Hedgehog signaling is a potential therapeutic target for vascular calcification
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作者:
Huang, Aoran
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China Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R ChinaChina Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R China
Huang, Aoran
[1
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Li, Lu
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China Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R ChinaChina Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R China
Li, Lu
[1
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Liu, Xiaoxu
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China Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R ChinaChina Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R China
Liu, Xiaoxu
[1
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Lian, Qiuting
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China Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R ChinaChina Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R China
Lian, Qiuting
[1
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Guo, Guangying
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China Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R ChinaChina Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R China
Guo, Guangying
[1
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Xu, Tianhua
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China Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R ChinaChina Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R China
Xu, Tianhua
[1
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Lu, Xiaomei
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China Med Univ, Coll Basic Med Sci, Dept Pathophysiol, Shenyang 110013, Peoples R ChinaChina Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R China
Lu, Xiaomei
[2
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Ma, Ling
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China Med Univ, Coll Basic Med Sci, Dept Pathophysiol, Shenyang 110013, Peoples R ChinaChina Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R China
Ma, Ling
[2
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Ma, Haiying
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China Med Univ, Coll Basic Med Sci, Dept Pathophysiol, Shenyang 110013, Peoples R ChinaChina Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R China
Ma, Haiying
[2
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Yu, Yanqiu
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China Med Univ, Coll Basic Med Sci, Dept Pathophysiol, Shenyang 110013, Peoples R China
Shenyang Engn Technol R&D Ctr Cell Therapy Co LTD, Shenyang 110169, Peoples R ChinaChina Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R China
Yu, Yanqiu
[2
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机构:
Yao, Li
[1
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机构:
[1] China Med Univ, Dept Nephrol, Hosp 1, Shenyang 110000, Peoples R China
[2] China Med Univ, Coll Basic Med Sci, Dept Pathophysiol, Shenyang 110013, Peoples R China
[3] Shenyang Engn Technol R&D Ctr Cell Therapy Co LTD, Shenyang 110169, Peoples R China
Background: Patients with chronic kidney disease (CKD) suffered from vascular calcification (VC), one major contributor for their increased mortality rate. Hedgehog (Hh) signaling plays a crucial role in physiological bone mineralization and is associated with several cardiovascular diseases. However, the molecular changes underlying VC is ill defined and it remains unclear whether Hh signaling intervention affects VC.Methods: We constructed human primary vascular smooth muscle cell (VSMC) calcification model and performed RNA sequencing. Alizarin red staining and calcium content assay were conducted to identify the occurrence of VC. Three different R packages were applied to determine differentially expressed genes (DEGs). Enrichment analysis and protein-protein interaction (PPI) network analysis were carried out to explore the biological roles of DEGs. qRT-PCR assay was then applied to validate the expression of key genes. By using Connectivity Map (CMAP) analysis, several small molecular drugs targeting these key genes were obtained, including SAG (Hedgehog signaling activator) and cyclopamine (CPN) (Hedgehog signaling inhibitor), which were subsequently used to treat VSMC.Results: Obvious Alizarin red staining and increased calcium content identified the occurrence of VC. By integrating results from three R packages, we totally obtained 166 DEGs (86 up-regulated and 80 down-regulated), which were significantly enriched in ossification, osteoblast differentiation, and Hh signaling. PPI network analysis identified 10 key genes and CMAP analysis predicted several small molecular drugs targeting these key genes including chlorphenamine, isoeugenol, CPN and phenazopyridine. Notably, our in vitro experiment showed that SAG markedly alleviated VSMC calcification, whereas CPN significantly exacerbated VC.Conclusions: Our research provided deeper insight to the pathogenesis of VC and indicated that targeting Hh signaling pathway may represent a potential and effective therapy for VC.