Jia Siyuan, Bode Ann M, Chen Xue, Luo Xiangjian
Hunan Key Laboratory of Oncotarget Gene, Hunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan 410013, PR China; Key Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Cancer Research Institute, School of Basic Medicine, Central South University, Changsha, Hunan 410078, PR China.
The Hormel Institute, University of Minnesota, Austin, MN 55912, USA.
Biochim Biophys Acta Rev Cancer. 2024 Sep;1879(5):189166. doi: 10.1016/j.bbcan.2024.189166. Epub 2024 Aug 5.
Cancer incidence and mortality are increasing and impacting global life expectancy. Metabolic reprogramming in the tumor microenvironment (TME) is intimately related to tumorigenesis, progression, metastasis and drug resistance. Tumor cells drive metabolic reprogramming of other cells in the TME through metabolic induction of cytokines and metabolites, and metabolic substrate competition. Consequently, this boosts tumor cell growth by providing metabolic support and facilitating immunosuppression and angiogenesis. The metabolic interplay in the TME presents potential therapeutic targets. Here, we focus on the metabolic reprogramming of four principal cell subsets in the TME: CAFs, TAMs, TILs and TECs, and their interaction with tumor cells. We also summarize medications and therapies targeting these cells' metabolic pathways, particularly in the context of immune checkpoint blockade therapy.
癌症发病率和死亡率不断上升,影响着全球预期寿命。肿瘤微环境(TME)中的代谢重编程与肿瘤发生、发展、转移和耐药性密切相关。肿瘤细胞通过细胞因子和代谢产物的代谢诱导以及代谢底物竞争,驱动TME中其他细胞的代谢重编程。因此,这通过提供代谢支持、促进免疫抑制和血管生成来促进肿瘤细胞生长。TME中的代谢相互作用提供了潜在的治疗靶点。在这里,我们重点关注TME中四个主要细胞亚群:癌相关成纤维细胞(CAFs)、肿瘤相关巨噬细胞(TAMs)、肿瘤浸润淋巴细胞(TILs)和肿瘤内皮细胞(TECs)的代谢重编程,以及它们与肿瘤细胞的相互作用。我们还总结了针对这些细胞代谢途径的药物和疗法,特别是在免疫检查点阻断疗法的背景下。
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