Proposing Specific Neuronal Epithelial-to-Mesenchymal Transition Genes as an Ancillary Tool for Differential Diagnosis among Pulmonary Neuroendocrine Neoplasms

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Autor(es): dc.contributorUniversidade de São Paulo (USP)-
Autor(es): dc.contributorUniversidade Estadual Paulista (UNESP)-
Autor(es): dc.contributorAC Camargo Cancer Center-
Autor(es): dc.contributorBarretos Cancer Hospital-
Autor(es): dc.contributorFundação Oncocentro do Estado de São Paulo (FOSP)-
Autor(es): dc.creatorPrieto, Tabatha Gutierrez-
Autor(es): dc.creatorBaldavira, Camila Machado-
Autor(es): dc.creatorMachado-Rugolo, Juliana-
Autor(es): dc.creatorOlivieri, Eloisa Helena Ribeiro-
Autor(es): dc.creatorda Silva, Eduardo Caetano Abilio-
Autor(es): dc.creatorAb’ Saber, Alexandre Muxfeldt-
Autor(es): dc.creatorTakagaki, Teresa Yae-
Autor(es): dc.creatorCapelozzi, Vera Luiza-
Data de aceite: dc.date.accessioned2025-08-21T22:49:33Z-
Data de disponibilização: dc.date.available2025-08-21T22:49:33Z-
Data de envio: dc.date.issued2023-07-29-
Data de envio: dc.date.issued2023-07-29-
Data de envio: dc.date.issued2022-11-30-
Fonte completa do material: dc.identifierhttp://dx.doi.org/10.3390/genes13122309-
Fonte completa do material: dc.identifierhttp://hdl.handle.net/11449/249019-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/11449/249019-
Descrição: dc.descriptionPulmonary neuroendocrine neoplasms (PNENs) are currently classified into four major histotypes, including typical carcinoid (TC), atypical carcinoid (AC), large cell neuroendocrine carcinoma (LCNEC), and small cell lung carcinoma (SCLC). This classification was designed to be applied to surgical specimens mostly anchored in morphological parameters, resulting in considerable overlapping among PNENs, which may result in important challenges for clinicians’ decisions in the case of small biopsies. Since PNENs originate from the neuroectodermic cells, epithelial-to-mesenchymal transition (EMT) gene expression shows promise as biomarkers involved in the genotypic transformation of neuroectodermic cells, including mutation burden with the involvement of chromatin remodeling genes, apoptosis, and mitosis rate, leading to modification in final cellular phenotype. In this situation, additional markers also applicable to biopsy specimens, which correlate PNENs subtypes with systemic treatment response, are much needed, and current potential candidates are neurogenic EMT genes. This study investigated EMT genes expression and its association with PNENs histotypes in tumor tissues from 24 patients with PNENs. PCR Array System for 84 EMT-related genes selected 15 differentially expressed genes among the PNENs, allowing to discriminate TC from AC, LCNEC from AC, and SCLC from AC. Functional enrichment analysis of the EMT genes differentially expressed among PNENs subtypes showed that they are involved in cellular proliferation, extracellular matrix degradation, regulation of cell apoptosis, oncogenesis, and tumor cell invasion. Interestingly, four EMT genes (MAP1B, SNAI2, MMP2, WNT5A) are also involved in neurological diseases, in brain metastasis, and interact with platinum-based chemotherapy and tyrosine–kinase inhibitors. Collectively, these findings emerge as an important ancillary tool to improve the strategies of histologic diagnosis in PNENs and unveil the four EMT genes that can play an important role in driving chemical response in PNENs.-
Descrição: dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
Descrição: dc.descriptionLaboratory of Genomics and Histomorphometry Department of Pathology University of São Paulo Medical School (USP), SP-
Descrição: dc.descriptionHealth Technology Assessment Center (NATS) Clinical Hospital (HCFMB) Medical School of São Paulo State University (UNESP), SP-
Descrição: dc.descriptionInternational Center of Research/CIPE AC Camargo Cancer Center, SP-
Descrição: dc.descriptionMolecular Oncology Research Center Barretos Cancer Hospital, SP-
Descrição: dc.descriptionFundação Oncocentro do Estado de São Paulo (FOSP), SP-
Descrição: dc.descriptionDivision of Pneumology Instituto do Coração (Incor) Medical School of University of São Paulo, SP-
Descrição: dc.descriptionHealth Technology Assessment Center (NATS) Clinical Hospital (HCFMB) Medical School of São Paulo State University (UNESP), SP-
Descrição: dc.descriptionCNPq: 303735/2021-0-
Idioma: dc.languageen-
Relação: dc.relationGenes-
???dc.source???: dc.sourceScopus-
Palavras-chave: dc.subjectdiagnosis-
Palavras-chave: dc.subjectepithelial-to-mesenchymal transition-
Palavras-chave: dc.subjectmetastasis-
Palavras-chave: dc.subjectmorphology-
Palavras-chave: dc.subjectpulmonary neuroendocrine neoplasms-
Título: dc.titleProposing Specific Neuronal Epithelial-to-Mesenchymal Transition Genes as an Ancillary Tool for Differential Diagnosis among Pulmonary Neuroendocrine Neoplasms-
Tipo de arquivo: dc.typelivro digital-
Aparece nas coleções:Repositório Institucional - Unesp

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