Publication:
The impact of circadian rhythm disruption on oxaliplatin tolerability and pharmacokinetics in Cry1<SUP>-/-</SUP>Cry2<SUP>-/-</SUP> mice under constant darkness

dc.contributor.coauthorAkyel, Yasemin Kubra
dc.contributor.coauthorOzturk Seyhan, Narin
dc.contributor.coauthorGül, Şeref
dc.contributor.coauthorSelby, Christopher P.
dc.contributor.coauthorOkyar, Alper
dc.contributor.departmentDepartment of Molecular Biology and Genetics
dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.departmentDepartment of Chemical and Biological Engineering
dc.contributor.kuauthorÇelik, Melis
dc.contributor.kuauthorTaşkın, Ali Cihan
dc.contributor.kuauthorKavaklı, İbrahim Halil
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.contributor.schoolcollegeinstituteResearch Center
dc.contributor.schoolcollegeinstituteCollege of Engineering
dc.date.accessioned2025-05-22T10:34:59Z
dc.date.available2025-05-22
dc.date.issued2025
dc.description.abstractCircadian rhythms, the 24-h oscillations of biological activities guided by the molecular clock, play a pivotal role in regulating various physiological processes in organisms. The intricate relationship between the loss of circadian rhythm and its influence on the tolerability and pharmacokinetic properties of anticancer drugs is poorly understood. In our study, we investigated the effects of oxaliplatin, a commonly used anticancer drug, on Cry1-/- and Cry2-/- mice (Cry DKO mice) under darkness conditions, where they exhibit free-running phenotype. We administered oxaliplatin at a dosage of 12 mg/kg/day at two distinct circadian times, CT8 and CT16, under constant darkness conditions to Cry DKO mice and their wild type littermates. Our results revealed a striking disparity in oxaliplatin tolerance between Cry DKO mice and their wild-type counterparts. Oxaliplatin exhibited severe toxicity in Cry DKO mice at both CT8 and CT16, in contrast to the wild type mice. Pharmacokinetic analyses suggested that such toxicity was a result of high concentrations of oxaliplatin in the serum and liver of Cry DKO mice after repeated dose injections. To understand the molecular basis of such intolerance, we performed RNA-seq studies using mouse livers. Our findings from the RNA-seq analysis highlighted the substantial impact of circadian rhythm disruption on gene expression, particularly affecting genes involved in detoxification and xenobiotic metabolism, such as the Gstm gene family. This dysregulation in detoxification pathways in Cry DKO mice likely contributes to the increased toxicity of oxaliplatin. In conclusion, our study highlights the crucial role of an intact molecular clock in dictating the tolerability of oxaliplatin. These findings emphasize the necessity of considering circadian rhythms in the administration of anticancer drugs, providing valuable insights into optimizing treatment strategies for cancer patients.
dc.description.fulltextYes
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessGold OA
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuTÜBİTAK
dc.description.sponsorshipResearch Fund of Istanbul University (Project no. TSG-2017-24537)
dc.description.sponsorshipTÜBİTAK
dc.description.versionPublished Version
dc.identifier.doi10.1007/s00204-025-03968-7
dc.identifier.eissn1432-0738
dc.identifier.embargoNo
dc.identifier.endpage1429
dc.identifier.filenameinventorynoIR06274
dc.identifier.issn0340-5761
dc.identifier.issue4
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85218817943
dc.identifier.startpage1417
dc.identifier.urihttps://doi.org/10.1007/s00204-025-03968-7
dc.identifier.urihttps://hdl.handle.net/20.500.14288/29414
dc.identifier.volume99
dc.identifier.wos001412702200001
dc.keywordsOxaliplatin
dc.keywordsChronopharmacokinetics
dc.keywordsChronotoxicity
dc.keywordsCryptochrome double-knockout mice
dc.keywordsCircadian clock
dc.language.isoeng
dc.publisherSpringer Nature
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofArchives of Toxicology
dc.relation.openaccessYes
dc.rightsCC BY (Attribution)
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectToxicology
dc.titleThe impact of circadian rhythm disruption on oxaliplatin tolerability and pharmacokinetics in Cry1<SUP>-/-</SUP>Cry2<SUP>-/-</SUP> mice under constant darkness
dc.typeJournal Article
dspace.entity.typePublication
person.familyNameÇelik
person.familyNameTaşkın
person.familyNameKavaklı
person.givenNameMelis
person.givenNameAli Cihan
person.givenNameİbrahim Halil
relation.isOrgUnitOfPublicationaee2d329-aabe-4b58-ba67-09dbf8575547
relation.isOrgUnitOfPublication91bbe15d-017f-446b-b102-ce755523d939
relation.isOrgUnitOfPublicationc747a256-6e0c-4969-b1bf-3b9f2f674289
relation.isOrgUnitOfPublication.latestForDiscoveryaee2d329-aabe-4b58-ba67-09dbf8575547
relation.isParentOrgUnitOfPublicationaf0395b0-7219-4165-a909-7016fa30932d
relation.isParentOrgUnitOfPublicationd437580f-9309-4ecb-864a-4af58309d287
relation.isParentOrgUnitOfPublication8e756b23-2d4a-4ce8-b1b3-62c794a8c164
relation.isParentOrgUnitOfPublication.latestForDiscoveryaf0395b0-7219-4165-a909-7016fa30932d

Files