, School of Medicine, University of California at Davis, Davis, California, USA

出版信息

mBio. 2019 Oct 1;10(5):e02244-19. doi: 10.1128/mBio.02244-19.

Abstract

Intestinal inflammation is a risk factor for colorectal cancer formation, but the underlying mechanisms remain unknown. Here, we investigated whether colitis alters the colonic microbiota to enhance its cancer-inducing activity. Colitis increased epithelial oxygenation in the colon of mice and drove an expansion of within the gut-associated microbial community through aerobic respiration. An aerobic expansion of colibactin-producing was required for the cancer-inducing activity of this pathobiont in a mouse model of colitis-associated colorectal cancer formation. We conclude that increased epithelial oxygenation in the colon is associated with an expansion of a prooncogenic driver species, thereby increasing the cancer-inducing activity of the microbiota. One of the environmental factors important for colorectal cancer formation is the gut microbiota, but the habitat filters that control its cancer-inducing activity remain unknown. Here, we show that chemically induced colitis elevates epithelial oxygenation in the colon, thereby driving an expansion of colibactin-producing , a prooncogenic driver species. These data suggest that elevated epithelial oxygenation is a potential risk factor for colorectal cancer formation because the consequent changes in the gut habitat escalate the cancer-inducing activity of the microbiota.

摘要

肠道炎症是结直肠癌形成的一个风险因素,但其中的潜在机制尚不清楚。在这里,我们研究了结肠炎是否会改变结肠微生物群,从而增强其致癌活性。结肠炎增加了小鼠结肠上皮的氧合作用,并通过需氧呼吸驱动肠道相关微生物群落中 的扩张。在结肠炎相关结直肠癌形成的小鼠模型中,产 colibactin 的 的需氧扩张是该条件致病菌致癌活性所必需的。我们得出结论,结肠上皮氧合作用的增加与致癌驱动物种的扩张有关,从而增加了微生物群的致癌活性。影响结直肠癌形成的一个重要环境因素是肠道微生物群,但控制其致癌活性的栖息地滤器仍不清楚。在这里,我们表明,化学诱导的结肠炎会增加结肠上皮的氧合作用,从而驱动产 colibactin 的 的扩张,这是一种致癌驱动物种。这些数据表明,上皮氧合作用的升高可能是结直肠癌形成的一个潜在风险因素,因为肠道栖息地的相应变化会加剧微生物群的致癌活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2419/6775460/d27fd5f3a3c5/mBio.02244-19-f0001.jpg

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