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Patients with familial adenomatous polyposis harbor colonic biofilms containing tumorigenic bacteria

机译:家族性腺瘤性息肉病患者的结肠生物膜中含有致癌细菌

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摘要

Individuals with sporadic colorectal cancer (CRC) frequently harbor abnormalities in the composition of the gut microbiome; however, the microbiota associated with precancerous lesions in hereditary CRC remains largely unknown. We studied colonic mucosa of patients with familial adenomatous polyposis (FAP), who develop benign precursor lesions (polyps) early in life. We identified patchy bacterial biofilms composed predominately of Escherichia coli and Bacteroides fragilis. Genes for colibactin (clbB) and Bacteroides fragilis toxin (bft), encoding secreted oncotoxins, were highly enriched in FAP patients' colonic mucosa compared to healthy individuals. Tumor-prone mice cocolonized with E. coli (expressing colibactin), and enterotoxigenic B. fragilis showed increased interleukin-17 in the colon and DNA damage in colonic epithelium with faster tumor onset and greater mortality, compared to mice with either bacterial strain alone. These data suggest an unexpected link between early neoplasia of the colon and tumorigenic bacteria.
机译:散发性结直肠癌(CRC)患者的肠道微生物组组成经常出现异常。然而,与遗传性CRC癌前病变相关的微生物群在很大程度上仍然未知。我们研究了家族性腺瘤性息肉病(FAP)患者的结肠黏膜,他们在生命的早期发展为良性前体病变(息肉)。我们确定了斑驳的细菌生物膜,主要由大肠杆菌和脆弱的拟杆菌组成。与健康人相比,FAP患者的结肠粘膜中富含大肠杆菌杆菌素(clbB)和脆弱拟杆菌杆菌(bft)的基因,它们编码分泌的真菌毒素。与单独使用任何一种细菌菌株的小鼠相比,用大肠杆菌(表达大肠杆菌杆菌)和脆弱的肠毒素的结肠炎结肠炎易肿瘤小鼠显示结肠中的白介素17升高,结肠上皮中的DNA损伤增加,肿瘤发作更快,死亡率更高。这些数据表明结肠的早期肿瘤形成与致瘤细菌之间存在出乎意料的联系。

著录项

  • 来源
    《Science》 |2018年第6375期|592-597|共6页
  • 作者单位

    Johns Hopkins Univ, Bloomberg Kimmel Inst Canc Immunotherapy, Baltimore, MD 21218 USA;

    Johns Hopkins Univ, Bloomberg Kimmel Inst Canc Immunotherapy, Baltimore, MD 21218 USA;

    Johns Hopkins Univ, Dept Environm Hlth Sci, Bloomberg Sch Publ Hlth, Baltimore, MD 21205 USA;

    Johns Hopkins Univ, Bloomberg Kimmel Inst Canc Immunotherapy, Baltimore, MD 21218 USA;

    Radboud Univ Nijmegen, Dept Pathol, Med Ctr, Postbus 9101, NL-6500 HB Nijmegen, Netherlands;

    Johns Hopkins Univ, Bloomberg Kimmel Inst Canc Immunotherapy, Baltimore, MD 21218 USA;

    Johns Hopkins Univ, Bloomberg Kimmel Inst Canc Immunotherapy, Baltimore, MD 21218 USA;

    Johns Hopkins Univ, Bloomberg Kimmel Inst Canc Immunotherapy, Baltimore, MD 21218 USA;

    Johns Hopkins Univ, Dept Surg, Baltimore, MD USA;

    Johns Hopkins Univ, Dept Mol & Comparat Pathobiol, Baltimore, MD USA;

    Johns Hopkins Univ, Dept Pathol, Baltimore, MD USA;

    Johns Hopkins Univ, Dept Oncol, Baltimore, MD 21218 USA;

    Johns Hopkins Univ, Dept Surg, Baltimore, MD USA;

    Johns Hopkins Univ, Bloomberg Kimmel Inst Canc Immunotherapy, Baltimore, MD 21218 USA;

    Johns Hopkins Univ, Bloomberg Kimmel Inst Canc Immunotherapy, Baltimore, MD 21218 USA;

    Johns Hopkins Univ, Bloomberg Kimmel Inst Canc Immunotherapy, Baltimore, MD 21218 USA;

    Johns Hopkins Univ, Bloomberg Kimmel Inst Canc Immunotherapy, Baltimore, MD 21218 USA;

    Johns Hopkins Univ, Bloomberg Kimmel Inst Canc Immunotherapy, Baltimore, MD 21218 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);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 02:51:01

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