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Amino Acid Transporters as Targets for Cancer Therapy: Why, Where, When, and How

Amino acids are indispensable for the growth of cancer cells. This includes essential amino acids, the carbon skeleton of which cannot be synthesized, and conditionally essential amino acids, for which the metabolic demands exceed the capacity to synthesize them. Moreover, amino acids are important...

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Detalles Bibliográficos
Autor principal: Bröer, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503255/
https://www.ncbi.nlm.nih.gov/pubmed/32859034
http://dx.doi.org/10.3390/ijms21176156
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author Bröer, Stefan
author_facet Bröer, Stefan
author_sort Bröer, Stefan
collection PubMed
description Amino acids are indispensable for the growth of cancer cells. This includes essential amino acids, the carbon skeleton of which cannot be synthesized, and conditionally essential amino acids, for which the metabolic demands exceed the capacity to synthesize them. Moreover, amino acids are important signaling molecules regulating metabolic pathways, protein translation, autophagy, defense against reactive oxygen species, and many other functions. Blocking uptake of amino acids into cancer cells is therefore a viable strategy to reduce growth. A number of studies have used genome-wide silencing or knock-out approaches, which cover all known amino acid transporters in a large variety of cancer cell lines. In this review, these studies are interrogated together with other databases to identify vulnerabilities with regard to amino acid transport. Several themes emerge, such as synthetic lethality, reduced redundancy, and selective vulnerability, which can be exploited to stop cancer cell growth.
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spelling pubmed-75032552020-09-23 Amino Acid Transporters as Targets for Cancer Therapy: Why, Where, When, and How Bröer, Stefan Int J Mol Sci Review Amino acids are indispensable for the growth of cancer cells. This includes essential amino acids, the carbon skeleton of which cannot be synthesized, and conditionally essential amino acids, for which the metabolic demands exceed the capacity to synthesize them. Moreover, amino acids are important signaling molecules regulating metabolic pathways, protein translation, autophagy, defense against reactive oxygen species, and many other functions. Blocking uptake of amino acids into cancer cells is therefore a viable strategy to reduce growth. A number of studies have used genome-wide silencing or knock-out approaches, which cover all known amino acid transporters in a large variety of cancer cell lines. In this review, these studies are interrogated together with other databases to identify vulnerabilities with regard to amino acid transport. Several themes emerge, such as synthetic lethality, reduced redundancy, and selective vulnerability, which can be exploited to stop cancer cell growth. MDPI 2020-08-26 /pmc/articles/PMC7503255/ /pubmed/32859034 http://dx.doi.org/10.3390/ijms21176156 Text en © 2020 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Bröer, Stefan
Amino Acid Transporters as Targets for Cancer Therapy: Why, Where, When, and How
title Amino Acid Transporters as Targets for Cancer Therapy: Why, Where, When, and How
title_full Amino Acid Transporters as Targets for Cancer Therapy: Why, Where, When, and How
title_fullStr Amino Acid Transporters as Targets for Cancer Therapy: Why, Where, When, and How
title_full_unstemmed Amino Acid Transporters as Targets for Cancer Therapy: Why, Where, When, and How
title_short Amino Acid Transporters as Targets for Cancer Therapy: Why, Where, When, and How
title_sort amino acid transporters as targets for cancer therapy: why, where, when, and how
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503255/
https://www.ncbi.nlm.nih.gov/pubmed/32859034
http://dx.doi.org/10.3390/ijms21176156
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