内德4
泛素连接酶
生物
ERBB3型
基因敲除
泛素
癌症研究
下调和上调
癌症
癌变
细胞生长
癌细胞
表皮生长因子受体
信号转导
细胞生物学
细胞培养
生物化学
遗传学
基因
作者
Zhao Huang,B-K Choi,Kalpana Mujoo,Xuejun Fan,Montero-Julian Fa,Subhajit Mukherjee,Norah A. Owiti,Ningyan Zhang,Zhiqiang An
出处
期刊:Oncogene
[Springer Nature]
日期:2014-03-24
卷期号:34 (9): 1105-1115
被引量:70
摘要
HER3/ErbB3, a member of the epidermal growth factor receptor (EGFR) family, has a pivotal role in cancer and is emerging as a therapeutic antibody target. In this study, we identified NEDD4 (neural precursor cell expressed, developmentally downregulated 4) as a novel interaction partner and ubiquitin E3 ligase of human HER3. Using molecular and biochemical approaches, we demonstrated that the C-terminal tail of HER3 interacted with the WW domains of NEDD4 and the interaction was independent of neuregulin-1. Short hairpin RNA knockdown of NEDD4 elevated HER3 levels and resulted in increased HER3 signaling and cancer cell proliferation in vitro and in vivo. A similar inverse relationship between HER3 and NEDD4 levels was observed in prostate cancer tumor tissues. More importantly, the upregulated HER3 expression by NEDD4 knockdown sensitized cancer cells for growth inhibition by an anti-HER3 antibody. Taken together, our results suggest that low NEDD4 levels may predict activation of HER3 signaling and efficacies of anti-HER3 antibody therapies.
科研通智能强力驱动
Strongly Powered by AbleSci AI