Busca avançada
Ano de início
Entree


Genome-wide promoter methylation profiling in a cellular model of melanoma progression reveals markers of malignancy and metastasis that predict melanoma survival

Texto completo
Autor(es):
Mostrar menos -
Rius, Flavia E. ; Papaiz, Debora D. ; Azevedo, Hatylas F. Z. ; Ayub, Ana Luisa P. ; Pessoa, Diogo O. ; Oliveira, Tiago F. ; Loureiro, Ana Paula M. ; Andrade, Fernando ; Fujita, Andre ; Reis, Eduardo M. ; Mason, Christopher E. ; Jasiulionis, Miriam G.
Número total de Autores: 12
Tipo de documento: Artigo Científico
Fonte: CLINICAL EPIGENETICS; v. 14, n. 1, p. 20-pg., 2022-12-01.
Resumo

The epigenetic changes associated with melanoma progression to advanced and metastatic stages are still poorly understood. To shed light on the CpG methylation dynamics during melanoma development, we analyzed the methylome profiles of a four-stage cell line model of melanoma progression: non-tumorigenic melanocytes (melan-a), premalignant melanocytes (4C), non-metastatic melanoma cells (4C11-), and metastatic melanoma cells (4C11+). We identified 540 hypo- and 37 hypermethylated gene promoters that together characterized a malignancy signature, and 646 hypo- and 520 hypermethylated promoters that distinguished a metastasis signature. Differentially methylated genes from these signatures were correlated with overall survival using TCGA-SKCM methylation data. Moreover, multivariate Cox analyses with LASSO regularization identified panels of 33 and 31 CpGs, respectively, from the malignancy and metastasis signatures that predicted poor survival. We found a concordant relationship between DNA methylation and transcriptional levels for genes from the malignancy (Pyroxd2 and Ptgfrn) and metastasis (Arnt2, Igfbp4 and Ptprf) signatures, which were both also correlated with melanoma prognosis. Altogether, this study reveals novel CpGs methylation markers associated with malignancy and metastasis that collectively could improve the survival prediction of melanoma patients. (AU)

Processo FAPESP: 19/23480-4 - Novas estratégias para eliminação de células tumorais residuais utilizando terapia epigenética
Beneficiário:Miriam Galvonas Jasiulionis
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 18/20775-0 - RNAs não codificantes envolvidos com a gênese e a progressão do melanoma
Beneficiário:Miriam Galvonas Jasiulionis
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 14/13663-0 - Integração de dados de expressão de genes e microRNAs, metiloma e hidroximetiloma de diferentes etapas da progressão do melanoma.
Beneficiário:Miriam Galvonas Jasiulionis
Modalidade de apoio: Auxílio à Pesquisa - Regular