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Association of insulin-like growth factor II mrna-binding protein 3 (IMP3) expression with prognostic and morphological factors in endometrial cancer

dc.contributor.authorSalum, Silas Otero Reis [UNESP]
dc.contributor.authorCandido, Eduardo Batista
dc.contributor.authorDomingues, Maria Aparecida Custódio [UNESP]
dc.contributor.authorOjopi, Elida Paula Benquique
dc.contributor.authorTonon, Ângela Favorito Santarem [UNESP]
dc.contributor.authorda Silva-Filho, Agnaldo Lopes [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade Federal de Minas Gerais (UFMG)
dc.contributor.institutionFaculdade de Medicina
dc.date.accessioned2025-04-29T18:59:22Z
dc.date.issued2024-01-01
dc.description.abstractObjective: Endometrial cancer (EC) is a heterogeneous disease with recurrence rates ranging from 15 to 20%. The discrimination of cases with a worse prognosis aims, in part, to reduce the length of surgical staging in cases with a better prognosis. This study aimed to evaluate the association between Insulin-like growth factor II mRNA-binding protein 3 (IMP3) expression and prognostic and morphological factors in EC. Methods: This retrospective, cross-sectional, analytical study included 79 EC patients-70 endometrioid carcinoma (EEC) and 9 serous carcinoma (SC)-and 74 benign endometrium controls. IMP3 expression was evaluated by immunohistochemistry-based TMA (Tissue Microarray), and the results were associated with morphological and prognostic factors, including claudins 3 and 4, estrogen and progesterone receptors, TP53, and KI67. Results: IMP3 expression was significantly higher in SC compared to EEC in both extent (p<0.001) and intensity (p=0.044). It was also significantly associated with worse prognostic factors, including degree of differentiation (p=0.024, p<0.001), staging (p<0.001; p<0.001) and metastasis (p=0.002; p<0.001). IMP3 expression was also significant in extent (p=0.002) in endometrial tumors compared with controls. In addition, protein TP53 and KI67 showed significant associations in extent and intensity, respectively. Conclusion: IMP3 expression was associated with worse prognostic factors studied. These findings suggest that IMP3 may be a potential biomarker for EC poorer prognosis.en
dc.description.affiliationUniversidade Estadual Paulista Faculdade de Medicina, SP
dc.description.affiliationUniversidade Federal de Minas Gerais, MG
dc.description.affiliationHospital das Clínicas Faculdade de Medicina, SP
dc.description.affiliationUnespUniversidade Estadual Paulista Faculdade de Medicina, SP
dc.description.sponsorshipUniversidade Estadual Paulista
dc.identifierhttp://dx.doi.org/10.61622/rbgo/2024rbgo61
dc.identifier.citationRevista Brasileira de Ginecologia e Obstetricia, v. 46.
dc.identifier.doi10.61622/rbgo/2024rbgo61
dc.identifier.issn0100-7203
dc.identifier.scopus2-s2.0-85202001948
dc.identifier.urihttps://hdl.handle.net/11449/301788
dc.language.isoeng
dc.relation.ispartofRevista Brasileira de Ginecologia e Obstetricia
dc.sourceScopus
dc.subjectEndometrial neoplasms
dc.subjectImmunohistochemistry
dc.subjectIMP3
dc.subjectInsulin-like growth factor II
dc.subjectPrognosis
dc.titleAssociation of insulin-like growth factor II mrna-binding protein 3 (IMP3) expression with prognostic and morphological factors in endometrial canceren
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationa3cdb24b-db92-40d9-b3af-2eacecf9f2ba
relation.isOrgUnitOfPublication.latestForDiscoverya3cdb24b-db92-40d9-b3af-2eacecf9f2ba
unesp.author.orcid0000-0002-6441-5737[1]
unesp.author.orcid0000-0001-6496-6654[2]
unesp.author.orcid0000-0002-4023-3410[3]
unesp.author.orcid0000-0001-5824-5199[4]
unesp.author.orcid0000-0002-6890-8774[5]
unesp.author.orcid0000-0002-8486-7861[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt

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