Circadian clock, cancer, and chemotherapy

dc.contributor.authorSancar, Aziz
dc.contributor.authorLindsey-Boltz, Laura A.
dc.contributor.authorGaddameedhi, Shobhan
dc.contributor.authorSelby, Christopher P.
dc.contributor.authorYe, Rui
dc.contributor.authorChiou, Yi Ying
dc.contributor.authorKemp, Michael G.
dc.date.accessioned2025-10-29T12:07:59Z
dc.date.issued2015
dc.departmentGebze Teknik Üniversitesi
dc.description.abstractThe circadian clock is a global regulatory system that interfaces with most other regulatory systems and pathways in mammalian organisms. Investigations of the circadian clock-DNA damage response connections have revealed that nucleotide excision repair, DNA damage checkpoints, and apoptosis are appreciably influenced by the clock. Although several epidemiological studies in humans and a limited number of genetic studies in mouse model systems have indicated that clock disruption may predispose mammals to cancer, well-controlled genetic studies in mice have not supported the commonly held view that circadian clock disruption is a cancer risk factor. In fact, in the appropriate genetic background, clock disruption may instead aid in cancer regression by promoting intrinsic and extrinsic apoptosis. Finally, the clock may affect the efficacy of cancer treatment (chronochemotherapy) by modulating the pharmacokinetics and pharmacodynamics of chemotherapeutic drugs as well as the activity of the DNA repair enzymes that repair the DNA damage caused by anticancer drugs. © 2015 Elsevier B.V., All rights reserved.
dc.identifier.doi10.1021/bi5007354
dc.identifier.endpage123
dc.identifier.issn1520-4995
dc.identifier.issn0006-2960
dc.identifier.issue2
dc.identifier.pmid25302769
dc.identifier.scopus2-s2.0-84922448694
dc.identifier.scopusqualityQ3
dc.identifier.startpage110
dc.identifier.urihttps://doi.org/10.1021/bi5007354
dc.identifier.urihttps://hdl.handle.net/20.500.14854/14238
dc.identifier.volume54
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherAmerican Chemical Society service@acs.org
dc.relation.ispartofBiochemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_Scopus_20251020
dc.subjectCell death
dc.subjectChemotherapy
dc.subjectDiseases
dc.subjectDNA
dc.subjectGenetic engineering
dc.subjectMammals
dc.subjectRepair
dc.subjectChemotherapeutic drugs
dc.subjectDNA damage response
dc.subjectDNA-repair enzymes
dc.subjectEpidemiological studies
dc.subjectGenetic backgrounds
dc.subjectNucleotide excision repair
dc.subjectPharmacokinetics and pharmacodynamics
dc.subjectRegulatory systems
dc.subjectClocks
dc.subjectantineoplastic agent
dc.subjectATR protein
dc.subjectcheckpoint kinase 1
dc.subjectexcision repair cross complementing protein 1
dc.subjectprotein BMAL1
dc.subjectprotein p53
dc.subjectprotein p63
dc.subjectprotein p73
dc.subjectprotein timeless
dc.subjecttranscription factor CLOCK
dc.subjecttranscription factor IIH
dc.subjectxeroderma pigmentosum group A protein
dc.subjectxeroderma pigmentosum group C protein
dc.subjectDNA ligase
dc.subjectapoptosis
dc.subjectArticle
dc.subjectcancer chemotherapy
dc.subjectcancer growth
dc.subjectcancer risk
dc.subjectcarcinogenesis
dc.subjectchronotherapy
dc.subjectcircadian rhythm
dc.subjectdirect DNA repair
dc.subjectdisease association
dc.subjectDNA damage
dc.subjectDNA damage checkpoint
dc.subjectDNA repair
dc.subjectDNA replication
dc.subjectenzyme phosphorylation
dc.subjectexcision repair
dc.subjectG1 phase cell cycle checkpoint
dc.subjectG2 phase cell cycle checkpoint
dc.subjectgene repression
dc.subjecthigh risk population
dc.subjecthuman
dc.subjectM phase cell cycle checkpoint
dc.subjectmismatch repair
dc.subjectneoplasm
dc.subjectnonhuman
dc.subjectpriority journal
dc.subjectprotein function
dc.subjectrecombination repair
dc.subjectshift worker
dc.subjectsignal transduction
dc.subjectsuprachiasmatic nucleus
dc.subjectultraviolet radiation
dc.subjectanimal
dc.subjectchronopharmacology
dc.subjectdrug effects
dc.subjectgenetics
dc.subjectmetabolism
dc.subjectNeoplasms
dc.subjectrisk factor
dc.subjectMammalia
dc.subjectMus
dc.subjectAnimals
dc.subjectAntineoplastic Agents
dc.subjectApoptosis
dc.subjectCircadian Clocks
dc.subjectDNA Damage
dc.subjectDNA Repair
dc.subjectDNA Repair Enzymes
dc.subjectDrug Chronotherapy
dc.subjectHumans
dc.subjectRisk Factors
dc.titleCircadian clock, cancer, and chemotherapy
dc.typeArticle

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