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circAFF1 Aggravates Vascular Endothelial Cell Dysfunction Mediated by miR-516b/SAV1/YAP1 Axis
Hong-Guang Wang1,2,3,4, Hua Yan2,3, Chen Wang3,5
1College of Pharmacy, Nankai University, Tianjin, China.
Frontiers in Physiology
|August 28, 2020
Summary
Hypoxia-induced circular RNA AFF1 (circAFF1) activates SAV1/YAP1, causing vascular endothelial dysfunction. This circAFF1/miR-516b/SAV1/YAP1 pathway may serve as an early diagnostic marker for vascular diseases.
Area of Science:
- Molecular Biology
- Vascular Biology
- Biochemistry
Background:
- Hypoxia-induced vascular endothelial damage underlies many vascular diseases.
- The role of circular RNAs in hypoxic vascular injury remains largely unknown.
Purpose of the Study:
- To investigate the role of circular RNA AFF1 (circAFF1) in hypoxic vascular injury.
- To elucidate the underlying molecular mechanism involving the SAV1/YAP1 pathway.
- To assess the potential diagnostic value of circAFF1 in related diseases.
Main Methods:
- Induction of hypoxia in HUV-EC-C and HBEC-5i cells using CoCl2.
- Quantitative analysis of circAFF1 expression.
- Assessment of cell proliferation, tube formation, and migration.
- Investigation of the circAFF1/miR-516b/SAV1/YAP1 interaction.
Main Results:
- circAFF1 was significantly upregulated under hypoxic conditions.
- Abnormal circAFF1 expression inhibited vascular endothelial cell proliferation, tube formation, and migration.
- circAFF1 acts by sequestering miR-516b, leading to SAV1 release and YAP1 phosphorylation.
- circAFF1 was found to be upregulated in patients with subarachnoid hemorrhage.
Conclusions:
- circAFF1 plays a critical role in hypoxia-induced vascular endothelial dysfunction.
- The circAFF1/miR-516b/SAV1/YAP1 axis is a key pathway in this process.
- circAFF1 demonstrates potential as an early diagnostic biomarker for hypoxia-related vascular diseases.
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