Hypoxia activates the hypoxia-inducible factor-1α/vascular endothelial growth factor pathway in a prostatic stromal cell line: A mechanism for the pathogenesis of benign prostatic hyperplasia

被引:0
作者
Zhang, Tao [1 ]
Mao, Changlin [2 ]
Chang, Yao [1 ]
Lyu, Jiaju [1 ]
Zhao, Delong [1 ]
Ding, Sentai [1 ]
机构
[1] Shandong First Med Univ, Shandong Prov Hosp, Dept Urol, Jinan 250021, Peoples R China
[2] Fujian Med Univ, Dept Urol, Mindong Hosp, Fuan, Peoples R China
关键词
Benign prostatic hyperplasia; Hypoxia-inducible factor-1 alpha; Vascular endothelial growth factor; Pathogenesis; miR-17-5p; FACTOR VEGF; HIF-1-ALPHA; EXPRESSION; MARKERS;
D O I
10.1097/CU9.0000000000000233
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
BackgroundThe development of benign prostatic hyperplasia (BPH) is closely related to hypoxia in the prostatic stroma, and the hypoxia-inducible factor-1 alpha/vascular endothelial growth factor (HIF-1 alpha/VEGF) pathway has been shown to significantly activate in response to hypoxia. The underlying mechanism for activation of this pathway in the pathogenesis of BPH remains unclear.Materials and methodsWe constructed HIF-1 alpha overexpression and knockdown BPH stromal (WPMY-1) and epithelial (BPH-1) cell lines, which were cultured under different oxygen conditions (hypoxia, normoxia, and hypoxia + HIF-1 alpha inhibitor). Quantitative real-time polymerase chain reaction (qPCR) and Western blotting were applied to detect the expression of the HIF-1 alpha/VEGF pathway. Cell proliferation and apoptosis were analyzed by Cell Counting Kit-8 and flow cytometry. We used the miRWalk 2.0 database and Western blotting to predict the potential miRNA that selectively targets the HIF-1 alpha/VEGF pathway, and verified the prediction by qPCR and dual-luciferase assays.ResultsIn a BPH stromal cell line (WPMY-1), the expression of VEGF was in accordance with HIF-1 alpha levels, elevated in the overexpression cells and decreased in the knockdown cells. Hypoxia-induced HIF-1 alpha overexpression, which could be reversed by a HIF-1 alpha inhibitor. Moreover, the HIF-1 alpha inhibitor significantly depressed cellular proliferation and promoted apoptosis in hypoxic conditions, assessed by Cell Counting Kit-8 and flow cytometry. However, in the BPH epithelial cell line (BPH-1), the expression level of HIF-1 alpha did not influence the expression of VEGF. Finally, a potential miRNA, miR-17-5p, regulating the HIF-1 alpha/VEGF pathway was predicted from the miRWalk 2.0 database and Western blotting, and verified by qPCR and dual-luciferase assay.ConclusionsIn hypoxia, activation of the HIF-1 alpha/VEGF pathway plays a crucial role in regulating cell proliferation in a BPH stromal cell line. Regulation by miR-17-5p may be the potential mechanism for the activation of this pathway. Regulation of this pathway may be involved in the pathogenesis of BPH.
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页码:185 / 193
页数:9
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