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Hsa_circ_0001879 通过 miR-6873-5p-HDAC9 轴调控氧化型低密度脂蛋白(ox-LDL)诱导的血管内皮细胞的增殖和迁移来促进动脉粥样硬化的进展。

Hsa_circ_0001879 promotes the progression of atherosclerosis by regulating the proliferation and migration of oxidation of low density lipoprotein (ox-LDL)-induced vascular endothelial cells via the miR-6873-5p-HDAC9 axis.

机构信息

Department of Cardiology, Guangdong Provincial Hospital of Traditional Chinese Medicine; The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.

The Second Clinical College of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.

出版信息

Bioengineered. 2021 Dec;12(2):10420-10429. doi: 10.1080/21655979.2021.1997224.

DOI:10.1080/21655979.2021.1997224
PMID:34872444
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8809926/
Abstract

Atherosclerosis (AS) is a typical vascular disease. Emerging evidence has shown that circRNAs play key roles in the progression of AS, but the potential function and underlying mechanism of hsa_circ_0001879 remains unknown. We detected the expression level of hsa_circ_0001879 was determined by qRT-PCR, and the proliferation rate and migration ability of HUVECs were measured by CCK-8 assay and Transwell assay, respectively. Proliferative markers and epithelium mesenchymal transition (EMT) markers were measured through immunoblotting. A dual luciferase activity assay was performed to detect the interaction between circRNAs, miRNAs, and mRNAs. Hsa_circ_0001879 was upregulated in AS patients. Hsa_circ_0001879 inhibited the proliferation and migration ability of Human umbilical vein endothelial cells (HUVECs). Hsa_circ_0001879 directly bound to miR-6873-5p and acted as a sponge. miR-6873-5p-induced HDAC9 mRNA degradation was inhibited by hsa_circ_0001879. Hsa_circ_0001879 decreased the proliferation and migration of HUVECs by inhibiting miR-6873-5p-induced HDAC9 degradation.

摘要

动脉粥样硬化(AS)是一种典型的血管疾病。新出现的证据表明,circRNAs 在 AS 的进展中发挥着关键作用,但 hsa_circ_0001879 的潜在功能和作用机制尚不清楚。我们通过 qRT-PCR 检测 hsa_circ_0001879 的表达水平,通过 CCK-8 测定法和 Transwell 测定法分别测量 HUVECs 的增殖率和迁移能力。通过免疫印迹法测量增殖标志物和上皮间质转化(EMT)标志物。进行双荧光素酶活性测定以检测 circRNAs、miRNAs 和 mRNAs 之间的相互作用。hsa_circ_0001879 在 AS 患者中上调。hsa_circ_0001879 抑制人脐静脉内皮细胞(HUVECs)的增殖和迁移能力。hsa_circ_0001879 直接与 miR-6873-5p 结合并作为海绵。hsa_circ_0001879 抑制 miR-6873-5p 诱导的 HDAC9 mRNA 降解。hsa_circ_0001879 通过抑制 miR-6873-5p 诱导的 HDAC9 降解来降低 HUVECs 的增殖和迁移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1937/8809926/dc94714974f0/KBIE_A_1997224_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1937/8809926/5dc02a0f7c1b/KBIE_A_1997224_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1937/8809926/51636f702f01/KBIE_A_1997224_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1937/8809926/d880cd90420f/KBIE_A_1997224_F0003_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1937/8809926/3e4fa8eb64e1/KBIE_A_1997224_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1937/8809926/dc94714974f0/KBIE_A_1997224_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1937/8809926/5dc02a0f7c1b/KBIE_A_1997224_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1937/8809926/51636f702f01/KBIE_A_1997224_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1937/8809926/d880cd90420f/KBIE_A_1997224_F0003_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1937/8809926/3e4fa8eb64e1/KBIE_A_1997224_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1937/8809926/dc94714974f0/KBIE_A_1997224_F0005_OC.jpg

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