| Literature DB >> 32015091 |
Pan Su1, Qiang Wang1, Enguang Bi1, Xingzhe Ma1, Lintao Liu1, Maojie Yang1, Jianfei Qian1, Qing Yi2.
Abstract
Tumor-associated macrophages (TAM) are important tumor-promoting cells. However, the mechanisms underlying how the tumor and its microenvironment reprogram these cells remain elusive. Here we report that lipids play a crucial role in generating TAMs in the tumor microenvironment (TME). Macrophages from both human and murine tumor tissues were enriched with lipids due to increased lipid uptake by macrophages. TAMs expressed elevated levels of the scavenger receptor CD36, accumulated lipids, and used fatty acid oxidation (FAO) instead of glycolysis for energy. High levels of FAO promoted mitochondrial oxidative phosphorylation, production of reactive oxygen species, phosphorylation of JAK1, and dephosphorylation of SHP1, leading to STAT6 activation and transcription of genes that regulate TAM generation and function. These processes were critical for TAM polarization and activity, both in vitro and in vivo. In summary, we highlight the importance of lipid metabolism in the differentiation and function of protumor TAMs in the TME. SIGNIFICANCE: This study highlights the role of lipid metabolism in the differentiation and function of TAMs and suggests targeting TAM fatty acid oxidation as a potential therapeutic modality for human cancers. ©2020 American Association for Cancer Research.Entities:
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Year: 2020 PMID: 32015091 PMCID: PMC7127942 DOI: 10.1158/0008-5472.CAN-19-2994
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701