MicroRNA-186 targets SKP2 to induce p27(Kip1)-mediated pituitary tumor cell cycle deregulation and modulate cell proliferation
10.4196/kjpp.2019.23.3.171
- Author:
Zongze HE
1
;
Longyi CHEN
;
Qi WANG
;
Cheng YIN
;
Junting HU
;
Xiao HU
;
Fan FEI
;
Jian TANG
Author Information
1. Department of Neurosurgery, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610072, Sichuan, China. chenly11@163.com, tangjian@med.uestc.edu.cn
- Publication Type:Original Article
- Keywords:
Cell proliferation;
Cyclin-dependent kinase inhibitor p27;
microRNA-186;
Pituitary neoplasms;
S-phase kinase-interacting protein-2
- MeSH:
Animals;
Cell Cycle;
Cell Proliferation;
Cyclin-Dependent Kinase Inhibitor p27;
Genes, Reporter;
Humans;
Luciferases;
Pituitary Neoplasms;
Rats;
Up-Regulation
- From:The Korean Journal of Physiology and Pharmacology
2019;23(3):171-179
- CountryRepublic of Korea
- Language:English
-
Abstract:
Pituitary tumors are usually benign but can occasionally exhibit hormonal and proliferative behaviors. Dysregulation of the G1/S restriction point largely contributes to the over-proliferation of pituitary tumor cells. F-box protein S-phase kinase-interacting protein-2 (SKP2) reportedly targets and inhibits the expression of p27(Kip1), a well-known negative regulator of G1 cell cycle progression. In this study, SKP2 expression was found to be upregulated while p27(Kip1) expression was determined to be downregulated in rat and human pituitary tumor cells. Furthermore, SKP2 knockdown induced upregulation of p27(Kip1) and cell growth inhibition in rat and human pituitary tumor cells, while SKP2overexpression elicited opposite effects on p27(Kip1) expression and cell growth. The expression of microRNA-186 (miR-186) was reported to be reduced in pituitary tumors. Online tools predicted SKP2 to be a direct downstream target of miR-186, which was further confirmed by luciferase reporter gene assays. Moreover, miR-186 could modulate the cell proliferation and p27(Kip1)-mediated cell cycle alternation of rat and human pituitary tumor cells through SKP2. As further confirmation of these findings, miR-186 and p27(Kip1) expression were downregulated, while SKP2 expression was upregulated in human pituitary tumor tissue samples; thus, SKP2 expression negatively correlated with miR-186 and p27(Kip1) expression. In contrast, miR-186 expression positively associated with p27(Kip1) expression. Taken together, we discovered a novel mechanism by which miR-186/SKP2 axis modulates pituitary tumor cell proliferation through p27(Kip1)-mediated cell cycle alternation.
