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肿瘤代谢物2-羟基戊二酸调节抗肿瘤免疫。

Oncometabolite 2-hydroxyglutarate regulates anti-tumor immunity.

作者信息

Cai Mengyuan, Zhao Jianyi, Ding Qiang, Wei Jifu

机构信息

Department of Pharmacy, The Affiliated Cancer Hospital of Nanjing Medical University, Jiangsu Cancer Hospital, Jiangsu Institute of Cancer Research, Nanjing, China.

Jiangsu Breast Disease Center, The First Affiliated Hospital with Nanjing Medical University, Nanjing, China.

出版信息

Heliyon. 2024 Jan 10;10(2):e24454. doi: 10.1016/j.heliyon.2024.e24454. eCollection 2024 Jan 30.

DOI:10.1016/j.heliyon.2024.e24454
PMID:38293535
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10826830/
Abstract

"Oncometabolite" 2-hydroxyglutarate (2-HG) is an aberrant metabolite found in tumor cells, exerting a pivotal influence on tumor progression. Recent studies have unveiled its impact on the proliferation, activation, and differentiation of anti-tumor T cells. Moreover, 2-HG regulates the function of innate immune components, including macrophages, dendritic cells, natural killer cells, and the complement system. Elevated levels of 2-HG hinder α-KG-dependent dioxygenases (α-KGDDs), contributing to tumorigenesis by disrupting epigenetic regulation, genome integrity, hypoxia-inducible factors (HIF) signaling, and cellular metabolism. The chiral molecular structure of 2-HG produces two enantiomers: D-2-HG and L-2-HG, each with distinct origins and biological functions. Efforts to inhibit D-2-HG and leverage the potential of L-2-HG have demonstrated efficacy in cancer immunotherapy. This review delves into the metabolism, biological functions, and impacts on the tumor immune microenvironment (TIME) of 2-HG, providing a comprehensive exploration of the intricate relationship between 2-HG and antitumor immunity. Additionally, we examine the potential clinical applications of targeted therapy for 2-HG, highlighting recent breakthroughs as well as the existing challenges.

摘要

“肿瘤代谢物”2-羟基戊二酸(2-HG)是一种在肿瘤细胞中发现的异常代谢物,对肿瘤进展具有关键影响。最近的研究揭示了其对抗肿瘤T细胞增殖、活化和分化的影响。此外,2-HG调节先天性免疫成分的功能,包括巨噬细胞、树突状细胞、自然杀伤细胞和补体系统。2-HG水平升高会阻碍α-酮戊二酸依赖性双加氧酶(α-KGDDs),通过破坏表观遗传调控、基因组完整性、缺氧诱导因子(HIF)信号传导和细胞代谢促进肿瘤发生。2-HG的手性分子结构产生两种对映体:D-2-HG和L-2-HG,每种对映体都有不同的来源和生物学功能。抑制D-2-HG并利用L-2-HG的潜力的努力已在癌症免疫治疗中显示出疗效。本综述深入探讨了2-HG的代谢、生物学功能及其对肿瘤免疫微环境(TIME)的影响,全面探索了2-HG与抗肿瘤免疫之间的复杂关系。此外,我们研究了针对2-HG的靶向治疗的潜在临床应用,突出了最近的突破以及现有挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7342/10826830/7c8cb286dceb/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7342/10826830/b26c4d0dda32/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7342/10826830/331c16c1562d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7342/10826830/7c8cb286dceb/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7342/10826830/b26c4d0dda32/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7342/10826830/331c16c1562d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7342/10826830/7c8cb286dceb/gr3.jpg

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