内动脉瘤循环外体衍生的LncRNA ATP1A1-AS1促进光滑肌细胞的表型切换和亡
Chao Wang1, Hong Li2, Han Zhou1
1Department of Neurosurgery, The Affiliated Hospital of Qingdao University, Qingdao, People’s Republic of China.
Aging
|May 10, 2024
概括
研究人员发现,长非编码RNA ATP1A1-AS1 在内动脉瘤 (IA) 中显著升高. 这种分子促进IA的发展,可以作为诊断标记物.
科学领域:
- 生物化学 生化学
- 分子生物学分子生物学
- 基因组学就是基因组学.
背景情况:
- 外体长非编码RNAs (LncRNAs) 涉及到脑血管疾病的发病.
- 外体LncRNAs在内动脉瘤 (IAs) 中的特定作用尚不清楚.
研究的目的:
- 研究外体LncRNAs在内动脉瘤中的表达特征和功能作用.
- 确定潜在的诊断生物标志物和IA的治疗点.
主要方法:
- 高通量测序用于识别IA患者和健康对照的血外体中的差异表达LncRNA.
- 定量实时聚合酶连锁反应 (qRT-PCR) 用于验证LncRNA表达.
- 在体外实验中评估ATP1A1-AS1对血管光滑肌细胞的功能影响.
主要成果:
- 在IA患者外体内鉴定了1303个差异表达的LncRNAs.
- 在IA中,ATP1A1-AS1是最显著上调的LncRNA.
- 在体外,ATP1A1-AS1的过度表达促进了血管光滑肌肉细胞亡,表型切换和MMP-9上调.
- 在扩展样本验证中,ATP1A1-AS1显示出高的诊断价值.
结论:
- ATP1A1-AS1是内动脉瘤病变的关键参与者.
- ATP1A1-AS1显示出作为抑制IA进展的治疗点的潜力.
- ATP1A1-AS1作为IA的有价值的临床诊断标记.
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