Predictive value of CDKN2A/p16INK4a expression in the malignant transformation of oral potentially malignant disorders: Systematic review and meta-analysis

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Cirurxía e Especialidades Médico-Cirúrxicases_ES
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Medicinaes_ES
dc.contributor.authorLorenzo Pouso, Alejandro Ismael
dc.contributor.authorCaponio, Vito Carlo Alberto
dc.contributor.authorVieira e Silva, Fábio França
dc.contributor.authorPérez-Jardón, Alba
dc.contributor.authorÁlvarez-Calderón-Iglesias, Óscar
dc.contributor.authorGándara Vila, Pilar
dc.contributor.authorPannone, Giuseppe
dc.contributor.authorPérez-Sayáns García, Mario
dc.date.accessioned2023-11-13T11:12:03Z
dc.date.available2023-11-13T11:12:03Z
dc.date.issued2023-06-29
dc.description.abstractBackground Management of oral potentially malignant disorders (OPMDs) is still challenging. Despite the diagnostic ascertainment by bioptic examination, this method is poorly informative of the prognosis and subsequent malignant transformation. Prognosis is based on histological findings by grading of dysplasia. Immunohistochemical expression of p16INK4a has been investigated in different studies, with controversial results. In this scenario, we systematically revised the current evidence about p16INK4a immunohistochemical expression and the risk of malignization of OPMDs. Material and methods After a proper set of keywords combination, 5 databases were accessed and screened to select eligible studies. The protocol was previously registered on PROSPERO (Protocol ID: CRD42022355931). Data were obtained directly from the primary studies as a measure to determine the relationship between CDKN2A/P16INK4a expression and the malignant transformation of OPMDs. Heterogeneity and publication bias were investigated by different tools, such as Cochran's Q test, Galbraith plot and Egger and Begg Mazumdar’s rank tests. Results Meta-analysis revealed a twofold increased risk to malignant development (RR = 2.01, 95% CI = 1.36–2.96 - I2 = 0%). Subgroup analysis did not highlight any relevant heterogeneity. Galbraith plot showed that no individual study could be considered as an important outlier. Conclusion Pooled analysis showed that p16INK4a assessment may arise adjunct tool to dysplasia grading, leading to an optimized determination of the potential progression to cancer of OPMDs. The p16INK4a overexpression analysis by immunohistochemistry techniques has a multitude of virtues that may facilitate its incorporation in the day-to-day prognostic study of OPMDses_ES
dc.description.peerreviewedSIes_ES
dc.identifier.citationPathology - Research and Practice 248 (2023) 154656es_ES
dc.identifier.doi10.1016/j.prp.2023.154656
dc.identifier.issn0344-0338
dc.identifier.urihttp://hdl.handle.net/10347/31265
dc.journal.titlePathology - Research and Practice
dc.language.isoenges_ES
dc.page.initial154656
dc.publisherElsevieres_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.prp.2023.154656es_ES
dc.rights© 2023 The Authors. Published by Elsevier GmbH. This article is available under the Creative Commons CC-BY-NC-ND license and permits non-commercial use of the work as published, without adaptation or alteration provided the work is fully attributedes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectp16INK4a Genees_ES
dc.subjectOPMDes_ES
dc.subjectMeta-analysises_ES
dc.subjectPrognosises_ES
dc.subjectImmunohistochemistryes_ES
dc.titlePredictive value of CDKN2A/p16INK4a expression in the malignant transformation of oral potentially malignant disorders: Systematic review and meta-analysises_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dc.volume.number248
dspace.entity.typePublication
relation.isAuthorOfPublicationfba09624-8717-4db3-afdd-e018d34469f3
relation.isAuthorOfPublication1fc179e1-51df-42a8-8961-420b8d496a9e
relation.isAuthorOfPublication.latestForDiscoveryfba09624-8717-4db3-afdd-e018d34469f3

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