Modulation of DNA damage response by sphingolipid signaling: An interplay that shapes cell fate
| dc.contributor.author | Francis, Marina | |
| dc.contributor.author | Abou Daher, Alaa | |
| dc.contributor.author | Azzam, Patrick | |
| dc.contributor.author | Mroueh, Manal | |
| dc.contributor.author | Zeidan, Youssef H. | |
| dc.contributor.department | Anatomy, Cell Biology, and Physiological Sciences | |
| dc.contributor.department | Radiation Oncology | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T11:36:56Z | |
| dc.date.available | 2025-01-24T11:36:56Z | |
| dc.date.issued | 2020 | |
| dc.description.abstract | 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. © 2020 by the authors. Licensee MDPI, Basel, Switzerland. | |
| dc.identifier.doi | https://doi.org/10.3390/ijms21124481 | |
| dc.identifier.eid | 2-s2.0-85086864532 | |
| dc.identifier.pmid | 32599736 | |
| dc.identifier.uri | http://hdl.handle.net/10938/28760 | |
| dc.language.iso | en | |
| dc.publisher | MDPI AG | |
| dc.relation.ispartof | International Journal of Molecular Sciences | |
| dc.source | Scopus | |
| dc.subject | Atm | |
| dc.subject | Dna damage response | |
| dc.subject | Double strand breaks | |
| dc.subject | Ionizing radiation | |
| dc.subject | Metabolic stress | |
| dc.subject | Nuclear sphingolipids | |
| dc.subject | Oxidative stress | |
| dc.subject | P53 | |
| dc.subject | Sphingolipids | |
| dc.subject | Animals | |
| dc.subject | Cell differentiation | |
| dc.subject | Cell survival | |
| dc.subject | Dna damage | |
| dc.subject | Dna repair | |
| dc.subject | Humans | |
| dc.subject | Radiation, ionizing | |
| dc.subject | Signal transduction | |
| dc.subject | Stress, physiological | |
| dc.subject | Atm protein | |
| dc.subject | Ceramidase | |
| dc.subject | Ceramide | |
| dc.subject | Ceramide 1 phosphate | |
| dc.subject | Ceramide glucosyltransferase | |
| dc.subject | Ceramide kinase | |
| dc.subject | Double stranded rna | |
| dc.subject | Fatty acid | |
| dc.subject | Galactosylceramide | |
| dc.subject | Glycosphingolipid | |
| dc.subject | Palmitoyl coenzyme a | |
| dc.subject | Protein p53 | |
| dc.subject | Sphingolipid | |
| dc.subject | Sphingomyelin | |
| dc.subject | Sphingosine | |
| dc.subject | Sphingosine 1 phosphate | |
| dc.subject | Telomerase | |
| dc.subject | Acetylation | |
| dc.subject | Acylation | |
| dc.subject | Apoptosis | |
| dc.subject | Ataxia telangiectasia | |
| dc.subject | Catabolism | |
| dc.subject | Cell cycle arrest | |
| dc.subject | Cell cycle progression | |
| dc.subject | Cell death | |
| dc.subject | Cell fate | |
| dc.subject | Cell growth | |
| dc.subject | Cell nucleus membrane | |
| dc.subject | Double strand break repair | |
| dc.subject | Down regulation | |
| dc.subject | Epigenetic modification | |
| dc.subject | Gene mutation | |
| dc.subject | Genetic transcription | |
| dc.subject | Human | |
| dc.subject | Metabolism | |
| dc.subject | Metabolite | |
| dc.subject | Mitosis | |
| dc.subject | Necrosis | |
| dc.subject | Nucleocytoplasmic transport | |
| dc.subject | Review | |
| dc.subject | Senescence | |
| dc.subject | Single strand break repair | |
| dc.subject | Animal | |
| dc.subject | Physiological stress | |
| dc.title | Modulation of DNA damage response by sphingolipid signaling: An interplay that shapes cell fate | |
| dc.type | Review |
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