LINC00482 sponged miR-2467-3p to promote bone metastasis of prostate cancer through activating Wnt/β-catenin signaling pathway

被引:3
|
作者
Liao, Shiyao [1 ,2 ]
Fang, Xuemei [7 ,8 ]
Zhou, Kai [3 ]
Zhao, Tingxiao [1 ,2 ]
Ji, Lichen [1 ,4 ,5 ]
Zhang, Wei [1 ,6 ]
Zhong, Xugang [1 ,6 ]
Feng, Fabo [1 ,2 ]
Lv, Jun [1 ,2 ]
Kang, Yao [1 ,2 ]
Zhu, Danjie [1 ,2 ]
机构
[1] Zhejiang Prov Peoples Hosp, Dept Orthoped, Shangtang Rd 158, Hangzhou, Zhejiang, Peoples R China
[2] Peoples Hosp, Hangzhou Med Coll, Hangzhou, Zhejiang, Peoples R China
[3] Wenzhou Med Univ, Affiliated Hosp 1, Nanbaixiang St, Wenzhou, Zhejiang, Peoples R China
[4] Wenzhou Med Univ, Affiliated Hosp 2, Wenzhou, Peoples R China
[5] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou, Peoples R China
[6] Qingdao Univ, Qingdao, Peoples R China
[7] Sun Yat Sen Univ, Canc Ctr, Dept Head & Neck Surg, Guangzhou, Peoples R China
[8] State Key Lab Oncol South China, Guangzhou, Guangdong, Peoples R China
关键词
LINC00482; miR-2467-3p; Wnt/beta-catenin; Prostate cancer; Bone metastasis; LONG NONCODING RNA; PROGRESSION; MICRORNAS; CERNA;
D O I
10.1016/j.jbo.2023.100494
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study was designed to investigate the biological functions of LINC00482 in prostate cancer (PCa) with bone metastasis. TCGA dataset of PCa was applied for LINC00482 expression analysis and real time PCR was used to verify the expression level of LINC00482 in PCa tissues as well as PCa bone metastatic tissues. To detect the biological functions of LINC00482 in vitro, various assays were used including CCK-8, EdU, colony formation and transwell assays. The biological functions of LINC00482 were also identified in vivo by inoculating PCa cells into the left cardiac ventricle of mice, followed by evaluating the osteolytic lesions and osteolytic score. In addition, Starbase and Lncbase databases were applied for predicting the potential target miRNA of LINC00482, while TargetScan and Starbase databases were used for predicting the potential target of miRNA. The luciferase reporter assay was utilized to determine the interactions among these molecules and western blotting was employed to verified the targeted proteins. Results showed that high expression level of LINC00482 was observed in bone metastatic PCa tissues and associated with PCa progression. Silencing of LINC00482 inhibited cell proliferation, migration and invasion in PCa. Furthermore, LINC00482 was proved to act as a competing endogenous RNA by sponging miR-2467-3p to activate Wnt/beta-catenin signaling pathway, which may be a promising therapeutic target for PCa with bone metastasis.
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页数:11
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