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LINC00482 sponged miR-2467-3p to promote bone metastasis of prostate cancer through activating Wnt/ß-catenin signaling pathway.
Liao, Shiyao; Fang, Xuemei; Zhou, Kai; Zhao, Tingxiao; Ji, Lichen; Zhang, Wei; Zhong, Xugang; Feng, Fabo; Lv, Jun; Kang, Yao; Zhu, Danjie.
Afiliación
  • Liao S; Department of Orthopedics, Zhejiang Provincial People's Hospital, Shangtang Road 158#, Hangzhou, Zhejiang, China.
  • Fang X; Hangzhou Medical College People's Hospital, Hangzhou, Zhejiang, China.
  • Zhou K; Department of Head and Neck Surgery, Sun Yat-sen University Cancer Center, Guangzhou, China.
  • Zhao T; State Key Laboratory of Oncology in South China, Guangzhou, Guangdong, China.
  • Ji L; The First Affiliated Hospital of Wenzhou Medical University, Nanbaixiang Street, Ouhai District, Wenzhou City, Zhejiang, China.
  • Zhang W; Department of Orthopedics, Zhejiang Provincial People's Hospital, Shangtang Road 158#, Hangzhou, Zhejiang, China.
  • Zhong X; Hangzhou Medical College People's Hospital, Hangzhou, Zhejiang, China.
  • Feng F; Department of Orthopedics, Zhejiang Provincial People's Hospital, Shangtang Road 158#, Hangzhou, Zhejiang, China.
  • Lv J; The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, China.
  • Kang Y; Department of Orthopedics, Zhejiang Provincial People's Hospital, Shangtang Road 158#, Hangzhou, Zhejiang, China.
  • Zhu D; Qingdao University, Qingdao, China.
J Bone Oncol ; 41: 100494, 2023 Aug.
Article en En | MEDLINE | ID: mdl-37575527
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/ß-catenin signaling pathway, which may be a promising therapeutic target for PCa with bone metastasis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Bone Oncol Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Bone Oncol Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos