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Intestinal Inflammation Targets Cancer-Inducing Activity of the Microbiota

机译:肠道炎症针对微生物群的癌症诱导活性。

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摘要

Inflammation alters host physiology to promote cancer, as seen in colitis-associated colorectal cancer (CRC). Here, we identify the intestinal microbiota as a target of inflammation that affects the progression of CRC. High-throughput sequencing revealed that inflammation modifies gut microbial composition in colitis-susceptible interleukin-10-deficient (Il 10~(-/-)) mice. Monocolonization with the commensal Escherichia coli NC101 promoted invasive carcinoma in azoxymethane (AOM)-treated Il10~(-/-) mice. Deletion of the polyketide synthase (pks) genotoxic island from E. coli NC101 decreased tumor multiplicity and invasion in AOM/Il10~(-/-) mice, without altering intestinal inflammation. Mucosa-associated pks~+ E. coli were found in a significantly high percentage of inflammatory bowel disease and CRC patients. This suggests that in mice, colitis can promote tumorigenesis by altering microbial composition and inducing the expansion of microorganisms with genotoxic capabilities.
机译:如结肠炎相关的大肠癌(CRC)所示,炎症会改变宿主的生理状况,从而促进癌症的发展。在这里,我们确定肠道菌群是影响CRC进展的炎症目标。高通量测序表明,炎症改变了易患结肠炎的白细胞介素10缺乏症(Il 10〜(-/-))小鼠的肠道微生物组成。共生大肠埃希氏菌NC101的单结肠化促进了乙氧甲烷(AOM)处理的Il10〜(-/-)小鼠的浸润性癌。从大肠杆菌NC101中删除聚酮化合物合酶(pks)基因毒性岛可降低AOM / Il10〜(-/-)小鼠的肿瘤多样性和侵袭能力,而不会改变肠道炎症。在炎症性肠病和CRC患者中发现了与粘膜相关的pks〜+大肠杆菌。这表明在小鼠中,结肠炎可通过改变微生物组成并诱导具有遗传毒性能力的微生物的扩增来促进肿瘤发生。

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  • 来源
    《Science》 |2012年第6103期|p.120-123|共4页
  • 作者单位

    Department of Medicine, Pharmacology and Immunology-Microbiology, University of North Carolina at Chapel Hill,Chapel Hill, NC 27599, USA.;

    Department of Medicine, Pharmacology and Immunology-Microbiology, University of North Carolina at Chapel Hill,Chapel Hill, NC 27599, USA.;

    Department of Medicine, Pharmacology and Immunology-Microbiology, University of North Carolina at Chapel Hill,Chapel Hill, NC 27599, USA.;

    Department of Medicine, Pharmacology and Immunology-Microbiology, University of North Carolina at Chapel Hill,Chapel Hill, NC 27599, USA.;

    Department of Medicine, Pharmacology and Immunology-Microbiology, University of North Carolina at Chapel Hill,Chapel Hill, NC 27599, USA.;

    Department of Medicine, Pharmacology and Immunology-Microbiology, University of North Carolina at Chapel Hill,Chapel Hill, NC 27599, USA.;

    Department of Gastroenterology,University of Liverpool, Liverpool L69 3BX, UK.;

    Ottawa Institute of Systems Biology, Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ontario K1H 8M5, Canada,Department of Medical Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah 21589, Saudi Arabia;

    Department of Clinical Sciences, Cornell University, Ithaca, NY 14853, USA.;

    Lineberger Comprehensive Cancer Center, Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.;

    Department of Gastroenterology,University of Liverpool, Liverpool L69 3BX, UK.;

    Ottawa Institute of Systems Biology, Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ontario K1H 8M5, Canada;

    Department of Clinical Sciences, Cornell University, Ithaca, NY 14853, USA.;

    Department of Medicine, Pharmacology and Immunology-Microbiology, University of North Carolina at Chapel Hill,Chapel Hill, NC 27599, USA.;

    Department of Medicine, Pharmacology and Immunology-Microbiology, University of North Carolina at Chapel Hill,Chapel Hill, NC 27599, USA.;

    Department of Bioinformatics and Genomics, University of North Carolina at Charlotte, Charlotte, NC 28223, USA.;

    Department of Medicine, Pharmacology and Immunology-Microbiology, University of North Carolina at Chapel Hill,Chapel Hill, NC 27599, USA.;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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