| Literature DB >> 30008875 |
Jianrong Zheng1,2, Wei You1, Chuanxi Zheng1, Peng Wan1, Jinquan Chen1, Xiaochun Jiang1, Zhixiang Zhu1, Zhixiong Zhang1, Anqi Gong1, Wei Li1, Jifeng Tan1, Tao Ji3, Wei Guo3, Shiquan Zhang1.
Abstract
F-box proteins are essential components of the Skp-cullin-F-box complex (a type of E3 ubiquitin ligase), and participate in cell cycle and immune responses through the ubiquitin proteasome system. F-box protein 39 (FBXO39) belongs to the F-box family, which has been reported to be associated with cancer oncogenesis and progression. The present study aimed to investigate the role of FBXO39 in osteosarcoma (OS) cell proliferation and apoptosis in vitro. It was demonstrated that U-2OS cells exhibited high expression of FBXO39 compared with HOS and SaOS-2 osteosarcoma cells. Thus, knockdown of FBXO39 was performed using lentivirus-mediated short hairpin RNA (shRNA) transfection to validate the effect of FBXO39 in U-2OS cells. Western blotting and RT-qPCR analysis were used to confirm the efficiency of infection by analyzing the expression level of FBXO39. Using Celigo-based cell counting and MTT assays, it was demonstrated that FBXO39 knockdown significantly reduced the rate of cell proliferation compared with control. Caspase 3/7 activity assays and fluorescence-activated cell sorting confirmed the induction of apoptosis in U-2OS cells following FBXO39 knockdown. In conclusion, it was demonstrated that FBXO39 knockdown may significantly inhibit proliferation and promote apoptosis of U-2OS cells. Thus, FBXO39 may serve an important role in OS progression.Entities:
Keywords: F-box protein 39; U-2OS cells; apoptosis; osteosarcoma; proliferation
Year: 2018 PMID: 30008875 PMCID: PMC6036412 DOI: 10.3892/ol.2018.8876
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967