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Modulation of DNA Damage Response by Sphingolipid Signaling: An Interplay that Shapes Cell Fate

Although once considered as structural components of eukaryotic biological membranes, research in the past few decades hints at a major role of bioactive sphingolipids in mediating an array of physiological processes including cell survival, proliferation, inflammation, senescence, and death. A larg...

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Detalles Bibliográficos
Autores principales: Francis, Marina, Abou Daher, Alaa, Azzam, Patrick, Mroueh, Manal, Zeidan, Youssef H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349968/
https://www.ncbi.nlm.nih.gov/pubmed/32599736
http://dx.doi.org/10.3390/ijms21124481
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author Francis, Marina
Abou Daher, Alaa
Azzam, Patrick
Mroueh, Manal
Zeidan, Youssef H.
author_facet Francis, Marina
Abou Daher, Alaa
Azzam, Patrick
Mroueh, Manal
Zeidan, Youssef H.
author_sort Francis, Marina
collection PubMed
description Although once considered as structural components of eukaryotic biological membranes, research in the past few decades hints at a major role of bioactive sphingolipids in mediating an array of physiological processes including cell survival, proliferation, inflammation, senescence, and death. A large body of evidence points to a fundamental role for the sphingolipid metabolic pathway in modulating the DNA damage response (DDR). The interplay between these two elements of cell signaling determines cell fate when cells are exposed to metabolic stress or ionizing radiation among other genotoxic agents. In this review, we aim to dissect the mediators of the DDR and how these interact with the different sphingolipid metabolites to mount various cellular responses.
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spelling pubmed-73499682020-07-15 Modulation of DNA Damage Response by Sphingolipid Signaling: An Interplay that Shapes Cell Fate Francis, Marina Abou Daher, Alaa Azzam, Patrick Mroueh, Manal Zeidan, Youssef H. Int J Mol Sci Review Although once considered as structural components of eukaryotic biological membranes, research in the past few decades hints at a major role of bioactive sphingolipids in mediating an array of physiological processes including cell survival, proliferation, inflammation, senescence, and death. A large body of evidence points to a fundamental role for the sphingolipid metabolic pathway in modulating the DNA damage response (DDR). The interplay between these two elements of cell signaling determines cell fate when cells are exposed to metabolic stress or ionizing radiation among other genotoxic agents. In this review, we aim to dissect the mediators of the DDR and how these interact with the different sphingolipid metabolites to mount various cellular responses. MDPI 2020-06-24 /pmc/articles/PMC7349968/ /pubmed/32599736 http://dx.doi.org/10.3390/ijms21124481 Text en © 2020 by the authors. 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
Francis, Marina
Abou Daher, Alaa
Azzam, Patrick
Mroueh, Manal
Zeidan, Youssef H.
Modulation of DNA Damage Response by Sphingolipid Signaling: An Interplay that Shapes Cell Fate
title Modulation of DNA Damage Response by Sphingolipid Signaling: An Interplay that Shapes Cell Fate
title_full Modulation of DNA Damage Response by Sphingolipid Signaling: An Interplay that Shapes Cell Fate
title_fullStr Modulation of DNA Damage Response by Sphingolipid Signaling: An Interplay that Shapes Cell Fate
title_full_unstemmed Modulation of DNA Damage Response by Sphingolipid Signaling: An Interplay that Shapes Cell Fate
title_short Modulation of DNA Damage Response by Sphingolipid Signaling: An Interplay that Shapes Cell Fate
title_sort modulation of dna damage response by sphingolipid signaling: an interplay that shapes cell fate
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349968/
https://www.ncbi.nlm.nih.gov/pubmed/32599736
http://dx.doi.org/10.3390/ijms21124481
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