Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/96911
DC FieldValueLanguage
dc.contributor.authorPádua, Diana-
dc.contributor.authorPinto, Débora Filipa-
dc.contributor.authorFigueira, Paula-
dc.contributor.authorPereira, Carlos Filipe-
dc.contributor.authorAlmeida, Raquel-
dc.contributor.authorMesquita, Patrícia-
dc.date.accessioned2022-01-06T16:51:44Z-
dc.date.available2022-01-06T16:51:44Z-
dc.date.issued2021-
dc.identifier.issn1718-7729pt
dc.identifier.urihttps://hdl.handle.net/10316/96911-
dc.description.abstractGastric cancer is a serious health problem worldwide. Although its incidence is decreasing, the five-year survival rate remains low. Thus, it is essential to identify new biomarkers that could promote better diagnosis and treatment of patients with gastric cancer. High-mobility group AT-hook 1 (HMGA1) is a non-histone, chromatin-binding protein that has been found overexpressed in several tumor types. It has been correlated with invasion, metastasis, and drug resistance, leading to worse patient survival. The aim of this work was to evaluate the clinical value of HMGA1 in gastric cancer. HMGA1 expression was analyzed by immunohistochemistry in a single hospital series (n = 323) of gastric adenocarcinoma cases (stages I to IV) with clinicopathological and treatment data. In this series, HMGA1 expression showed no significant relevance as a prognostic biomarker. Nevertheless, a significantly better overall survival was observed in cases with high levels of HMGA1 when they were treated with chemotherapy, compared to the nontreated ones, implying that they can benefit more from treatment than patients with low expression of HMGA1. We thereby show for the first time that HMGA1 expression has a substantial value as a biomarker of response to chemotherapy in gastric cancer. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationPOCI-01-0145-FEDER-007274/Institute for Research and Innovation in Health Sciencespt
dc.relationPOCI-01-0145-FEDER-029017/Cancer Research on Therapy Resistance: From Basic Mechanisms to Novel Targetspt
dc.relationSFRH/BD/146186/2019pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectChemotherapypt
dc.subjectGastric cancerpt
dc.subjectHMGA1pt
dc.subjectPredictive valuept
dc.subjectPrognosispt
dc.titleHMGA1 Has Predictive Value in Response to Chemotherapy in Gastric Cancerpt
dc.typearticle-
degois.publication.firstPage56pt
degois.publication.lastPage67pt
degois.publication.issue1pt
degois.publication.titleCurrent Oncologypt
dc.peerreviewedyespt
dc.identifier.doi10.3390/curroncol29010005pt
degois.publication.volume29pt
dc.date.embargo2021-01-01*
uc.date.periodoEmbargo0pt
item.languageiso639-1en-
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.cerifentitytypePublications-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0002-9724-1382-
Appears in Collections:I&D CNC - Artigos em Revistas Internacionais
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