Use este identificador para citar ou linkar para este item: https://ninho.inca.gov.br/jspui/handle/123456789/11480
Título: Oral Lichen Planus and Oral Squamous Cell Carcinoma share key oncogenic signatures
Autor(es): Lanna, Cristóvão Antunes de
Silva, Beatriz Nascimento Monteiro da
Melo, Andreia Cristina de
Bonamino, Martín Hernan
Alves, Lísia Daltro Borges
Pinto, Luis Felipe Ribeiro
Cardoso, Abel Silveira
Antunes, Héliton Spíndola
Boroni, Mariana
Goldemberg, Daniel Cohen
Instituto Nacional de Câncer.
Universidade Federal do Rio de Janeiro
Universidade de Campinas
University College London
Palavras-chave: Carcinogênese/genética
Carcinogenesis/genetics
Carcinogénesis/genética
Carcinoma de Células Escamosas/genética
Carcinoma, Squamous Cell/genetics
Carcinoma de Células Escamosas/genética
Neoplasias de Cabeça e Pescoço
Head and Neck Neoplasms
Neoplasias de Cabeza y Cuello
Líquen Plano Bucal
Lichen Planus, Oral
Liquen Plano Oral
Data do documento: 30-Nov-2022
Editor: Scientifc Reports v. 12, n. 1. p.20645
Resumo: To investigate similarities in the gene profle of Oral Lichen Planus and Oral Squamous Cell Carcinoma that may justify a carcinogenic potential, we analyzed the gene expression signatures of Oral Lichen Planus and Oral Squamous Cell Carcinoma in early and advanced stages. Based on gene expression data from public databases, we used a bioinformatics approach to compare expression profles, estimate immune infltrate composition, identify diferentially and co-expressed genes, and propose putative therapeutic targets and associated drugs. Our results revealed gene expression patterns related to processes of keratinization, keratinocyte diferentiation, cell proliferation and immune response in common between Oral Lichen Planus and early and advanced Oral Squamous Cell Carcinoma, with the cornifed envelope formation and antigen processing cross-presentation pathways in common between Oral Lichen Planus and early Oral Squamous Cell Carcinoma. Together, these results reveal that key tumor suppressors and oncogenes such as PI3, SPRR1B and KRT17, as well as genes associated with diferent immune processes such as CXCL13, HIF1A and IL1B are dysregulated in OLP.
URI: https://ninho.inca.gov.br/jspui/handle/123456789/11480
Aparece nas coleções:Artigo de Periódicos da Pesquisa Clínica
Artigos de Periódicos da Pesquisa Experimental e Translacional

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