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本文引用的文献

1
Annual report to the nation on the status of cancer, part 1: National cancer statistics.国家癌症报告:癌症统计数据 1. 全国癌症统计数据概览
Cancer. 2022 Dec 15;128(24):4251-4284. doi: 10.1002/cncr.34479. Epub 2022 Oct 27.
2
Gut-liver axis: Pathophysiological concepts and clinical implications.肠-肝轴:病理生理概念及临床意义。
Cell Metab. 2022 Nov 1;34(11):1700-1718. doi: 10.1016/j.cmet.2022.09.017. Epub 2022 Oct 7.
3
Diet-driven microbial ecology underpins associations between cancer immunotherapy outcomes and the gut microbiome.饮食驱动的微生物生态学是癌症免疫治疗结果与肠道微生物群之间关联的基础。
Nat Med. 2022 Nov;28(11):2344-2352. doi: 10.1038/s41591-022-01965-2. Epub 2022 Sep 22.
4
The association between antibiotic use and outcomes of HCC patients treated with immune checkpoint inhibitors.抗生素使用与免疫检查点抑制剂治疗 HCC 患者结局的关系。
Front Immunol. 2022 Aug 17;13:956533. doi: 10.3389/fimmu.2022.956533. eCollection 2022.
5
Imbalanced gut microbiota fuels hepatocellular carcinoma development by shaping the hepatic inflammatory microenvironment.肠道微生物菌群失衡通过塑造肝脏炎症微环境促进肝癌发展。
Nat Commun. 2022 Jul 8;13(1):3964. doi: 10.1038/s41467-022-31312-5.
6
Changing global epidemiology of liver cancer from 2010 to 2019: NASH is the fastest growing cause of liver cancer.2010 年至 2019 年全球肝癌流行病学变化:NASH 是肝癌增长最快的病因。
Cell Metab. 2022 Jul 5;34(7):969-977.e2. doi: 10.1016/j.cmet.2022.05.003. Epub 2022 Jun 3.
7
Gasdermin D-mediated release of IL-33 from senescent hepatic stellate cells promotes obesity-associated hepatocellular carcinoma.Gasdermin D 介导的衰老肝星状细胞中 IL-33 的释放促进肥胖相关肝细胞癌。
Sci Immunol. 2022 Jun 24;7(72):eabl7209. doi: 10.1126/sciimmunol.abl7209.
8
Gut microbiota and metabolites associate with outcomes of immune checkpoint inhibitor-treated unresectable hepatocellular carcinoma.肠道微生物群和代谢物与免疫检查点抑制剂治疗不可切除肝细胞癌的结果相关。
J Immunother Cancer. 2022 Jun;10(6). doi: 10.1136/jitc-2022-004779.
9
Intratumoral Microbiome of Human Primary Liver Cancer.人原发性肝癌的肿瘤内微生物组。
Hepatol Commun. 2022 Jul;6(7):1741-1752. doi: 10.1002/hep4.1908. Epub 2022 Feb 22.
10
Intrahepatic microbes govern liver immunity by programming NKT cells.肝内微生物通过编程 NKT 细胞来控制肝脏免疫。
J Clin Invest. 2022 Apr 15;132(8). doi: 10.1172/JCI151725.

肠道微生物群与肝癌

The Microbiome and Liver Cancer.

机构信息

From the Gastrointestinal Malignancies Section, Thoracic and GI Malignancies Branch.

NCI CCR Liver Cancer Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD.

出版信息

Cancer J. 2023;29(2):57-60. doi: 10.1097/PPO.0000000000000646.

DOI:10.1097/PPO.0000000000000646
PMID:36957974
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10168020/
Abstract

The gut microbiome and liver are anatomically and functionally connected. The impact of the gut microbiota or microbial metabolites on liver cancer progression via immune cells has been recently revealed across various preclinical models. Commensal gut microbes of liver cancer patients differ from control subjects, and their composition is affected by the etiology of the hepatocellular carcinoma. The gut microbiota represents a potential novel target for intervention as shown in patients with melanoma, but we still lack data in patients with hepatocellular carcinoma. Fecal microbiota transplantation and dietary approaches may improve immunotherapy efficacy, and a couple of clinical trials are ongoing. In liver cancer, the ongoing recognition of interactions between gut microbes and the tumor immune microenvironment provides an exciting therapeutic avenue to complement established immunotherapy.

摘要

肠道微生物群与肝脏在解剖和功能上是相连的。最近在各种临床前模型中发现,肠道微生物群或微生物代谢物通过免疫细胞对肝癌的进展有影响。肝癌患者的肠道共生微生物与对照者不同,其组成受肝细胞癌病因的影响。肠道微生物群代表了一个潜在的新的干预靶点,这在黑色素瘤患者中已经得到了证实,但我们在肝细胞癌患者中仍然缺乏数据。粪便微生物群移植和饮食方法可能会提高免疫疗法的疗效,目前有几项临床试验正在进行。在肝癌中,对肠道微生物群与肿瘤免疫微环境之间相互作用的不断认识为补充现有的免疫疗法提供了一个令人兴奋的治疗途径。