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dc.contributor.authorRamos García, Pablo 
dc.contributor.authorGonzález Moles, Miguel Ángel 
dc.date.accessioned2022-03-21T07:35:13Z
dc.date.available2022-03-21T07:35:13Z
dc.date.issued2022-01-18
dc.identifier.citationRamos-García, P.; González-Moles, M.Á. Prognostic and Clinicopathological Significance of the Aberrant Expression of beta-Catenin in Oral Squamous Cell Carcinoma: A Systematic Review and Meta-Analysis. Cancers 2022, 14, 479. [https://doi.org/10.3390/cancers14030479]es_ES
dc.identifier.urihttp://hdl.handle.net/10481/73577
dc.descriptionWe would like to thank the research group CTS-392 (Plan Andaluz de Investigacion, Junta de Andalucia, Spain).es_ES
dc.description.abstractThis systematic review and meta-analysis aims to evaluate the prognostic and clinicopathological significance of the aberrant expression of beta-catenin (assessed through the immunohistochemical loss of membrane expression, cytoplasmic and nuclear expression) in oral squamous cell carcinoma (OSCC). We searched for primary-level studies published before October-2021 through PubMed, Embase, Web of Science, Scopus, and Google Scholar, with no limitation in regard to their publication date or language. We evaluated the methodological quality and risk of bias of the studies included using the QUIPS tool, carried out meta-analyses, explored heterogeneity and their sources across subgroups and meta-regression, and conducted sensitivity and small-study effects analyses. Forty-one studies (2746 patients) met inclusion criteria. The aberrant immunohistochemical expression of beta-catenin was statistically associated with poor overall survival (HR = 1.77, 95% CI = 1.20-2.60, p = 0.004), disease-free survival (HR = 2.44, 95% CI = 1.10-5.50, p = 0.03), N+ status (OR = 2.39, 95% CI = 1.68-3.40, p < 0.001), higher clinical stage (OR = 2.40, 95% CI = 1.58-3.63, p < 0.001), higher tumour size (OR = 1.76, 95% CI = 1.23-2.53, p = 0.004), and moderately-poorly differentiated OSCC (OR = 1.57, 95% CI = 1.09-2.25, p = 0.02). The loss of beta-catenin in the cell membrane showed the largest effect size in most of meta-analyses (singularly for poor overall survival [HR = 2.37, 95% CI = 1.55-3.62, p < 0.001], N+ status [OR = 3.44, 95% CI = 2.40-4.93, p < 0.001] and higher clinical stage [OR = 2.51, 95% CI = 1.17-5.35, p = 0.02]). In conclusion, our findings indicate that immunohistochemical assessment of the aberrant expression of beta-catenin could be incorporated as an additional and complementary routine prognostic biomarker for the assessment of patients with OSCC.es_ES
dc.description.sponsorshipJunta de Andalucia CTS-392es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAtribución 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectBeta-catenines_ES
dc.subjectCTNNBes_ES
dc.subjectWnt signalling pathwayes_ES
dc.subjectEpithelial-mesenchymal transitiones_ES
dc.subjectOral squamous cell carcinomaes_ES
dc.subjectPrognosis es_ES
dc.subjectBiomarkeres_ES
dc.subjectSystematic reviewes_ES
dc.subjectMeta-analysises_ES
dc.titlePrognostic and Clinicopathological Significance of the Aberrant Expression of beta-Catenin in Oral Squamous Cell Carcinoma: A Systematic Review and Meta-Analysises_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.3390/cancers14030479
dc.type.hasVersionVoRes_ES


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