Targeting SLC1A5 and SLC3A2/SLC7A5 as a Potential Strategy to Strengthen Anti-Tumor Immunity in the Tumor Microenvironment

Front Immunol. 2021 Apr 19:12:624324. doi: 10.3389/fimmu.2021.624324. eCollection 2021.

Abstract

Cancer cells are metabolically vigorous and are superior in the uptake of nutrients and in the release of the tumor microenvironment (TME)-specific metabolites. They create an acidic, hypoxic, and nutrient-depleted TME that makes it difficult for the cytotoxic immune cells to adapt to the metabolically hostile environment. Since a robust metabolism in immune cells is required for optimal anti-tumor effector functions, the challenges caused by the TME result in severe defects in the invasion and destruction of the established tumors. There have been many recent developments in NK and T cell-mediated immunotherapy, such as engineering them to express chimeric antigen receptors (CARs) to enhance tumor-recognition and infiltration. However, to defeat the tumor and overcome the limitations of the TME, it is essential to fortify these novel therapies by improving the metabolism of the immune cells. One potential strategy to enhance the metabolic fitness of immune cells is to upregulate the expression of nutrient transporters, specifically glucose and amino acid transporters. In particular, the amino acid transporters SLC1A5 and SLC7A5 as well as the ancillary subunit SLC3A2, which are required for efficient uptake of glutamine and leucine respectively, could strengthen the metabolic capabilities and effector functions of tumor-directed CAR-NK and T cells. In addition to enabling the influx and efflux of essential amino acids through the plasma membrane and within subcellular compartments such as the lysosome and the mitochondria, accumulating evidence has demonstrated that the amino acid transporters participate in sensing amino acid levels and thereby activate mTORC1, a master metabolic regulator that promotes cell metabolism, and induce the expression of c-Myc, a transcription factor essential for cell growth and proliferation. In this review, we discuss the regulatory pathways of these amino acid transporters and how we can take advantage of these processes to strengthen immunotherapy against cancer.

Keywords: SLC1A5; SLC3A2; SLC7A5; anti-tumor immunity; immunometabolism; natural killer cells; nutrient transporters; tumor microenvironment.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amino Acid Transport System ASC / antagonists & inhibitors*
  • Amino Acid Transport System ASC / metabolism
  • Amino Acids / metabolism*
  • Animals
  • Antineoplastic Agents / therapeutic use*
  • Energy Metabolism / drug effects
  • Fusion Regulatory Protein 1, Heavy Chain / antagonists & inhibitors*
  • Fusion Regulatory Protein 1, Heavy Chain / metabolism
  • Humans
  • Immunotherapy, Adoptive*
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / metabolism
  • Killer Cells, Natural / transplantation
  • Large Neutral Amino Acid-Transporter 1 / drug effects*
  • Large Neutral Amino Acid-Transporter 1 / metabolism
  • Minor Histocompatibility Antigens / metabolism
  • Molecular Targeted Therapy
  • Neoplasms / drug therapy*
  • Neoplasms / immunology
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • Receptors, Chimeric Antigen / genetics
  • Receptors, Chimeric Antigen / metabolism
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism
  • T-Lymphocytes / transplantation
  • Tumor Microenvironment*

Substances

  • Amino Acid Transport System ASC
  • Amino Acids
  • Antineoplastic Agents
  • Fusion Regulatory Protein 1, Heavy Chain
  • Large Neutral Amino Acid-Transporter 1
  • Minor Histocompatibility Antigens
  • Receptors, Chimeric Antigen
  • SLC1A5 protein, human
  • SLC3A2 protein, human
  • SLC7A5 protein, human

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