Pulmonary Neuroendocrine Neoplasms Overexpressing Epithelial-Mesenchymal Transition Mechanical Barriers Genes Lack Immune-Suppressive Response and Present an Increased Risk of Metastasis

Autor(es):Mostrar menos -

Prieto, Tabatha Gutierrez ^[1] ; Baldavira, Camila Machado ^[1] ; Machado-Rugolo, Juliana ^{[1, 2]} ; Farhat, Cecilia ^[1] ; Ribeiro Olivieri, Eloisa Helena ^[3] ; de Sa, Vanessa Karen ^[3] ; Abilio da Silva, Eduardo Caetano ^[4] ; Balancin, Marcelo Luiz ^[1] ; Ab Saber, Alexandre Muxfeldt ^[1] ; Takagaki, Teresa Yae ^[5] ; Cordeiro de Lima, Vladmir Claudio ^{[6, 7]} ; Capelozzi, Vera Luiza ^[1]

Afiliação do(s) autor(es)

^[1] Univ Sao Paulo, Dept Pathol, Med Sch USP, Sao Paulo - Brazil

^[2] Sao Paulo State Univ UNESP, Clin Hosp HCFMB, Hlth Technol Assessment Ctr NATS, Med Sch, Botucatu, SP - Brazil

^[3] AC Camargo Canc Ctr, Int Ctr Res CIPE, Sao Paulo - Brazil

^[4] Barretos Canc Hosp, Mol Oncol Res Ctr, Sao Paulo - Brazil

^[5] Univ Sao Paulo, Inst Coracao Incor, Div Pneumol, Med Sch, Sao Paulo - Brazil

^[6] Rede DOr Sao Paulo, Oncol, Sao Paulo - Brazil

^[7] Inst Canc Estado Sao Paulo ICESP, Dept Clin Oncol, Sao Paulo - Brazil

• Tipo de documento: Artigo Científico
• Fonte: FRONTIERS IN ONCOLOGY; v. 11, AUG 30 2021.
• Citações Web of Science: 0

Resumo

Typical carcinoids (TC), atypical carcinoids (AC), large cell neuroendocrine carcinomas (LCNEC), and small cell lung carcinomas (SCLC) encompass a bimodal spectrum of metastatic tumors with morphological, histological and histogenesis differences, The hierarchical structure reveals high cohesiveness between neoplastic cells by mechanical desmosomes barrier assembly in carcinoid tumors and LCNEC, while SCLC does not present an organoid arrangement in morphology, the neoplastic cells are less cohesive. However, the molecular mechanisms that lead to PNENs metastasis remain largely unknown and require further study. In this work, epithelial to mesenchymal transition (EMT) transcription factors were evaluated using a set of twenty-four patients with surgically resected PNENs, including carcinomas. Twelve EMT transcription factors (BMP1, BMP7, CALD1, CDH1, COL3A1, COL5A2, EGFR, ERBB3, PLEK2, SNAI2, STEAP1, and TCF4) proved to be highly expressed among carcinomas and downregulated in carcinoid tumors, whereas upregulation of BMP1, CDH2, KRT14 and downregulation of CAV2, DSC2, IL1RN occurred in both histological subtypes. These EMT transcription factors identified were involved in proliferative signals, epithelium desmosomes assembly, and cell motility sequential steps that support PNENs invasion and metastasis in localized surgically resected primary tumor. We used a two-stage design where we first examined the candidate EMT transcription factors using a whole-genome screen, and subsequently, confirmed EMT-like changes by transmission electron microscopy and then, the EMT-related genes that were differentially expressed among PNENs subtypes were predicted through a Metascape analysis by in silico approach. A high expression of these EMT transcription factors was significantly associated with lymph node and distant metastasis. The sequential steps for invasion and metastasis were completed by an inverse association between functional barrier created by PD-L1 immunosuppressive molecule and EMT transcriptional factors. Our study implicates upregulation of EMT transcription factors to high proliferation rates, mechanical molecular barriers disassembly and increased cancer cell motility, as a critical molecular event leading to metastasis risk in PNENs thus emerging as a promising tool to select and customize therapy.</p> (AU)

• Processo FAPESP: 18/20403-6 - Marcadores biomoleculares de proliferação e remodelamento em doenças respiratórias agudas e crônicas: promissores alvos terapêuticos
• Beneficiário: Vera Luiza Capelozzi
• Modalidade de apoio: Auxílio à Pesquisa - Temático
• Processo FAPESP: 19/12151-0 - Avaliação da expressão proteica de DLL-3 e ASCL-1 como nova perspectiva em biomarcadores para o diagnóstico precoce dos carcinomas pulmonares de pequenas células
• Beneficiário: Tabatha Gutierrez Prieto Martins Rocha
• Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado