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Mol Oncol. 2020 Sep;14(9):2251-2270. doi: 10.1002/1878-0261.12703. Epub 2020 Jun 13.
2
Intestinal Flora and Disease Mutually Shape the Regional Immune System in the Intestinal Tract.肠道菌群与疾病共同塑造肠道局部免疫系统。
Front Immunol. 2020 Apr 3;11:575. doi: 10.3389/fimmu.2020.00575. eCollection 2020.
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Epstein-Barr virus-encoded miR-BART6-3p inhibits cancer cell proliferation through the LOC553103-STMN1 axis. Epstein-Barr 病毒编码的 miR-BART6-3p 通过 LOC553103-STMN1 轴抑制癌细胞增殖。
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Gossypol induces apoptosis of multiple myeloma cells through the JUN-JNK pathway.棉酚通过JUN-JNK途径诱导多发性骨髓瘤细胞凋亡。
Am J Cancer Res. 2020 Mar 1;10(3):870-883. eCollection 2020.
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N Engl J Med. 2020 Feb 27;382(9):869-871. doi: 10.1056/NEJMcibr1914890.
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Cell Mol Life Sci. 2020 Aug;77(15):2949-2958. doi: 10.1007/s00018-020-03469-z. Epub 2020 Feb 10.
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肿瘤微环境中的代谢串扰调节抗肿瘤免疫抑制和免疫治疗抵抗。

Metabolic crosstalk in the tumor microenvironment regulates antitumor immunosuppression and immunotherapy resisitance.

机构信息

Center for Aging Biomedicine, Key Laboratory of Protein Chemistry and Developmental Biology of Ministry of Education, College of Life Sciences, Hunan Normal University, Changsha, 410081, China.

Department of Stomatology, NHC Key Laboratory of Carcinogenesis, Xiangya Hospital, Central South University, Changsha, 410078, China.

出版信息

Cell Mol Life Sci. 2021 Jan;78(1):173-193. doi: 10.1007/s00018-020-03581-0. Epub 2020 Jul 11.

DOI:10.1007/s00018-020-03581-0
PMID:32654036
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11072448/
Abstract

The successful treatment of human cancers by immunotherapy has been made possible by breakthroughs in the discovery of immune checkpoint regulators, including CTLA-4 and PD-1/PD-L1. However, the immunosuppressive effect of the tumor microenvironment still represents an important bottleneck that limits the success of immunotherapeutic approaches. The tumor microenvironment influences the metabolic crosstalk between tumor cells and tumor-infiltrating immune cells, creating competition for the utilization of nutrients and promoting immunosuppression. In addition, tumor-derived metabolites regulate the activation and effector function of immune cells through a variety of mechanisms; in turn, the metabolites and other factors secreted by immune cells can also become accomplices to cancer development. Immune-metabolic checkpoint regulation is an emerging concept that is being studied with the aim of restoring the immune response in the tumor microenvironment. In this review, we summarize the metabolic reprogramming of various cell types present in the tumor microenvironment, with a focus on the interaction between the metabolic pathways of these cells and antitumor immunosuppression. We also discuss the main metabolic checkpoints that could provide new means of enhancing antitumor immunotherapy.

摘要

免疫疗法成功治疗人类癌症是由于免疫检查点调节剂的发现取得了突破,包括 CTLA-4 和 PD-1/PD-L1。然而,肿瘤微环境的免疫抑制作用仍然是限制免疫治疗方法成功的一个重要瓶颈。肿瘤微环境影响肿瘤细胞和肿瘤浸润免疫细胞之间的代谢串扰,造成对营养物质利用的竞争,并促进免疫抑制。此外,肿瘤衍生的代谢物通过多种机制调节免疫细胞的激活和效应功能;反过来,免疫细胞分泌的代谢物和其他因子也可能成为癌症发展的帮凶。免疫代谢检查点调节是一个正在研究的新兴概念,旨在恢复肿瘤微环境中的免疫反应。在这篇综述中,我们总结了肿瘤微环境中各种细胞类型的代谢重编程,重点讨论了这些细胞的代谢途径与抗肿瘤免疫抑制之间的相互作用。我们还讨论了可能为增强抗肿瘤免疫治疗提供新方法的主要代谢检查点。