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Provedor de dados:  Genet. Mol. Biol.
País:  Brazil
Título:  Association of long non-coding RNA MIAT and MALAT1 expression profiles in peripheral blood of coronary artery disease patients with previous cardiac events
Autores:  Toraih,Eman A.
El-Wazir,Aya
Alghamdi,Saleh A.
Alhazmi,Ayman S
El-Wazir,Mohammad
Abdel-Daim,Mohamed M.
Fawzy,Manal S.
Data:  2019-09-01
Ano:  2019
Palavras-chave:  CAD
LncRNA
MALAT1
MIAT
Real-time qPCR
Resumo:  Abstract Long non-coding RNAs (lncRNAs) are implicated in various cellular and pathological processes. Two lncRNAs, myocardial infarction-associated transcript (MIAT) and metastasis-associated lung adenocarcinoma transcript 1 (MALAT1), may be involved in the pathogenesis of coronary artery disease (CAD). Here, we aimed to determine the relative circulating levels of MIAT and MALAT1 in 110 stable CAD patients and 117 controls and to correlate their levels with the clinical and laboratory data. Peripheral blood expression levels were quantified by Real-Time qPCR. The median MIAT expression level in CAD patients was significantly 12-fold higher than controls (p<0.001). Otherwise, the median MALAT1 expression level was comparable in patient and control groups. Both lncRNAs showed significantly higher relative expression levels in patients with positive history of previous cardiac ischemic events, and MIAT showed significantly higher expression in diabetic CAD patients. The area under the curve of MIAT (0.888 ± 0.02 with sensitivity 95.5% and specificity 72.7%), was significantly larger than that of MALAT1 (0.601 ± 0.04 with sensitivity 50% and specificity 63.6%) for detecting the presence of significant CAD. The current findings suggest that lncRNA MIAT could have a diagnostic significance in CAD patients. MALAT1 levels, however, are not sufficiently reliable to have much clinical use in our cases.
Tipo:  Info:eu-repo/semantics/article
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572019000400509
Editor:  Sociedade Brasileira de Genética
Relação:  10.1590/1678-4685-gmb-2018-0185
Formato:  text/html
Fonte:  Genetics and Molecular Biology v.42 n.3 2019
Direitos:  info:eu-repo/semantics/openAccess
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