Modulation of DNA damage response by sphingolipid signaling: An interplay that shapes cell fate

dc.contributor.authorFrancis, Marina
dc.contributor.authorAbou Daher, Alaa
dc.contributor.authorAzzam, Patrick
dc.contributor.authorMroueh, Manal
dc.contributor.authorZeidan, Youssef H.
dc.contributor.departmentAnatomy, Cell Biology, and Physiological Sciences
dc.contributor.departmentRadiation Oncology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:36:56Z
dc.date.available2025-01-24T11:36:56Z
dc.date.issued2020
dc.description.abstractAlthough 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.doihttps://doi.org/10.3390/ijms21124481
dc.identifier.eid2-s2.0-85086864532
dc.identifier.pmid32599736
dc.identifier.urihttp://hdl.handle.net/10938/28760
dc.language.isoen
dc.publisherMDPI AG
dc.relation.ispartofInternational Journal of Molecular Sciences
dc.sourceScopus
dc.subjectAtm
dc.subjectDna damage response
dc.subjectDouble strand breaks
dc.subjectIonizing radiation
dc.subjectMetabolic stress
dc.subjectNuclear sphingolipids
dc.subjectOxidative stress
dc.subjectP53
dc.subjectSphingolipids
dc.subjectAnimals
dc.subjectCell differentiation
dc.subjectCell survival
dc.subjectDna damage
dc.subjectDna repair
dc.subjectHumans
dc.subjectRadiation, ionizing
dc.subjectSignal transduction
dc.subjectStress, physiological
dc.subjectAtm protein
dc.subjectCeramidase
dc.subjectCeramide
dc.subjectCeramide 1 phosphate
dc.subjectCeramide glucosyltransferase
dc.subjectCeramide kinase
dc.subjectDouble stranded rna
dc.subjectFatty acid
dc.subjectGalactosylceramide
dc.subjectGlycosphingolipid
dc.subjectPalmitoyl coenzyme a
dc.subjectProtein p53
dc.subjectSphingolipid
dc.subjectSphingomyelin
dc.subjectSphingosine
dc.subjectSphingosine 1 phosphate
dc.subjectTelomerase
dc.subjectAcetylation
dc.subjectAcylation
dc.subjectApoptosis
dc.subjectAtaxia telangiectasia
dc.subjectCatabolism
dc.subjectCell cycle arrest
dc.subjectCell cycle progression
dc.subjectCell death
dc.subjectCell fate
dc.subjectCell growth
dc.subjectCell nucleus membrane
dc.subjectDouble strand break repair
dc.subjectDown regulation
dc.subjectEpigenetic modification
dc.subjectGene mutation
dc.subjectGenetic transcription
dc.subjectHuman
dc.subjectMetabolism
dc.subjectMetabolite
dc.subjectMitosis
dc.subjectNecrosis
dc.subjectNucleocytoplasmic transport
dc.subjectReview
dc.subjectSenescence
dc.subjectSingle strand break repair
dc.subjectAnimal
dc.subjectPhysiological stress
dc.titleModulation of DNA damage response by sphingolipid signaling: An interplay that shapes cell fate
dc.typeReview

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