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Obesity Shapes Metabolism in the Tumor Microenvironment to Suppress Anti-Tumor Immunity
Author(s) -
Alison E. Ringel,
Jefte M. Drijvers,
Gregory J. Baker,
Alessia Catozzi,
Juan Carlos GarcíaCañaveras,
Brandon M. Gassaway,
Brian C. Miller,
Vikram R. Juneja,
Thao H. Nguyen,
Shakchhi Joshi,
Cong-Hui Yao,
Haejin Yoon,
Peter T. Sage,
Martin W. LaFleur,
Justin D. Trombley,
Connor A. Jacobson,
Zoltan Maliga,
Steven P. Gygi,
Peter K. Sorger,
Joshua D. Rabinowitz,
Arlene H. Sharpe,
Marcia C. Haigis
Publication year - 2020
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2020.11.009
Subject(s) - tumor microenvironment , biology , cd8 , cancer research , adipose tissue , cytotoxic t cell , immunity , immune system , immunotherapy , tumor progression , cancer , immunology , endocrinology , biochemistry , genetics , in vitro
Obesity is a major cancer risk factor, but how differences in systemic metabolism change the tumor microenvironment (TME) and impact anti-tumor immunity is not understood. Here, we demonstrate that high-fat diet (HFD)-induced obesity impairs CD8 + T cell function in the murine TME, accelerating tumor growth. We generate a single-cell resolution atlas of cellular metabolism in the TME, detailing how it changes with diet-induced obesity. We find that tumor and CD8 + T cells display distinct metabolic adaptations to obesity. Tumor cells increase fat uptake with HFD, whereas tumor-infiltrating CD8 + T cells do not. These differential adaptations lead to altered fatty acid partitioning in HFD tumors, impairing CD8 + T cell infiltration and function. Blocking metabolic reprogramming by tumor cells in obese mice improves anti-tumor immunity. Analysis of human cancers reveals similar transcriptional changes in CD8 + T cell markers, suggesting interventions that exploit metabolism to improve cancer immunotherapy.

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