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J Med Virol ; 87(9): 1608-15, 2015 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-25879916

RESUMO

Inflammation and reactive oxygen species (ROS) production have recently considered as key mechanisms in the pathogenesis of Kaposi's sarcoma (KS). Since mitochondria are the major source of ROS production, this organelle may play a main role in KS development. However, there are no studies on mtDNA variations and haplogroups in this area. The focus of this study was to investigate the mtDNA variants and haplogroups in KS patients and their relationship to tumor development. To address this, we have genotyped mtDNA in 45 Iranian KS patients and 48 age and sex-matched Iranian controls. A strong positive correlation was observed between UK cluster and decreased risk of KS. Our results suggest that the UK cluster might be a protective haplogroup for KS development. It is probably superhaplogroup UK, with lower ATP and ROS production, may prevent KSHV reactivation from latent to lytic phase that is essential for KS development.


Assuntos
DNA Mitocondrial/genética , Genes Mitocondriais , Haplótipos , Polimorfismo Genético , Sarcoma de Kaposi/genética , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Variação Genética , Genótipo , Herpesvirus Humano 8/genética , Humanos , Irã (Geográfico) , Masculino , Pessoa de Meia-Idade , Mutação , Espécies Reativas de Oxigênio/metabolismo , Sarcoma de Kaposi/etnologia , Reino Unido
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