Jin Jingpeng, Zhou Shanshan, Li Changfeng, Xu Ruisi, Zu Lingling, You Jiacong, Zhang Bin
Endoscopy Center China-Japan Union Hospital of Jilin University, 126 Xiantai Street, Changchun 130033, China.
The First Hospital of Jilin University, 71 Xinmin Street, Changchun 130021, China.
Life Sci. 2014 Jul 11;108(1):48-53. doi: 10.1016/j.lfs.2014.05.006. Epub 2014 May 17.
Aberrant expression of microRNAs (miRNAs) results in alterations of various biological processes (e.g., cell cycle, cell differentiation, and apoptosis) and cell transformation. Altered miRNAs expression was associated with lung carcinogenesis and tumor progression. This study aimed to investigate the function and underlying molecular events of miR-517a-3p on regulation of lung cancer cell proliferation and invasion.
Transfected miR-517a-3p mimics or inhibitors into 95D and 95C cells respectively, the effects of miR-517a-3p on lung cancer cell proliferation, migration, and invasion were detected. Bioinformatics software forecasted potential target genes of miR-517a-3p and dual luciferase reporter gene system and western blot verified whether miR-517a-3p regulates FOXJ3 expression directly.
MiR-517a-3p was differentially expressed in lung cancer 95D and 95C cell lines that have different metastatic potential. Manipulation of miR-517a-3p expression changed lung cancer cell proliferation, migration and invasion capacity. MiR-517a-3p directly regulated FOXJ3 expression by binding to FOXJ3 promoter.
This study demonstrated that miR-517a-3p promoted lung cancer cell proliferation and invasion by targeting of FOXJ3 expression.
微小RNA(miRNA)的异常表达会导致各种生物学过程(如细胞周期、细胞分化和凋亡)的改变以及细胞转化。miRNA表达的改变与肺癌发生及肿瘤进展相关。本研究旨在探讨miR-517a-3p在调控肺癌细胞增殖和侵袭方面的功能及潜在分子机制。
分别将miR-517a-3p模拟物或抑制剂转染至95D和95C细胞中,检测miR-517a-3p对肺癌细胞增殖、迁移和侵袭的影响。利用生物信息学软件预测miR-517a-3p的潜在靶基因,并通过双荧光素酶报告基因系统和蛋白质印迹法验证miR-517a-3p是否直接调控FOXJ3的表达。
miR-517a-3p在具有不同转移潜能的肺癌95D和95C细胞系中存在差异表达。对miR-517a-3p表达的调控改变了肺癌细胞的增殖、迁移和侵袭能力。miR-517a-3p通过与FOXJ3启动子结合直接调控FOXJ3的表达。
本研究表明,miR-517a-3p通过靶向FOXJ3表达促进肺癌细胞增殖和侵袭。