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肠道微生物群在肿瘤发生和治疗中的作用。

Role of the gut microbiota in tumorigenesis and treatment.

作者信息

Liu Qingya, Yang Yun, Pan Meng, Yang Fan, Yu Yan, Qian Zhiyong

机构信息

Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, China.

Department of Pharmacy, West China Hospital, Sichuan University, Chengdu, 610041, China.

出版信息

Theranostics. 2024 Mar 17;14(6):2304-2328. doi: 10.7150/thno.91700. eCollection 2024.


DOI:10.7150/thno.91700
PMID:38646653
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11024857/
Abstract

The gut microbiota is a crucial component of the intricate microecosystem within the human body that engages in interactions with the host and influences various physiological processes and pathological conditions. In recent years, the association between dysbiosis of the gut microbiota and tumorigenesis has garnered increasing attention, as it is recognized as a hallmark of cancer within the scientific community. However, only a few microorganisms have been identified as potential drivers of tumorigenesis, and enhancing the molecular understanding of this process has substantial scientific importance and clinical relevance for cancer treatment. In this review, we delineate the impact of the gut microbiota on tumorigenesis and treatment in multiple types of cancer while also analyzing the associated molecular mechanisms. Moreover, we discuss the utility of gut microbiota data in cancer diagnosis and patient stratification. We further outline current research on harnessing microorganisms for cancer treatment while also analyzing the prospects and challenges associated with this approach.

摘要

肠道微生物群是人体复杂微生态系统的关键组成部分,它与宿主相互作用,影响各种生理过程和病理状况。近年来,肠道微生物群失调与肿瘤发生之间的关联越来越受到关注,因为它在科学界被认为是癌症的一个标志。然而,只有少数微生物被确定为肿瘤发生的潜在驱动因素,加强对这一过程的分子理解对癌症治疗具有重大的科学意义和临床相关性。在这篇综述中,我们阐述了肠道微生物群对多种癌症肿瘤发生和治疗的影响,同时分析了相关的分子机制。此外,我们讨论了肠道微生物群数据在癌症诊断和患者分层中的应用。我们进一步概述了目前利用微生物进行癌症治疗的研究,同时分析了这种方法的前景和挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/52382e752ecd/thnov14p2304g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/afcf151fd460/thnov14p2304g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/50c293935c3e/thnov14p2304g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/900eb2c3a4f3/thnov14p2304g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/4decea6db75b/thnov14p2304g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/2ae674a29baa/thnov14p2304g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/4f59c6f6e64a/thnov14p2304g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/52382e752ecd/thnov14p2304g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/afcf151fd460/thnov14p2304g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/50c293935c3e/thnov14p2304g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/900eb2c3a4f3/thnov14p2304g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/4decea6db75b/thnov14p2304g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/2ae674a29baa/thnov14p2304g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/4f59c6f6e64a/thnov14p2304g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b873/11024857/52382e752ecd/thnov14p2304g007.jpg

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本文引用的文献

[1]
Dietary resistant starch supplementation increases gut luminal deoxycholic acid abundance in mice.

Gut Microbes. 2024

[2]
Effect of structural characteristics of resistant starch prepared by various methods on microbial community and fermentative products.

Int J Biol Macromol. 2024-1

[3]
Bacteroides fragilis uses toxins for gut success.

Nat Microbiol. 2024-1

[4]
Multi-kingdom gut microbiota analyses define bacterial-fungal interplay and microbial markers of pan-cancer immunotherapy across cohorts.

Cell Host Microbe. 2023-11-8

[5]
A Novel Cytochrome P450 2E1 Inhibitor Q11 Is Effective on Lung Cancer via Regulation of the Inflammatory Microenvironment.

Adv Sci (Weinh). 2023-12

[6]
Reactive oxygen species and gastric carcinogenesis: The complex interaction between Helicobacter pylori and host.

Helicobacter. 2023-12

[7]
A New Paradigm in the Relationship between Gut Microbiota and Breast Cancer: β-glucuronidase Enzyme Identified as Potential Therapeutic Target.

Pathogens. 2023-8-26

[8]
Biomarkers for immunotherapy of hepatocellular carcinoma.

Nat Rev Clin Oncol. 2023-11

[9]
Dissecting Microbiome-Derived SCFAs in Prostate Cancer: Analyzing Gut Microbiota, Racial Disparities, and Epigenetic Mechanisms.

Cancers (Basel). 2023-8-14

[10]
Gut microbiota-derived short-chain fatty acids promote prostate cancer progression via inducing cancer cell autophagy and M2 macrophage polarization.

Neoplasia. 2023-9

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