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The distribution of circulating microRNA and their relation to coronary disease.
Freedman, Jane E; Ercan, Bahadir; Morin, Kristine M; Liu, Ching-Ti; Tamer, Lulufer; Ayaz, Lokman; Kanadasi, Mehmet; Cicek, Dilek; Seyhan, Ali Ihsan; Akilli, Rabia Eker; Camci, Celalettin; Cengiz, Beyhan; Oztuzcu, Serdar; Tanriverdi, Kahraman.
Afiliação
  • Freedman JE; Department of Medicine, University of Massachusetts Medical School, Massachusetts, 01605, USA.
  • Ercan B; Department of Medicine, University of Massachusetts Medical School, Massachusetts, 01605, USA.
  • Morin KM; Department of Medicine, University of Massachusetts Medical School, Massachusetts, 01605, USA.
  • Liu CT; Department of Biostatistics, School of Public Health, Boston University, Boston, 02118, USA.
  • Tamer L; Department of Biochemistry, Mersin University, School of Medicine, Mersin, 33343, Turkey.
  • Ayaz L; Department of Biochemistry, Mersin University, School of Medicine, Mersin, 33343, Turkey.
  • Kanadasi M; Department of Cardiology, Cukurova University, School of Medicine, Adana, 01110, Turkey.
  • Cicek D; Department of Cardiology, Mersin University, School of Medicine, Mersin, 33343, Turkey.
  • Seyhan AI; Department of Cardiology, Mersin University, School of Medicine, Mersin, 33343, Turkey.
  • Akilli RE; Department of Cardiology, Cukurova University, School of Medicine, Adana, 01110, Turkey.
  • Camci C; Department of Oncology, Gaziantep University, School of Medicine, Gazientep, 27310, Turkey.
  • Cengiz B; Department of Physiology, Gaziantep University, School of Medicine, Gazientep, 27310, Turkey.
  • Oztuzcu S; Sahinbey Hospital Central Laboratory, Gaziantep University, Gaziantep, 27310, Turkey.
  • Tanriverdi K; Department of Medicine, University of Massachusetts Medical School, Massachusetts, 01605, USA.
F1000Res ; 1: 50, 2012.
Article em En | MEDLINE | ID: mdl-24358814
ABSTRACT

BACKGROUND:

MicroRNAs (miRNAs) are small RNAs that regulate gene expression by suppressing protein translation and may influence RNA expression. MicroRNAs are detected in extracellular locations such as plasma; however, the extent of miRNA expression in plasma its relation to cardiovascular disease is not clear and many clinical studies have utilized array-based platforms with poor reproducibility. METHODS AND

RESULTS:

Initially, to define distribution of miRNA in human blood; whole blood, platelets, mononuclear cells, plasma, and serum from 5 normal individuals were screened for 852 miRNAs using high-throughput micro-fluidic quantitative RT-PCR (qRT-PCR). In total; 609, 448, 658, 147, and 178 miRNAs were found to be expressed in moderate to high levels in whole blood, platelets, mononuclear cells, plasma, and serum, respectively, with some miRNAs uniquely expressed. To determine the cardiovascular relevance of blood miRNA expression, plasma miRNA (n=852) levels were measured in 83 patients presenting for cardiac catheterization. Eight plasma miRNAs were found to have over 2-fold increased expression in patients with significant coronary disease (≥70% stenosis) as compared to those with minimal coronary disease (less than 70% stenosis) or normal coronary arteries. Expression of miR-494, miR-490-3p, and miR-769-3p were found to have significantly different levels of expression. Using a multivariable regression model including cardiovascular risk factors and medications, hsa-miR-769-3p was found to be significantly correlated with the presence of significant coronary atherosclerosis.

CONCLUSIONS:

This study utilized a superior high-throughput qRT-PCR based method and found that miRNAs are found to be widely expressed in human blood with differences expressed between cellular and extracellular fractions. Importantly, specific miRNAs from circulating plasma are associated with the presence of significant coronary disease.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: F1000Res Ano de publicação: 2012 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: F1000Res Ano de publicação: 2012 Tipo de documento: Article País de afiliação: Estados Unidos