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The highly expressed secreted phosphoprotein 1 gene in prostate cancer metastasis: a microarray-based bioinformatic analysis / 中华男科学杂志
National Journal of Andrology ; (12): 984-990, 2014.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-319582
Biblioteca responsável: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the composition, function, and regulatory mechanisms of the secreted phosphoprotein 1 (SPP1) gene in metastatic prostate cancer.</p><p><b>METHODS</b>We obtained the data about the whole genomic expression profiles on prostate cancer metastasis from the GEO database, and performed data-mining and bioinformatic analysis using BRB-Array Tools and such softwares as Protparam, MotifScan, SignalP 4.0, TMHMM, NetPhos2.0, PredictProtein, GO, KEGG, and STRING.</p><p><b>RESULTS</b>Totally, 73 co-expressed differential genes in prostate cancer metastasis were identified, 21 up-regulated and 52 down-regulated (P <0.01). Bioinformatic analysis indicated that the highly expressed SPP1 gene encoded 314 amino acids and contained 2 N-glycosylation sites, 8 casein kinase II phosphorylation sites and 3 protein kinase C phosphorylation sites, playing essential roles in extracellular matrix (ECM) binding, ossification, osteoblast differentiation, cell adhesion, PI3K-Akt signaling pathway, focal adhesion, Toll-like receptor signaling pathway, and ECM-receptor interaction.</p><p><b>CONCLUSION</b>The bioinformatic method showed a high efficiency in analyzing microarray data and revealing internal biological information. SPP1 may play an important role in prostate cancer metastasis and become a novel biomarker for the diagnosis of prostate cancer metastasis and a new target for its treatment.</p>
Assuntos
Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Neoplasias da Próstata / Transdução de Sinais / Regulação para Baixo / Química / Biologia Computacional / Secreções Corporais / Fosfatidilinositol 3-Quinases / Análise em Microsséries / Receptores Toll-Like Limite: Humanos / Masculino Idioma: Chinês Revista: National Journal of Andrology Ano de publicação: 2014 Tipo de documento: Artigo
Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Neoplasias da Próstata / Transdução de Sinais / Regulação para Baixo / Química / Biologia Computacional / Secreções Corporais / Fosfatidilinositol 3-Quinases / Análise em Microsséries / Receptores Toll-Like Limite: Humanos / Masculino Idioma: Chinês Revista: National Journal of Andrology Ano de publicação: 2014 Tipo de documento: Artigo
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