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Cysteine as a Carbon Source, a Hot Spot in Cancer Cells Survival

Cancer cells undergo a metabolic rewiring in order to fulfill the energy and biomass requirements. Cysteine is a pivotal organic compound that contributes for cancer metabolic remodeling at three different levels: (1) in redox control, free or as a component of glutathione; (2) in ATP production, vi...

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Autor principal: Serpa, Jacinta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344258/
https://www.ncbi.nlm.nih.gov/pubmed/32714858
http://dx.doi.org/10.3389/fonc.2020.00947
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author Serpa, Jacinta
author_facet Serpa, Jacinta
author_sort Serpa, Jacinta
collection PubMed
description Cancer cells undergo a metabolic rewiring in order to fulfill the energy and biomass requirements. Cysteine is a pivotal organic compound that contributes for cancer metabolic remodeling at three different levels: (1) in redox control, free or as a component of glutathione; (2) in ATP production, via hydrogen sulfide (H(2)S) production, serving as a donor to electron transport chain (ETC), and (3) as a carbon source for biomass and energy production. In the present review, emphasis will be given to the role of cysteine as a carbon source, focusing on the metabolic reliance on cysteine, benefiting the metabolic fitness and survival of cancer cells. Therefore, the interplay between cysteine metabolism and other metabolic pathways, as well as the regulation of cysteine metabolism related enzymes and transporters, will be also addressed. Finally, the usefulness of cysteine metabolic route as a target in cancer treatment will be highlighted.
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spelling pubmed-73442582020-07-25 Cysteine as a Carbon Source, a Hot Spot in Cancer Cells Survival Serpa, Jacinta Front Oncol Oncology Cancer cells undergo a metabolic rewiring in order to fulfill the energy and biomass requirements. Cysteine is a pivotal organic compound that contributes for cancer metabolic remodeling at three different levels: (1) in redox control, free or as a component of glutathione; (2) in ATP production, via hydrogen sulfide (H(2)S) production, serving as a donor to electron transport chain (ETC), and (3) as a carbon source for biomass and energy production. In the present review, emphasis will be given to the role of cysteine as a carbon source, focusing on the metabolic reliance on cysteine, benefiting the metabolic fitness and survival of cancer cells. Therefore, the interplay between cysteine metabolism and other metabolic pathways, as well as the regulation of cysteine metabolism related enzymes and transporters, will be also addressed. Finally, the usefulness of cysteine metabolic route as a target in cancer treatment will be highlighted. Frontiers Media S.A. 2020-06-23 /pmc/articles/PMC7344258/ /pubmed/32714858 http://dx.doi.org/10.3389/fonc.2020.00947 Text en Copyright © 2020 Serpa. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Serpa, Jacinta
Cysteine as a Carbon Source, a Hot Spot in Cancer Cells Survival
title Cysteine as a Carbon Source, a Hot Spot in Cancer Cells Survival
title_full Cysteine as a Carbon Source, a Hot Spot in Cancer Cells Survival
title_fullStr Cysteine as a Carbon Source, a Hot Spot in Cancer Cells Survival
title_full_unstemmed Cysteine as a Carbon Source, a Hot Spot in Cancer Cells Survival
title_short Cysteine as a Carbon Source, a Hot Spot in Cancer Cells Survival
title_sort cysteine as a carbon source, a hot spot in cancer cells survival
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344258/
https://www.ncbi.nlm.nih.gov/pubmed/32714858
http://dx.doi.org/10.3389/fonc.2020.00947
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