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首页> 外文期刊>European review for medical and pharmacological sciences. >Long noncoding RNA GAS5 attenuates cardiac fibroblast proliferation in atrial fibrillation via repressing ALK5
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Long noncoding RNA GAS5 attenuates cardiac fibroblast proliferation in atrial fibrillation via repressing ALK5

机译:长度非编码RNA气体5通过抑制ALK5衰减心房颤动中的心肌成纤维细胞增殖

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摘要

OBJECTIVE: Recently, long noncoding RNAs (lncRNAs) have caught more attention for their role in the progression of many diseases. Among them, lncRNA GAS5 (Growth Inhibition Specificity 5) was studied in this research to identify how it affects the progression of atrial fibrillation (AF). PATIENTS AND METHODS: In 40 patients with AF and 30 patients with sinus rhythm (SR), the GAS5 expression of the right atrial appendage (RAA) tissues was detected by the quantitative Real Time-Polymerase Chain Reaction (qRT-PCR). Moreover, the cell proliferation assay was conducted in AC16 cells transfected with GAS5 inhibitor and mimics, respectively. Furthermore, the qRT-PCR was performed to uncover the mechanism. RESULTS: In the research, the expression of GAS5 in RAA tissues was decreased significantly in AF patients than that in SR ones. Moreover, overexpression of GAS5 inhibited cell growth in AC16 cells, while knockdown of GAS5 promoted cell growth in AC16 cells. In addition, further experiments revealed that ALK5 was a target of GAS5 and its expression in AF tissues negatively correlated to GAS5 expression. CONCLUSIONS: These results indicate that GAS5 could inhibit cell proliferation of AF via suppressing ALK5, which may offer a new vision for interpreting the mechanism of AF development.
机译:目的:近日,长期非编码RNA(LNCRNA)在许多疾病的进展中都会更加关注它们的作用。其中,在该研究中研究了LNCRNA气体5(生长抑制特异性5),以确定它如何影响心房颤动的进展(AF)。患者和方法:在40例AF和30例窦性心律(SR)患者中,通过定量实时 - 聚合酶链反应(QRT-PCR)检测右心房阑尾(RAA)组织的GAS5表达。此外,细胞增殖测定分别在用气体体积抑制剂和模拟物转染的AC16细胞中进行。此外,进行QRT-PCR以揭示机制。结果:在研究中,AF患者的RAA组织中的GAS5的表达显着降低,而不是SR患者。此外,气体5的过表达抑制AC16细胞中的细胞生长,而GAS5的敲低促进了AC16细胞中的细胞生长。另外,进一步的实验表明,ALK5是气体5的靶标,其在与气体5表达呈负相关的AF组织中的表达。结论:这些结果表明,Gas5可以通过抑制ALK5抑制AF的细胞增殖,这可能提供用于解释AF开发机制的新视觉。

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