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Hold the MYCrophone: MYC Invades Enhancers to Control Cancer-Type Gene Programs.
MacPherson-Hawthorne, Kevin; Sears, Rosalie C.
Afiliação
  • MacPherson-Hawthorne K; Department of Molecular and Medical Genetics, Oregon Health and Science University, Portland, Oregon.
  • Sears RC; Department of Molecular and Medical Genetics, Oregon Health and Science University, Portland, Oregon.
Cancer Res ; 84(14): 2227-2228, 2024 Jul 15.
Article em En | MEDLINE | ID: mdl-38695859
ABSTRACT
MYC is an oncogenic transcription factor that binds gene promoters to facilitate oncogenic gene expression. When overexpressed, as is the case in most human cancers, MYC also invades active enhancers-cis-regulatory elements that are critical for regulating gene expression. In previous studies, the regulatory significance of MYC enhancer invasion in cancer cells has been debated. In their study published in Nature Genetics, Jakobsen and colleagues establish a new role for MYC in enhancer regions regulating cancer type-specific gene programs. Their work reveals a mechanism in which MYC cooperates with other oncogenic transcription factors to recruit epigenetic regulators to enhancers, resulting in an epigenetic "switch" that promotes enhancer activation through BRD4 and RNA polymerase II. This activity was highly cancer-type specific, highlighting gene expression programs that predicted clinical outcome in a subtype-specific manner in patients with breast cancer.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação Neoplásica da Expressão Gênica / Proteínas Proto-Oncogênicas c-myc / Elementos Facilitadores Genéticos / Neoplasias Limite: Humans Idioma: En Revista: Cancer Res Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação Neoplásica da Expressão Gênica / Proteínas Proto-Oncogênicas c-myc / Elementos Facilitadores Genéticos / Neoplasias Limite: Humans Idioma: En Revista: Cancer Res Ano de publicação: 2024 Tipo de documento: Article
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