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肝癌中的肿瘤相关巨噬细胞:是敌是友?

Tumor-Associated Macrophages in Hepatocellular Carcinoma: Friend or Foe?

机构信息

Department of Pharmacy, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital, Wuhu, China.

Key Laboratory of Non-coding RNA Transformation Research of Anhui Higher Education Institution, Wuhu, China.

出版信息

Gut Liver. 2021 Jul 15;15(4):500-516. doi: 10.5009/gnl20223.


DOI:10.5009/gnl20223
PMID:33087588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8283292/
Abstract

Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide, and it has diverse etiologies with multiple mechanisms. The diagnosis of HCC typically occurs at advanced stages when there are limited therapeutic options. Hepatocarcinogenesis is considered a multistep process, and hepatic macrophages play a critical role in the inflammatory process leading to HCC. Emerging evidence has shown that tumor-associated macrophages (TAMs) are crucial components defining the HCC immune microenvironment and represent an appealing option for disrupting the formation and development of HCC. In this review, we summarize the current knowledge of the polarization and function of TAMs in the pathogenesis of HCC, as well as the mechanisms underlying TAM-related anti-HCC therapies. Eventually, novel insights into these important aspects of TAMs and their roles in the HCC microenvironment might lead to promising TAM-focused therapeutic strategies for HCC.

摘要

肝细胞癌 (HCC) 是全球最常见的恶性肿瘤之一,其病因多样,发病机制复杂。HCC 的诊断通常发生在晚期,此时治疗选择有限。肝癌发生被认为是一个多步骤的过程,肝巨噬细胞在导致 HCC 的炎症过程中起着关键作用。新出现的证据表明,肿瘤相关巨噬细胞 (TAMs) 是定义 HCC 免疫微环境的关键组成部分,是破坏 HCC 形成和发展的有吸引力的选择。在这篇综述中,我们总结了 TAMs 在 HCC 发病机制中的极化和功能的最新知识,以及与 TAMs 相关的抗 HCC 治疗的机制。最终,对 TAMs 这些重要方面的新认识及其在 HCC 微环境中的作用可能会为 HCC 带来有前景的以 TAMs 为重点的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51c8/8283292/dd2eab04cfad/gnl-15-4-500-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51c8/8283292/9b1152622d13/gnl-15-4-500-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51c8/8283292/142e836314a6/gnl-15-4-500-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51c8/8283292/917c98bb8850/gnl-15-4-500-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51c8/8283292/dd2eab04cfad/gnl-15-4-500-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51c8/8283292/9b1152622d13/gnl-15-4-500-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51c8/8283292/142e836314a6/gnl-15-4-500-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51c8/8283292/917c98bb8850/gnl-15-4-500-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51c8/8283292/dd2eab04cfad/gnl-15-4-500-f4.jpg

相似文献

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Tumor-Associated Macrophages in Hepatocellular Carcinoma: Friend or Foe?

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[2]
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[3]
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Int J Mol Sci. 2024-12-7

[4]
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[5]
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[6]
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[7]
[A risk scoring model based on M2 macrophage-related genes for predicting prognosis of HBV-related hepatocellular carcinoma].

Nan Fang Yi Ke Da Xue Xue Bao. 2024-5-20

[8]
Construction of a Prognostic Model for Hepatocellular Carcinoma Based on Macrophage Polarization-Related Genes.

J Hepatocell Carcinoma. 2024-5-11

[9]
LncRNA MEG3 Reduces the Ratio of M2/M1 Macrophages Through the HuR/CCL5 Axis in Hepatocellular Carcinoma.

J Hepatocell Carcinoma. 2024-3-11

[10]
Knockdown of liver cancer cell-secreted exosomal PSMA5 controls macrophage polarization to restrain cancer progression by blocking JAK2/STAT3 signaling.

Immun Inflamm Dis. 2024-2

本文引用的文献

[1]
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