| Literature DB >> 26883716 |
Feng Xiong1, Keyun Liu1, Fumei Zhang1, Kaihui Sha1, Xinyuan Wang1, Xiaojuan Guo1, Ning Huang1.
Abstract
While miR-204 expression may be linked to renal cell carcinoma (RCC) progression, the detailed mechanisms remain unclear. In the present study, we demonstrated that miR-204 was differentially expressed in RCC tissues when compared with surrounding normal kidney tissues. Ectopic overexpression of miR-204 in human RCC cells suppressed cell proliferation and invasion in vitro and in vivo. Mechanism dissection revealed that miR-204 may function through RAB22A signals to inhibit RCC proliferation and invasion. Overexpression of RAB22A by oe-RAB22A was able to partially reverse the miR-204-mediated suppression of RCC tumor progression. Together, these results revealed that miR-204 suppressed RCC proliferation and invasion by directly targeting the RAB22A gene. Targeting newly identified RAB22A with miR-204 may aid in the suppression of RCC proliferation and invasion.Entities:
Mesh:
Substances:
Year: 2016 PMID: 26883716 DOI: 10.3892/or.2016.4624
Source DB: PubMed Journal: Oncol Rep ISSN: 1021-335X Impact factor: 3.906