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肿瘤相关巨噬细胞的转录、表观遗传和代谢重编程

Transcriptional, Epigenetic and Metabolic Programming of Tumor-Associated Macrophages.

作者信息

Larionova Irina, Kazakova Elena, Patysheva Marina, Kzhyshkowska Julia

机构信息

Laboratory of Translational Cellular and Molecular Biomedicine, National Research Tomsk State University, 634050 Tomsk, Russia.

Cancer Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences, 634009 Tomsk, Russia.

出版信息

Cancers (Basel). 2020 May 29;12(6):1411. doi: 10.3390/cancers12061411.

DOI:10.3390/cancers12061411
PMID:32486098
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7352439/
Abstract

Macrophages are key innate immune cells in the tumor microenvironment (TME) that regulate primary tumor growth, vascularization, metastatic spread and tumor response to various types of therapies. The present review highlights the mechanisms of macrophage programming in tumor microenvironments that act on the transcriptional, epigenetic and metabolic levels. We summarize the latest knowledge on the types of transcriptional factors and epigenetic enzymes that control the direction of macrophage functional polarization and their pro- and anti-tumor activities. We also focus on the major types of metabolic programs of macrophages (glycolysis and fatty acid oxidation), and their interaction with cancer cells and complex TME. We have discussed how the regulation of macrophage polarization on the transcriptional, epigenetic and metabolic levels can be used for the efficient therapeutic manipulation of macrophage functions in cancer.

摘要

巨噬细胞是肿瘤微环境(TME)中的关键固有免疫细胞,可调节原发性肿瘤生长、血管生成、转移扩散以及肿瘤对各种治疗的反应。本综述重点介绍了肿瘤微环境中巨噬细胞编程在转录、表观遗传和代谢水平上发挥作用的机制。我们总结了关于控制巨噬细胞功能极化方向及其促肿瘤和抗肿瘤活性的转录因子和表观遗传酶类型的最新知识。我们还关注巨噬细胞的主要代谢程序类型(糖酵解和脂肪酸氧化),以及它们与癌细胞和复杂肿瘤微环境的相互作用。我们讨论了如何在转录、表观遗传和代谢水平上调节巨噬细胞极化,以有效治疗性操控癌症中巨噬细胞的功能。

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Epigenetic Regulation of S100A9 and S100A12 Expression in Monocyte-Macrophage System in Hyperglycemic Conditions.高血糖条件下单核巨噬细胞系统中 S100A9 和 S100A12 表达的表观遗传调控。
Front Immunol. 2020 Jun 2;11:1071. doi: 10.3389/fimmu.2020.01071. eCollection 2020.
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Targeting glutamine metabolism enhances tumor-specific immunity by modulating suppressive myeloid cells.靶向谷氨酰胺代谢通过调节抑制性髓系细胞增强肿瘤特异性免疫。
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Classical Activation of Macrophages Leads to Lipid Droplet Formation Without Fatty Acid Synthesis.
C1Q TPP1巨噬细胞通过SETD8驱动的p53甲基化促进结肠癌进展。
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The epigenetic hallmarks of immune cells in cancer.癌症中免疫细胞的表观遗传特征。
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Anti-Inflammatory Effects of SGLT2 Inhibitors: Focus on Macrophages.钠-葡萄糖协同转运蛋白2抑制剂的抗炎作用:聚焦于巨噬细胞
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Lymphatic-derived oxysterols promote anti-tumor immunity and response to immunotherapy in melanoma.源自淋巴管的氧化甾醇可促进黑色素瘤的抗肿瘤免疫及对免疫疗法的反应。
Nat Commun. 2025 Jan 31;16(1):1217. doi: 10.1038/s41467-025-55969-w.
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Altered AP-1, RUNX and EGR chromatin dynamics drive fibrotic lung disease.AP-1、RUNX和EGR染色质动力学改变驱动肺纤维化疾病。
bioRxiv. 2024 Oct 28:2024.10.23.619858. doi: 10.1101/2024.10.23.619858.
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Targeting of TAMs: can we be more clever than cancer cells?靶向肿瘤相关巨噬细胞:我们能否比癌细胞更聪明?
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J Exp Clin Cancer Res. 2024 Aug 8;43(1):220. doi: 10.1186/s13046-024-03128-2.
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