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B-RafV600E inhibits sodium iodide symporter expression via regulation of DNA methyltransferase 1
Experimental & Molecular Medicine ; : e120-2014.
Artigo em Inglês | WPRIM | ID: wpr-37641
ABSTRACT
B-RafV600E mutant is found in 40-70% of papillary thyroid carcinoma (PTC) and has an important role in the pathogenesis of PTC. The sodium iodide symporter (NIS) is an integral plasma membrane glycoprotein that mediates active iodide transport into the thyroid follicular cells, and B-RafV600E has been known to be associated with the loss of NIS expression. In this study, we found that B-RafV600E inhibited NIS expression by the upregulation of its promoter methylation, and that specific regions of CpG islands of NIS promoter in B-RafV600E harboring PTC were highly methylated compared with surrounding normal tissue. Although DNA methyltransferase 3a and 3b (DNMT3a,3b) were not increased by B-RafV600E, DNMT1 expression was markedly upregulated in PTC and B-RafV600E expressing thyrocytes. Furthermore, DNMT1 expression was upregulated by B-RafV600E induced NF-kappaB activation. These results led us to conclude that NIS promoter methylation, which was induced by B-RafV600E, is one of the possible mechanisms involved in NIS downregulation in PTC.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Glândula Tireoide / Neoplasias da Glândula Tireoide / Dados de Sequência Molecular / Sequência de Bases / Carcinoma / Regulação para Baixo / Regulação Neoplásica da Expressão Gênica / Regulação para Cima / Células Cultivadas / Regiões Promotoras Genéticas Limite: Humanos Idioma: Inglês Revista: Experimental & Molecular Medicine Ano de publicação: 2014 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Glândula Tireoide / Neoplasias da Glândula Tireoide / Dados de Sequência Molecular / Sequência de Bases / Carcinoma / Regulação para Baixo / Regulação Neoplásica da Expressão Gênica / Regulação para Cima / Células Cultivadas / Regiões Promotoras Genéticas Limite: Humanos Idioma: Inglês Revista: Experimental & Molecular Medicine Ano de publicação: 2014 Tipo de documento: Artigo