Targeting amino acid metabolism in cancer.
Amino acid metabolism
Arginine
Asparagine
Cancer
Cysteine
Methionine
Targeted therapy
Journal
International review of cell and molecular biology
ISSN: 1937-6448
Titre abrégé: Int Rev Cell Mol Biol
Pays: Netherlands
ID NLM: 101475846
Informations de publication
Date de publication:
2022
2022
Historique:
entrez:
25
10
2022
pubmed:
26
10
2022
medline:
28
10
2022
Statut:
ppublish
Résumé
Metabolic rewiring is a characteristic hallmark of cancer cells. This phenomenon sustains uncontrolled proliferation and resistance to apoptosis by increasing nutrients and energy supply. However, reprogramming comes together with vulnerabilities that can be used against tumor and can be applied in targeted therapy. In the last years, the genetic background of tumors has been identified thoroughly and new therapies targeting those mutations tested. Nevertheless, we propose that targeting the phenotype of cancer cells could be another way of treatment aiming to avoid drug resistance and non-responsiveness of cancer patients. Amino acid metabolism is part of the altered processes in cancer cells. Amino acids are building blocks and also sensors of signaling pathways regulating main biological processes. In this comprehensive review, we described four amino acids (asparagine, arginine, methionine, and cysteine) which have been actively investigated as potential targets for anti-tumor therapy. Asparagine depletion is successfully used for decades in the treatment of acute lymphoblastic leukemia and there is a strong implication to apply it to other types of tumors. Arginine auxotrophic tumors are great candidates for arginine-starvation therapy. Higher requirement for essential amino acids such as methionine and cysteine point out promising targetable weaknesses of cancer cells.
Identifiants
pubmed: 36283767
pii: S1937-6448(22)00109-5
doi: 10.1016/bs.ircmb.2022.08.001
pii:
doi:
Substances chimiques
Asparagine
7006-34-0
Cysteine
K848JZ4886
Amino Acids
0
Arginine
94ZLA3W45F
Methionine
AE28F7PNPL
Types de publication
Review
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
37-79Informations de copyright
Copyright © 2022 Elsevier Inc. All rights reserved.