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肠道微生物群:肝细胞癌耐药性的新兴调节因子。

The gut microbiota: an emerging modulator of drug resistance in hepatocellular carcinoma.

作者信息

Yao Jiali, Ning Beifang, Ding Jin

机构信息

Clinical Cancer Institute, Center for Translational Medicine, Naval Medical University, Shanghai, China.

Department of Gastroenterology, Changzheng Hospital, Naval Medical University, Shanghai, China.

出版信息

Gut Microbes. 2025 Dec;17(1):2473504. doi: 10.1080/19490976.2025.2473504. Epub 2025 Mar 5.


DOI:10.1080/19490976.2025.2473504
PMID:40042184
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11901387/
Abstract

Liver cancer is usually diagnosed at an advanced stage and is the third most common cause of cancer-related death worldwide. In addition to the lack of effective treatment options, resistance to therapeutic drugs is a major clinical challenge. The gut microbiota has recently been recognized as one of the key factors regulating host health. The microbiota and its metabolites can directly or indirectly regulate gene expression in the liver, leading to gut-liver axis dysregulation, which is closely related to liver cancer occurrence and the treatment response. Gut microbiota disturbance may participate in tumor progression and drug resistance through metabolite production, gene transfer, immune regulation, and other mechanisms. However, systematic reviews on the role of the gut microbiota in drug resistance in liver cancer are lacking. Herein, we review the relationships between the gut microbiota and the occurrence and drug resistance of hepatocellular carcinoma, summarize the emerging mechanisms underlying gut microbiota-mediated drug resistance, and propose new personalized treatment options to overcome this resistance.

摘要

肝癌通常在晚期被诊断出来,是全球癌症相关死亡的第三大常见原因。除了缺乏有效的治疗方案外,对治疗药物的耐药性是一个主要的临床挑战。肠道微生物群最近被认为是调节宿主健康的关键因素之一。微生物群及其代谢产物可以直接或间接调节肝脏中的基因表达,导致肠-肝轴失调,这与肝癌的发生和治疗反应密切相关。肠道微生物群紊乱可能通过代谢产物产生、基因转移、免疫调节等机制参与肿瘤进展和耐药性。然而,关于肠道微生物群在肝癌耐药性中作用的系统综述尚缺乏。在此,我们综述了肠道微生物群与肝细胞癌发生和耐药性之间的关系,总结了肠道微生物群介导耐药性的新出现机制,并提出了克服这种耐药性的新的个性化治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48fe/11901387/f5672d67896b/KGMI_A_2473504_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48fe/11901387/1004756f4695/KGMI_A_2473504_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48fe/11901387/f5672d67896b/KGMI_A_2473504_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48fe/11901387/1004756f4695/KGMI_A_2473504_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48fe/11901387/f5672d67896b/KGMI_A_2473504_F0002_OC.jpg

相似文献

[1]
The gut microbiota: an emerging modulator of drug resistance in hepatocellular carcinoma.

Gut Microbes. 2025-12

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
Gut-liver axis-mediated mechanism of liver cancer: A special focus on the role of gut microbiota.

Cancer Sci. 2021-11

[9]
Gut microbial dysbiosis associates hepatocellular carcinoma via the gut-liver axis.

Hepatobiliary Pancreat Dis Int. 2018-11-22

[10]
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Cancer Lett. 2019-6-8

引用本文的文献

[1]
Molecular Mechanisms of Probiotic Action Against Gastrointestinal Cancers.

Int J Mol Sci. 2025-8-14

[2]
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Drug Des Devel Ther. 2025-7-15

[3]
Microbial Metabolite Effects on Vasculogenic Mimicry in Metastatic Cancers.

Cells. 2025-5-30

本文引用的文献

[1]
Nisin lantibiotic prevents NAFLD liver steatosis and mitochondrial oxidative stress following periodontal disease by abrogating oral, gut and liver dysbiosis.

NPJ Biofilms Microbiomes. 2024-1-17

[2]
The microbial metabolite desaminotyrosine enhances T-cell priming and cancer immunotherapy with immune checkpoint inhibitors.

EBioMedicine. 2023-11

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Altered gut microbiome, bile acid composition and metabolome in sarcopenia in liver cirrhosis.

J Cachexia Sarcopenia Muscle. 2023-12

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Medicina (Kaunas). 2023-8-6

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5‑Fluorouracil and capecitabine therapies for the treatment of colorectal cancer (Review).

Oncol Rep. 2023-10

[6]
Escherichia coli Promotes Endothelial to Mesenchymal Transformation of Liver Sinusoidal Endothelial Cells and Exacerbates Nonalcoholic Fatty Liver Disease Via Its Flagellin.

Cell Mol Gastroenterol Hepatol. 2023

[7]
The gut-liver axis and gut microbiota in health and liver disease.

Nat Rev Microbiol. 2023-11

[8]
Dysbiosis of the gut microbiome in elderly patients with hepatocellular carcinoma.

Sci Rep. 2023-5-13

[9]
Fecal levels of SCFA and BCFA during capecitabine in patients with metastatic or unresectable colorectal cancer.

Clin Exp Med. 2023-11

[10]
Foodborne Carbon Dot Exposure Induces Insulin Resistance through Gut Microbiota Dysbiosis and Damaged Intestinal Mucus Layer.

ACS Nano. 2023-3-28

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