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结直肠癌中的宿主-微生物群失调。

Host-microbiota maladaptation in colorectal cancer.

机构信息

Kennedy Institute of Rheumatology, University of Oxford, Oxford, UK.

出版信息

Nature. 2020 Sep;585(7826):509-517. doi: 10.1038/s41586-020-2729-3. Epub 2020 Sep 23.


DOI:10.1038/s41586-020-2729-3
PMID:32968260
Abstract

Colorectal cancer (CRC) is a heterogeneous disease of the intestinal epithelium that is characterized by the accumulation of mutations and a dysregulated immune response. Up to 90% of disease risk is thought to be due to environmental factors such as diet, which is consistent with a growing body of literature that describes an 'oncogenic' CRC-associated microbiota. Whether this dysbiosis contributes to disease or merely represents a bystander effect remains unclear. To prove causation, it will be necessary to decipher which specific taxa or metabolites drive CRC biology and to fully characterize the underlying mechanisms. Here we discuss the host-microbiota interactions in CRC that have been reported so far, with particular focus on mechanisms that are linked to intestinal barrier disruption, genotoxicity and deleterious inflammation. We further comment on unknowns and on the outstanding challenges in the field, and how cutting-edge technological advances might help to overcome these. More detailed mechanistic insights into the complex CRC-associated microbiota would potentially reveal avenues that can be exploited for clinical benefit.

摘要

结直肠癌(CRC)是一种异质性的肠道上皮疾病,其特征是突变的积累和免疫反应失调。高达 90%的疾病风险被认为是由于环境因素,如饮食,这与越来越多的文献描述了一个“致癌”CRC 相关的微生物群。这种生态失调是否有助于疾病,还是仅仅代表一种旁观者效应,目前尚不清楚。要证明因果关系,就有必要破译哪些特定的分类群或代谢物驱动 CRC 生物学,并充分描述潜在的机制。在这里,我们讨论了迄今为止报道的 CRC 中的宿主-微生物群相互作用,特别关注与肠道屏障破坏、遗传毒性和有害炎症相关的机制。我们进一步评论了该领域的未知和悬而未决的挑战,以及尖端技术进步如何帮助克服这些挑战。对复杂的 CRC 相关微生物群的更详细的机制见解可能会揭示可以用于临床获益的途径。

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[2]
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[3]
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[4]
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[5]
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[8]
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[10]
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本文引用的文献

[1]
Gut microbiota modulation: a novel strategy for prevention and treatment of colorectal cancer.

Oncogene. 2020-6-8

[2]
Multi-omic profiling reveals associations between the gut mucosal microbiome, the metabolome, and host DNA methylation associated gene expression in patients with colorectal cancer.

BMC Microbiol. 2020-4-23

[3]
Full-repertoire comparison of the microscopic objects composing the human gut microbiome with sequenced and cultured communities.

J Microbiol. 2020-5

[4]
Colorectal cancer-associated anaerobic bacteria proliferate in tumor spheroids and alter the microenvironment.

Sci Rep. 2020-3-24

[5]
Metaproteomics characterizes human gut microbiome function in colorectal cancer.

NPJ Biofilms Microbiomes. 2020-3-24

[6]
Host responses to mucosal biofilms in the lung and gut.

Mucosal Immunol. 2020-5

[7]
Colorectal cancer diagnostic model utilizing metagenomic and metabolomic data of stool microbial extracellular vesicles.

Sci Rep. 2020-2-18

[8]
Cell-type-specific signaling networks in heterocellular organoids.

Nat Methods. 2020-2-17

[9]
Distinct microbial and immune niches of the human colon.

Nat Immunol. 2020-2-17

[10]
Endogenous murine microbiota member Faecalibaculum rodentium and its human homologue protect from intestinal tumour growth.

Nat Microbiol. 2020-1-27

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