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Gene Expression Regulation by Agonist-Independent Constitutive Signaling of Melanocortin-1 Receptor
Endocrinology and Metabolism ; : 179-184, 2014.
Artigo em Inglês | WPRIM | ID: wpr-55020
ABSTRACT

BACKGROUND:

Melanocortin-1 receptor (Mc1r), a key signaling receptor for melanogenesis, has been reported to mediate migration of B16F10 melanoma cells. Interestingly, this activity appears to be a part of the constitutive signaling of Mc1r.

METHODS:

We carried out small interfering RNA-mediated knock-down of Mc1r on murine melanoma B16F10 cells and performed microarray analysis to characterize changes in the gene expression profile.

RESULTS:

We isolated 22 and four genes whose expression decreased and increased, respectively, by 2.5-fold or higher as the result of Mc1r knock-down. Several down-regulated genes have been proposed to be involved in cell migration. Among these genes are several members of the chemokine gene family.

CONCLUSION:

We provide a gene set for further functional analyses of Mc1r. The Mc1r target genes we present may be particularly relevant for understanding the ligand-independent activity of Mc1r. Further examination of the mode of action may lead to novel strategies in regulating the migration and metastasis of melanoma cells.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Movimento Celular / Regulação da Expressão Gênica / Genes vif / Quimiocinas / Receptor Tipo 1 de Melanocortina / Análise em Microsséries / Transcriptoma / Melanoma / Metástase Neoplásica Limite: Humanos Idioma: Inglês Revista: Endocrinology and Metabolism Ano de publicação: 2014 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Movimento Celular / Regulação da Expressão Gênica / Genes vif / Quimiocinas / Receptor Tipo 1 de Melanocortina / Análise em Microsséries / Transcriptoma / Melanoma / Metástase Neoplásica Limite: Humanos Idioma: Inglês Revista: Endocrinology and Metabolism Ano de publicação: 2014 Tipo de documento: Artigo