| Literature DB >> 33664240 |
Huimin Xu1, Lingao Ju2,3,4,5, Yaoyi Xiong1, Mengxue Yu6,7,8, Fenfang Zhou1, Kaiyu Qian6,7,8,9, Gang Wang6,7,8,9, Yu Xiao1,6,7,8,9, Xinghuan Wang10,11,12.
Abstract
E3 ubiquitin ligase RNF126 (ring finger protein 126) is highly expressed in various cancers and strongly associated with tumorigenesis. However, its specific function in bladder cancer (BCa) is still debatable. Here, we found that RNF126 was significantly upregulated in BCa tissue by TCGA database, and our studies indicated that downregulation of RNF126 significantly inhibited cell proliferation and metastasis through the EGFR/PI3K/AKT signaling pathway in BCa cells. Furthermore, we identified PTEN, an inhibitor of the PI3K/AKT signaling pathway, as a novel substrate for RNF126. By co-immunoprecipitation assays, we proved that RNF126 directly interacts with PTEN. Predominantly, PTEN binds to the C-terminal containing the RING domain of RNF126. The in vivo ubiquitination assay showed that RNF126 specifically regulates PTEN stability through poly-ubiquitination. Furthermore, PTEN knockdown restored cell proliferation, metastasis, and tumor formation of BCa cells inhibited by RNF126 silencing in vitro and in vivo. In conclusion, these results identified RNF126 as an oncogene that functions through ubiquitination and degradation of PTEN in BCa.Entities:
Year: 2021 PMID: 33664240 PMCID: PMC7933351 DOI: 10.1038/s41419-021-03521-1
Source DB: PubMed Journal: Cell Death Dis Impact factor: 8.469