Amino acid metabolism reprogramming: shedding new light on T cell anti-tumor immunity

J Exp Clin Cancer Res. 2023 Nov 3;42(1):291. doi: 10.1186/s13046-023-02845-4.

Abstract

Metabolic reprogramming of amino acids has been increasingly recognized to initiate and fuel tumorigenesis and survival. Therefore, there is emerging interest in the application of amino acid metabolic strategies in antitumor therapy. Tremendous efforts have been made to develop amino acid metabolic node interventions such as amino acid antagonists and targeting amino acid transporters, key enzymes of amino acid metabolism, and common downstream pathways of amino acid metabolism. In addition to playing an essential role in sustaining tumor growth, new technologies and studies has revealed amino acid metabolic reprograming to have wide implications in the regulation of antitumor immune responses. Specifically, extensive crosstalk between amino acid metabolism and T cell immunity has been reported. Tumor cells can inhibit T cell immunity by depleting amino acids in the microenvironment through nutrient competition, and toxic metabolites of amino acids can also inhibit T cell function. In addition, amino acids can interfere with T cells by regulating glucose and lipid metabolism. This crucial crosstalk inspires the exploitation of novel strategies of immunotherapy enhancement and combination, owing to the unprecedented benefits of immunotherapy and the limited population it can benefit. Herein, we review recent findings related to the crosstalk between amino acid metabolism and T cell immunity. We also describe possible approaches to intervene in amino acid metabolic pathways by targeting various signaling nodes. Novel efforts to combine with and unleash potential immunotherapy are also discussed. Hopefully, some strategies that take the lead in the pipeline may soon be used for the common good.

Keywords: Amino acid; Immunotherapy; Metabolism reprogramming; T cell; Tumor microenvironment.

Publication types

  • Review

MeSH terms

  • Amino Acids
  • Energy Metabolism
  • Humans
  • Immunotherapy
  • Neoplasms* / pathology
  • T-Lymphocytes*
  • Tumor Microenvironment

Substances

  • Amino Acids