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State of art of micronuclei assay in exfoliative cytology as a clinical biomarker of genetic damage in oral carcinogenesis: a systematic review and meta-analysis

dc.contributor.authorAlberto Caponio, Vito Carlo
dc.contributor.authorFrança-Vieira e Silva, Fabio
dc.contributor.authorPopolo, Francesco
dc.contributor.authorGiugliano, Sara
dc.contributor.authorSpizzirri, Francesca
dc.contributor.authorLorenzo-Pouso, Alejandro I.
dc.contributor.authorPadín-Iruegas, María Elena
dc.contributor.authorZhurakivska, Khrystyna
dc.contributor.authorLo Muzio, Lorenzo
dc.contributor.authorLópez-Pintor Muñoz, Rosa María
dc.date.accessioned2024-09-05T09:31:12Z
dc.date.available2024-09-05T09:31:12Z
dc.date.issued2024-07-02
dc.description.abstractOral squamous cell carcinoma (OSCC) is the most common oral malignancy, often preceded by oral potentially malignant disorders (OPMDs). Currently, no clinical biomarker exists to predict malignancy, necessitating OPMD follow-up. Habits and environmental factors, such as smoking, and alcohol consumption, influence OSCC onset. Increased micronuclei (MNs) formation has been observed in the development of OSCC. Non-invasive diagnostic tests like exfoliative cytology offer painless and regular monitoring options. This study evaluates the impact of tobacco, alcohol, and pesticide exposure on MNs occurrence in exfoliative cytology-collected oral mucosal cells, assessing their potential as non-invasive biomarker for OSCC development prediction and monitoring in high-risk patients. Despite results from this meta-analysis supporting the existence of a stepwise increase from controls to patients with OPMD to OSCC, the translation of these findings into clinical practice is limited due to intra- and inter-individual heterogeneity, as well as methodological variability in MNs quantification. Various factors contribute to this heterogeneity, including demographic variables, methodological variability of different laboratories, staining techniques, sample collection location, and patient characteristics. All these points were discussed to provide further insights and improve standardization for future studies.en
dc.description.departmentDepto. de Especialidades Clínicas Odontológicas
dc.description.facultyFac. de Odontología
dc.description.refereedTRUE
dc.description.statuspub
dc.identifier.citationCaponio VCA, Silva FFE, Popolo F, Giugliano S, Spizzirri F, Lorenzo-Pouso AI, Padín-Iruegas ME, Zhurakivska K, Muzio LL, López-Pintor RM. State of art of micronuclei assay in exfoliative cytology as a clinical biomarker of genetic damage in oral carcinogenesis: A systematic review and meta-analysis. Mutat Res Rev Mutat Res. 2024 Jul 2;794:108508. doi: 10.1016/j.mrrev.2024.108508
dc.identifier.doi10.1016/j.mrrev.2024.108508
dc.identifier.essn1388-2139
dc.identifier.issn1383-5742
dc.identifier.officialurlhttps//doi.org/10.1016/j.mrrev.2024.108508
dc.identifier.pmid38964629
dc.identifier.relatedurlhttps://www.sciencedirect.com/science/article/pii/S1383574224000218?via%3Dihub
dc.identifier.urihttps://hdl.handle.net/20.500.14352/107941
dc.journal.titleMutation Research-Reviews in Mutation Research
dc.language.isoeng
dc.page.initial108508
dc.publisherElsevier
dc.rightsAttribution-NonCommercial 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subject.cdu616.31 Boca-enfermedades
dc.subject.cdu615.277.4 Carcinógenos
dc.subject.cdu616-076.5 Citodiagnóstico
dc.subject.keywordMeta-analysis
dc.subject.keywordMicronucleus tests
dc.subject.keywordMouth neoplasms
dc.subject.keywordPesticides
dc.subject.keywordRisk factors
dc.subject.keywordTobacco products
dc.subject.ucmOdontología (Odontología)
dc.subject.ucmMicrobiología médica
dc.subject.unesco3213.13 Ortodoncia-Estomatología
dc.subject.unesco3207.03 Carcinogénesis
dc.titleState of art of micronuclei assay in exfoliative cytology as a clinical biomarker of genetic damage in oral carcinogenesis: a systematic review and meta-analysisen
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number794
dspace.entity.typePublication
relation.isAuthorOfPublicationb686e7da-b3c7-41a9-bbe0-8c1f30cbc553
relation.isAuthorOfPublication.latestForDiscoveryb686e7da-b3c7-41a9-bbe0-8c1f30cbc553

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