The multifaceted impact of circadian disruption on cancer risk: insights and economic implications

dc.contributor.authorClemente Suárez, Vicente Javier
dc.contributor.authorNavarro Jiménez, Eduardo
dc.contributor.authorBenítez Agudelo, Juan Camilo
dc.contributor.authorBeltrán Velasco, Ana Isabel
dc.contributor.authorBelinchón de Miguel, Pedro
dc.contributor.authorRamos Campo, Domingo Jesús
dc.contributor.authorVillanueva Tobaldo, Carlota Valeria
dc.contributor.authorMartín Rodríguez, Alexandra
dc.contributor.authorTornero Aguilera, José Francisco
dc.date.accessioned2025-06-26T12:11:29Z
dc.date.available2025-06-26T12:11:29Z
dc.date.issued2025
dc.description.abstractBackground Circadian disruption has emerged as a significant risk factor for cancer, driven by mechanisms such as hormonal imbalances, impaired DNA repair, immune suppression, and metabolic dysregulation. Modern societal patterns—shift work, artificial light at night, and irregular sleep schedules—have exacerbated these risks. Methods We conducted a systematic review following PRISMA guidelines, screening over 500 studies published between 2003 and 2023 from PubMed, Scopus, Embase, ScienceDirect, and Web of Science. Inclusion criteria focused on peer-reviewed epidemiological and mechanistic studies linking circadian disruption with cancer risk. The Newcastle-Ottawa Scale was used for methodological quality assessment. Results A total of 75 high-quality studies were included. Strong evidence supports associations between circadian disruption and breast, prostate, and colorectal cancers, with limited but emerging evidence for melanoma and bladder cancer. Mechanistic pathways involve melatonin suppression, dysregulation of CLOCK and BMAL1 genes, reduced natural killer cell activity, and chronic inflammation due to metabolic imbalance. Light-at-night (LAN) exposure and prolonged night shift work were consistently identified as major risk factors. Furthermore, economic analyses reveal a substantial burden due to increased healthcare costs and productivity losses, particularly in shift work-dominated sectors. Conclusions Circadian misalignment is a critical, yet often overlooked, contributor to cancer incidence and associated economic burdens. Public health strategies—such as regulating shift schedules, reducing LAN exposure, and promoting chronotherapy—are essential to mitigate these risks. Further research should address sex-based differences, improve exposure measurement, and extend investigations to low- and middle-income countries.spa
dc.description.filiationUEMspa
dc.description.impact9.4 Q1 JCR 2024spa
dc.description.impact2.441 Q1 SJR 2024spa
dc.description.impactNo data IDR 2023spa
dc.description.sponsorshipSin financiaciónspa
dc.identifier.citationClemente-Suarez, V. J., Navarro-Jiménez, E., Benitez-Agudelo, J. C., Beltrán-Velasco, A. I., Belinchón-deMiguel, P., Ramos-Campo, D. J., Villanueva-Tobaldo, C. V., Martín-Rodríguez, A., & Tornero-Aguilera, J. F. (2025). The multifaceted impact of circadian disruption on cancer risk: Insights and economic implications. Journal of the National Cancer Center, S2667005425000651. https://doi.org/10.1016/j.jncc.2025.04.005spa
dc.identifier.doi10.1016/j.jncc.2025.04.005
dc.identifier.issn2096-8663
dc.identifier.urihttp://hdl.handle.net/11268/14698
dc.language.isoengspa
dc.peerreviewedSispa
dc.relation.publisherversionhttps://doi.org/10.1016/j.jncc.2025.04.005spa
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.accessRightsopen accessspa
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.sdgGoal 3: Ensure healthy lives and promote well-being for all at all agesspa
dc.subject.unescoCiencias médicasspa
dc.subject.unescoCoste de la vidaspa
dc.subject.unescoCáncerspa
dc.titleThe multifaceted impact of circadian disruption on cancer risk: insights and economic implicationsspa
dc.typejournal articlespa
dc.type.hasVersionAMspa
dspace.entity.typePublication
relation.isAuthorOfPublicationa2e25626-16b1-41bc-9c67-8de8ce6e007d
relation.isAuthorOfPublicationf4edd5d4-d8a2-44b8-b2ae-92c029972f6a
relation.isAuthorOfPublication20d7ed6e-e9e5-4056-8372-a9631a99ced0
relation.isAuthorOfPublication.latestForDiscoverya2e25626-16b1-41bc-9c67-8de8ce6e007d

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