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Low EGFL7 expression is associated with high lymph node spread and invasion of lymphatic vessels in colorectal cancer

dc.contributor.authorde Oliveira, Cristiane [UNESP]
dc.contributor.authorMartins, Sandra Fátima Fernandes
dc.contributor.authorGonçalves, Paola Gyuliane [UNESP]
dc.contributor.authorLimone, Gabriel Augusto
dc.contributor.authorLongatto-Filho, Adhemar
dc.contributor.authorReis, Rui Manuel
dc.contributor.authorBidinotto, Lucas Tadeu [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionBarretos Cancer Hospital
dc.contributor.institutionUniversity of Minho
dc.contributor.institutionICVS/3B’s – PT Government Associate Laboratory
dc.contributor.institutionBraga Hospital
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionDr. Paulo Prata – FACISB
dc.date.accessioned2025-04-29T18:50:20Z
dc.date.issued2023-12-01
dc.description.abstractStudies indicate EGFL7 as an important gene in controlling angiogenesis and cancer growth, including in colorectal cancer (CRC). Anti-EGFL7 agents are being explored, yet without promising results. Therefore, the role of EGFL7 in CRC carcinogenesis should be investigated. This study aimed to evaluate the prognostic value of EGFL7 expression in CRC and the signaling pathways influenced by this gene. EGFL7 expression was evaluated through immunohistochemistry in 463 patients diagnosed with CRC and further associated with clinicopathological data, angiogenesis markers and survival. In silico analyzes were performed with colon adenocarcinoma data from The Cancer Genome Atlas. Analysis of enriched gene ontology and pathways were performed using the differentially expressed genes. 77.7% of patients presented low EGFL7 expression, which was associated with higher lymph node spread and invasion of lymphatic vessels, with no impact on survival. Additionally, low EGFL7 expression was associated with high VEGFR2 expression. Finally, we found in silico that EGFL7 expression was associated with cell growth, angiogenesis, and important pathways such as VEGF, Rap-1, MAPK and PI3K/Akt. Expression of EGFL7 in tumor cells may be associated with important pathways that can alter functions related to tumor invasive processes, preventing recurrence and metastatic process.en
dc.description.affiliationBotucatu Medical School Department of Pathology UNESP – Univ. Estadual Paulista
dc.description.affiliationMolecular Oncology Research Center Barretos Cancer Hospital
dc.description.affiliationLife and Health Sciences Research Institute (ICVS) School of Medicine University of Minho
dc.description.affiliationICVS/3B’s – PT Government Associate Laboratory
dc.description.affiliationColorectal Unit Braga Hospital
dc.description.affiliationDepartment of Pathology Barretos Cancer Hospital
dc.description.affiliationMedical Laboratory of Medical Investigation (LIM) 14 Department of Pathology Medical School University of São Paulo
dc.description.affiliationSchool of Medicine University of Minho
dc.description.affiliationBarretos School of Health Sciences Dr. Paulo Prata – FACISB
dc.description.affiliationUnespBotucatu Medical School Department of Pathology UNESP – Univ. Estadual Paulista
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2021/14253-4
dc.identifierhttp://dx.doi.org/10.1038/s41598-023-47132-6
dc.identifier.citationScientific Reports, v. 13, n. 1, 2023.
dc.identifier.doi10.1038/s41598-023-47132-6
dc.identifier.issn2045-2322
dc.identifier.scopus2-s2.0-85176435430
dc.identifier.urihttps://hdl.handle.net/11449/300690
dc.language.isoeng
dc.relation.ispartofScientific Reports
dc.sourceScopus
dc.titleLow EGFL7 expression is associated with high lymph node spread and invasion of lymphatic vessels in colorectal canceren
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationa3cdb24b-db92-40d9-b3af-2eacecf9f2ba
relation.isOrgUnitOfPublication.latestForDiscoverya3cdb24b-db92-40d9-b3af-2eacecf9f2ba
unesp.author.orcid0000-0002-6909-8347[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt

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