Novel strategies to improve tumour therapy by targeting the proteins MCT1, MCT4 and LAT1

Eur J Med Chem. 2021 Dec 15:226:113806. doi: 10.1016/j.ejmech.2021.113806. Epub 2021 Aug 26.

Abstract

Poor selectivity, potential systemic toxicity and drug resistance are the main challenges associated with chemotherapeutic drugs. MCT1 and MCT4 and LAT1 play vital roles in tumour metabolism and growth by taking up nutrients and are thus potential targets for tumour therapy. An increasing number of studies have shown the feasibility of including these transporters as components of tumour-targeting therapy. Here, we summarize the recent progress in MCT1-, MCT4-and LAT1-based therapeutic strategies. First, protein structures, expression, relationships with cancer, and substrate characteristics are introduced. Then, different drug targeting and delivery strategies using these proteins have been reviewed, including designing protein inhibitors, prodrugs and nanoparticles. Finally, a dual targeted strategy is discussed because these proteins exert a synergistic effect on tumour proliferation. This article concentrates on tumour treatments targeting MCT1, MCT4 and LAT1 and delivery techniques for improving the antitumour effect. These innovative tactics represent current state-of-the-art developments in transporter-based antitumour drugs.

Keywords: 4; Mono-carboxylate transporter1; Tumour therapy; l-type amino acid transporter 1.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Cell Proliferation / drug effects
  • Drug Screening Assays, Antitumor
  • Humans
  • Large Neutral Amino Acid-Transporter 1 / metabolism*
  • Molecular Structure
  • Monocarboxylic Acid Transporters / antagonists & inhibitors*
  • Monocarboxylic Acid Transporters / metabolism
  • Muscle Proteins / antagonists & inhibitors*
  • Muscle Proteins / metabolism
  • Neoplasms / drug therapy*
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • Symporters / antagonists & inhibitors*
  • Symporters / metabolism

Substances

  • Antineoplastic Agents
  • Large Neutral Amino Acid-Transporter 1
  • Monocarboxylic Acid Transporters
  • Muscle Proteins
  • SLC16A4 protein, human
  • SLC7A5 protein, human
  • Symporters
  • monocarboxylate transport protein 1