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Article

Osteoglycin knockdown promotes vascular smooth muscle cell proliferation and migration in aortic dissection via the VEGF/VEGFR2 axis

  • Authors:
    • Zanxin Wang
    • Xianmian Zhuang
    • Bailang Chen
    • Minxin Wei
  • View Affiliations / Copyright

    Affiliations: Department of Cardiac Surgery, Fuwai Hospital Chinese Academy of Medical Sciences Shenzhen, Shenzhen, Guangdong 518057, P.R. China
  • Article Number: 65
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    Published online on: November 19, 2020
       https://doi.org/10.3892/mmr.2020.11703
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Abstract

Extracellular matrix (ECM) proteins serve a major role in the pathogenesis of aortic dissection (AD). The aim of the present study was to investigate the effect of osteoglycin (OGN), an ECM proteoglycan, on aortic dissection (AD), as well as the underlying mechanism. Thoracic aortic tissues from 20 patients with AD and healthy thoracic aortic tissue from 5 patients undergoing coronary artery bypass grafting were collected to detect OGN expression levels. Following OGN knockdown in rat aortic smooth muscle cells, cell proliferation was detected by performing Cell Counting Kit‑8 and BrdU assays, cell migration was assessed by performing the wound healing assay, cell invasion was detected by performing the Transwell assay, and VEGFR/AKT signaling pathway‑related protein expression levels were measured via western blotting. The results demonstrated that OGN expression was significantly downregulated in patients with AD compared with healthy controls. Compared with the si‑negative control (NC) group, OGN knockdown promoted RASMC proliferation and migration. Compared with the si‑NC group, OGN knockdown also significantly enhanced the phosphorylation of the downstream signaling molecules of VEGFR, including AKT and ERK1/2, in VEGF‑stimulated RASMCs. Collectively, the present study indicated that OGN knockdown facilitated RASMC proliferation and migration by activating AKT and ERK1/2 signaling. Therefore, OGN may serve as a novel therapeutic target for AD.
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Copy and paste a formatted citation
Spandidos Publications style
Wang Z, Zhuang X, Chen B and Wei M: Osteoglycin knockdown promotes vascular smooth muscle cell proliferation and migration in aortic dissection via the VEGF/VEGFR2 axis. Mol Med Rep 23: 65, 2021.
APA
Wang, Z., Zhuang, X., Chen, B., & Wei, M. (2021). Osteoglycin knockdown promotes vascular smooth muscle cell proliferation and migration in aortic dissection via the VEGF/VEGFR2 axis. Molecular Medicine Reports, 23, 65. https://doi.org/10.3892/mmr.2020.11703
MLA
Wang, Z., Zhuang, X., Chen, B., Wei, M."Osteoglycin knockdown promotes vascular smooth muscle cell proliferation and migration in aortic dissection via the VEGF/VEGFR2 axis". Molecular Medicine Reports 23.1 (2021): 65.
Chicago
Wang, Z., Zhuang, X., Chen, B., Wei, M."Osteoglycin knockdown promotes vascular smooth muscle cell proliferation and migration in aortic dissection via the VEGF/VEGFR2 axis". Molecular Medicine Reports 23, no. 1 (2021): 65. https://doi.org/10.3892/mmr.2020.11703
Copy and paste a formatted citation
x
Spandidos Publications style
Wang Z, Zhuang X, Chen B and Wei M: Osteoglycin knockdown promotes vascular smooth muscle cell proliferation and migration in aortic dissection via the VEGF/VEGFR2 axis. Mol Med Rep 23: 65, 2021.
APA
Wang, Z., Zhuang, X., Chen, B., & Wei, M. (2021). Osteoglycin knockdown promotes vascular smooth muscle cell proliferation and migration in aortic dissection via the VEGF/VEGFR2 axis. Molecular Medicine Reports, 23, 65. https://doi.org/10.3892/mmr.2020.11703
MLA
Wang, Z., Zhuang, X., Chen, B., Wei, M."Osteoglycin knockdown promotes vascular smooth muscle cell proliferation and migration in aortic dissection via the VEGF/VEGFR2 axis". Molecular Medicine Reports 23.1 (2021): 65.
Chicago
Wang, Z., Zhuang, X., Chen, B., Wei, M."Osteoglycin knockdown promotes vascular smooth muscle cell proliferation and migration in aortic dissection via the VEGF/VEGFR2 axis". Molecular Medicine Reports 23, no. 1 (2021): 65. https://doi.org/10.3892/mmr.2020.11703
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