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dc.contributor.authorBermúdez, Ana
dc.contributor.authorArranz-Salas, Isabel María 
dc.contributor.authorMercado-Sáenz, Silvia 
dc.contributor.authorLópez-Villodres, Juan Antonio 
dc.contributor.authorGonzález, Virginia
dc.contributor.authorRíus-Díaz, Francisca 
dc.contributor.authorOrtega-Jiménez, María Victoria 
dc.contributor.authorAlba-Linero, Carmen 
dc.contributor.authorHierro-Martín, María Isabel 
dc.contributor.authorBermúdez-Flores, Diego Teófilo 
dc.date.accessioned2024-10-02T10:02:31Z
dc.date.available2024-10-02T10:02:31Z
dc.date.created2024-09-25
dc.date.issued2021-03-21
dc.identifier.citationBermúdez A, Arranz-Salas I, Mercado S, López-Villodres JA, González V, Ríus F, Ortega MV, Alba C, Hierro I, Bermúdez D. Her2-Positive and Microsatellite Instability Status in Gastric Cancer-Clinicopathological Implications. Diagnostics (Basel). 2021 May 25;11(6):944. doi: 10.3390/diagnostics11060944. PMID: 34070574; PMCID: PMC8228707.es_ES
dc.identifier.urihttps://hdl.handle.net/10630/34194
dc.descriptionInstitutional Review Board Statement: The study was conducted according to the Declaration of Helsinki, national and international guidelines and approved by the Provincial Research Ethics Committee of Malaga, Spain (approval 21 February 2019, number TFG-NCCG-2019). Informed Consent Statement: All the subjects provided written informed consent before participating in the study. Written informed consent for publication obtained from participating patients who can be identified. Data Availability Statement: The data that support the findings of this study are available from the corresponding author upon reasonable request. Acknowledgments: The authors would like to thank Maria Repice for her help with the English version of the text.es_ES
dc.description.abstractGastric cancer (GC) is one of the leading causes of cancer-related death. The combination of new molecular classifications with clinicopathological data could contribute to the individualization of patients and to the development of new therapeutic strategies. We examined the various associations in two molecular types of GC: HER2-positive (human epidermal growth factor receptor 2) and microsatellite instability (MSI), assessing their influence on treatment and prognosis. A retrospective study of 142 GC patients was performed with molecular characterization through HER2 overexpression and DNA repair protein expression for MSI. The percentage of HER2-positive tumors was 13.4%, predominantly in men. Correlations were found with intestinal type, metastases, advanced stages and chemotherapy. Almost 75% of HER2-positive patients died. MSI occurred in 16.2%, associated with advanced age, female sex, distal location and intestinal type. These patients had few metastases and low stages. The percentage of deaths was higher among MSI patients who received perioperative chemotherapy. The determination of HER2 and MSI status in GC is important for their association with specific clinicopathological features and for their prognostic and predictive value.es_ES
dc.description.sponsorshipThis research was financially supported by the Department of Human Physiology, Human Histology, Anatomical Pathology and Physical Education (Histology Unit), University of Malaga and by the Department of Anatomical Pathology, Virgen de la Victoria University Hospital.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectEstómago - Cánceres_ES
dc.subject.othergastric canceres_ES
dc.subject.othermolecular classificationes_ES
dc.subject.otherHER2es_ES
dc.subject.othermicrosatellite instabilityes_ES
dc.subject.otherclinicopathological featureses_ES
dc.titleHer2-Positive and Microsatellite Instability Status in Gastric Cancer—Clinicopathological Implicationses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.centroFacultad de Medicinaes_ES
dc.identifier.doi10.3390/diagnostics11060944
dc.rights.ccAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES


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