自噬
基因敲除
AKT3
小RNA
肺动脉
生物
癌症研究
细胞生长
环状RNA
细胞生物学
AKT1型
细胞凋亡
药理学
基因
医学
内科学
信号转导
生物化学
蛋白激酶B
作者
Xiaogang Jing,Shujun Wu,Ying Liu,Huan Wang,QingFeng Huang
出处
期刊:Bioengineered
[Taylor & Francis]
日期:2022-04-01
卷期号:13 (4): 8759-8771
被引量:25
标识
DOI:10.1080/21655979.2022.2036302
摘要
Recently, several studies have been clarified that circular RNA (circRNA) was a vital regulatory gene of pulmonary hypertension (PH). Nevertheless, the action of circRNA in PH was not yet explored. This study was to figure out the biological function and potential molecular mechanism of circSirtuin1 (SIRT1) in PH. Construction of the PH rat model and hypoxia pulmonary artery smooth muscle cells (PASMC) model was performed, and test of circSIRT1/microRNA (miR)-145-5p/protein kinase-B3 (Akt3) was conducted. The influence of the circSIRT1/miR-145-5p/Akt3 axis on the histopathology, hemodynamics with autophagy of the pulmonary artery in rats was examined. Additionally, the impact of circSIRT1/miR-145-5p/Akt3 on the proliferation, migration and apoptosis with autophagy of PASMC under hypoxic environment was also determined. The targeting of circSIRT1/miR-145-5p/Akt3 was testified. The results manifested that circSIRT1 and Akt3 were elevated in PH, while miR-145-5p was declined. Knockdown of circSIRT1 ameliorated rat PH, suppressed PASMC proliferation, migration with autophagy in hypoxic environment. CircSIRT1 competitively combined with miR-145-5p to mediate Akt3. To sum up, circSIRT1/miR-145-5p/Akt3 was supposed to perform as a prospective molecular target for the treatment of PH.
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