4.6 Review

ASCT2 and LAT1 Contribution to the Hallmarks of Cancer: From a Molecular Perspective to Clinical Translation

Journal

CANCERS
Volume 13, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/cancers13020203

Keywords

alanine; serine; cysteine transporter 2; L-type amino acid transporter 1; hallmarks of cancer; clinical significance

Categories

Funding

  1. European Regional Development Fund (ERDF) through the Northern Region Operational Program (NORTE2020) [NORTE-01-0247-FEDER-033399]
  2. Fundacao para a Ciencia e Tecnologia (FCT) [SFRH/BPD/114803/2016]
  3. European Social Funds (ESF)
  4. MCTES under the Human Strategic Reference Framework (POCH)
  5. Fundação para a Ciência e a Tecnologia [SFRH/BPD/114803/2016] Funding Source: FCT

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ASCT2 and LAT1 play crucial roles in cancer by impacting cell death resistance, proliferative signaling, cellular energetics regulation, angiogenesis, invasion, and metastasis. They are considered prognostic factors in various cancer types and potential therapeutic targets. Efforts have been made to develop inhibitors for these transporters, with JHP203 being the only compound in a Phase 1 clinical trial at present. Developing and testing novel inhibitors for ASCT2 and LAT1 could significantly improve cancer prognosis.
Simple Summary ASCT2 and LAT1 are amino acid transporters whose impact in cancer has been explored throughout the years. They have been associated with most currently accepted hallmarks of cancer, thus the aim of this review is to report the impact of these transporters in this disease, as well as their clinical significance and applications. ASCT2 and LAT1 have been identified as prognostic factors and potentially as therapeutic targets. In conclusion, the study and development of new inhibitors for these amino acid transporters constitutes a promising approach towards the improvement of cancer treatment and prognosis. The role of the amino acid transporters ASCT2 and LAT1 in cancer has been explored throughout the years. In this review, we report their impact on the hallmarks of cancer, as well as their clinical significance. Overall, both proteins have been associated with cell death resistance through dysregulation of caspases and sustainment of proliferative signaling through mTOR activation. Furthermore, ASCT2 appears to play an important role in cellular energetics regulation, whereas LAT1 expression is associated with angiogenesis and invasion and metastasis activation. The molecular impact of these proteins on the hallmarks of cancer translates into various clinical applications and both transporters have been identified as prognostic factors in many types of cancer. Concerning their role as therapeutic targets, efforts have been undertaken to synthesize competitive or irreversible ASCT2 and LAT1 inhibitors. However, JHP203, a selective inhibitor of the latter, is, to the best of our knowledge, the only compound included in a Phase 1 clinical trial. In conclusion, considering the usefulness of ASCT2 and LAT1 in a variety of cancer-related pathways and cancer therapy/diagnosis, the development and testing of novel inhibitors for these transporters that could be evaluated in clinical trials represents a promising approach to cancer prognosis improvement.

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