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免疫代谢重编程的分子机制:癌症进展过程中的风向变化。

Molecular Mechanisms Underpinning Immunometabolic Reprogramming: How the Wind Changes during Cancer Progression.

机构信息

Department of Biotechnological and Applied Clinical Sciences (DISCAB), University of L'Aquila, Via Vetoio, Coppito 2, 67100 L'Aquila, Italy.

出版信息

Genes (Basel). 2023 Oct 17;14(10):1953. doi: 10.3390/genes14101953.

DOI:10.3390/genes14101953
PMID:37895302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10606647/
Abstract

Metabolism and the immunological state are intimately intertwined, as defense responses are bioenergetically expensive. Metabolic homeostasis is a key requirement for the proper function of immune cell subsets, and the perturbation of the immune-metabolic balance is a recurrent event in many human diseases, including cancer, due to nutrient fluctuation, hypoxia and additional metabolic changes occurring in the tumor microenvironment (TME). Although much remains to be understood in the field of immunometabolism, here, we report the current knowledge on both physiological and cancer-associated metabolic profiles of immune cells, and the main molecular circuits involved in their regulation, highlighting similarities and differences, and emphasizing immune metabolic liabilities that could be exploited in cancer therapy to overcome immune resistance.

摘要

代谢和免疫状态密切相关,因为防御反应是非常耗能的。代谢稳态是免疫细胞亚群正常功能的关键要求,而免疫代谢平衡的破坏是许多人类疾病(包括癌症)的常见事件,这是由于肿瘤微环境(TME)中发生的营养波动、缺氧和其他代谢变化。尽管在免疫代谢领域还有很多需要了解的地方,但在这里,我们报告了关于免疫细胞的生理和与癌症相关的代谢特征的最新知识,以及它们调节的主要分子途径,突出了相似性和差异性,并强调了可能在癌症治疗中被利用以克服免疫抵抗的免疫代谢缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45d0/10606647/283e69966aab/genes-14-01953-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45d0/10606647/283e69966aab/genes-14-01953-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45d0/10606647/283e69966aab/genes-14-01953-g001.jpg

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本文引用的文献

1
High co-expression of immune checkpoint receptors PD-1, CTLA-4, LAG-3, TIM-3, and TIGIT on tumor-infiltrating lymphocytes in early-stage breast cancer.早期乳腺癌肿瘤浸润淋巴细胞中免疫检查点受体 PD-1、CTLA-4、LAG-3、TIM-3 和 TIGIT 的高共表达。
World J Surg Oncol. 2022 Oct 21;20(1):349. doi: 10.1186/s12957-022-02810-z.
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Visualizing inflammation with an M1 macrophage selective probe via GLUT1 as the gating target.通过葡萄糖转运蛋白 1(GLUT1)作为门控靶点,利用 M1 巨噬细胞选择性探针可视化炎症。
Nat Commun. 2022 Oct 10;13(1):5974. doi: 10.1038/s41467-022-33526-z.
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The requirement for mitochondrial respiration in cancer varies with disease stage.
癌症中线粒体呼吸的需求随疾病阶段而异。
PLoS Biol. 2022 Sep 23;20(9):e3001800. doi: 10.1371/journal.pbio.3001800. eCollection 2022 Sep.
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Knock-out of 5-lipoxygenase in overexpressing tumor cells-consequences on gene expression and cellular function.过表达肿瘤细胞中 5-脂氧合酶的敲除-对基因表达和细胞功能的影响。
Cancer Gene Ther. 2023 Jan;30(1):108-123. doi: 10.1038/s41417-022-00531-9. Epub 2022 Sep 16.
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Metabolic plasticity and regulation of T cell exhaustion.T 细胞耗竭的代谢可塑性和调控。
Immunology. 2022 Dec;167(4):482-494. doi: 10.1111/imm.13575. Epub 2022 Sep 30.
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NF-κB: blending metabolism, immunity, and inflammation.NF-κB:融合代谢、免疫和炎症。
Trends Immunol. 2022 Sep;43(9):757-775. doi: 10.1016/j.it.2022.07.004. Epub 2022 Aug 11.
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PD-L1 regulates cell proliferation and apoptosis in acute myeloid leukemia by activating PI3K-AKT signaling pathway.PD-L1 通过激活 PI3K-AKT 信号通路调节急性髓系白血病细胞的增殖和凋亡。
Sci Rep. 2022 Jul 6;12(1):11444. doi: 10.1038/s41598-022-15020-0.
8
Glutamine Is Required for M1-like Polarization of Macrophages in Response to Mycobacterium tuberculosis Infection.谷氨酰胺对于结核分枝杆菌感染诱导的巨噬细胞 M1 样极化是必需的。
mBio. 2022 Aug 30;13(4):e0127422. doi: 10.1128/mbio.01274-22. Epub 2022 Jun 28.
9
Fumarate suppresses B-cell activation and function through direct inactivation of LYN.富马酸盐通过直接使LYN失活来抑制B细胞的激活和功能。
Nat Chem Biol. 2022 Sep;18(9):954-962. doi: 10.1038/s41589-022-01052-0. Epub 2022 Jun 16.
10
Mechanisms of induction of regulatory B cells in the tumour microenvironment and their contribution to immunosuppression and pro-tumour responses.肿瘤微环境中调节性 B 细胞的诱导机制及其对免疫抑制和促肿瘤反应的贡献。
Clin Exp Immunol. 2022 Jul 22;209(1):33-45. doi: 10.1093/cei/uxac029.