获取途径

作者

Zhaoju Tian Shuang Cao Cheng Li Mingfang Xu Huaiqing Wei Han Yang Qiyu Sun Qikui Ren Le Zhang

作者单位

Department of Neurotic Electrophysiology, Qilu Children’s Hospital of Shandong University, Jinan, China School of Public Health, Taishan Medical University, Tai’an, China

刊名

Journal of Cellular Physiology

关键词

bladder cancer cyclin‐dependent kinase 1 long noncoding RNA plasmacytoma variant translocation 1 microRNA‐31

分类号

571

摘要

Purpose The aim of our study was to validate the sway of long noncoding RNA plasmacytoma variant translocation 1 on the metabolism and growth of bladder cancer cells by microRNA‐31 /cyclin‐dependent kinase 1 . Methods The Gene Expression Omnibus database was used for analyzing the differentially expressed lncRNA and messenger RNA in bladder cancer tissues, with the highly expressed lncRNA PVT1 and mRNA CDK1 screened out. The expression level of PVT1 was detected by quantitative reverse‐tr...更多

Purpose The aim of our study was to validate the sway of long noncoding RNA plasmacytoma variant translocation 1 on the metabolism and growth of bladder cancer cells by microRNA‐31 /cyclin‐dependent kinase 1 . Methods The Gene Expression Omnibus database was used for analyzing the differentially expressed lncRNA and messenger RNA in bladder cancer tissues, with the highly expressed lncRNA PVT1 and mRNA CDK1 screened out. The expression level of PVT1 was detected by quantitative reverse‐transcription polymerase chain reaction, cell viability by Cell Counting Kit‐8 assay, cell proliferation and scratch by 5‐bromo‐2′‐deoxyuridine assay, cell migration and invasion by transwell assays, the expression level of CDK1 by immunohistochemistry and western blot analysis, transcription factor targeting by dual‐luciferase assay, and the effect of PVT1 on bladder cancer growth by nude mice tumor formation experiment. Results LncRNA PVT1 and mRNA CDK1 had a higher expression in bladder cancer cells than that in neighboring tissues. Activity, proliferation, colony formation, migration, and invasion of bladder cancer cell were noticeably reduced by the PVT1 inhibitor than that of control group. PVT1 and CDK1 have binding sites with miR‐31. When miR‐31 decreased, CDK1 mRNA and protein levels increased in vivo experiments in nude mice. When PVT1 was downregulated, the tumor size was significantly reduced and tumor proliferation was curbed. Immunohistochemistry showed that the positive rate of CDK1 and Ki‐67 decreased and the expression of miR‐31 increased after PVT1 was inhibited. Conclusions LncRNA PVT1 was overexpressed in bladder cancer cells, and it was downregulated miR‐31 to enhance CDK1 expression and facilitate bladder cancer cells proliferation, migration, and invasion.收起

学科

【SCI学科】CELL BIOLOGY;PHYSIOLOGY 【ESI学科】MOLECULAR BIOLOGY & GENETICS

文献类型

期刊

浏览量

17