KLF4公司
脱氮酶
癌症研究
泛素
转移
生物
乳腺癌
泛素连接酶
癌症
转录因子
癌变
遗传学
SOX2
基因
作者
Haojing Zou,Hongyan Chen,Zhuan Zhou,Yong Wan,Zhihua Liu
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2019-09-26
卷期号:467: 19-28
被引量:62
标识
DOI:10.1016/j.canlet.2019.09.012
摘要
Krüppel-like factor 4 (KLF4) is an important transcription factor implicated in a variety of essential cellular processes. Aberrant KLF4 expression is closely related to tumourigenesis and tumour progression. The rapid turnover of the KLF4 protein indicates an important role for the posttranslational modifications (PTMs) of KLF4. To date, E3 ligases mediating KLF4 ubiquitination have been widely reported, yet the deubiquitinating mechanism of KLF4 remains largely unknown. We screened a library of 65 deubiquitinating enzymes and identified ATXN3 as a deubiquitinating enzyme of KLF4. Subsequent immunoprecipitation assays confirmed that ATXN3 bound to KLF4, mediating the deubiquitination and stabilization of KLF4 protein levels. Furthermore, we demonstrated that ATXN3 promoted breast cancer cell metastasis via KLF4 in vitro and in vivo. Finally, the protein expression analysis of human breast cancer specimens demonstrated that ATXN3 significantly correlated with KLF4. High ATXN3/KLF4 expression was associated with a poor prognosis in breast cancer patients. Collectively, we identified ATXN3 as a novel deubiquitinating enzyme of KLF4, providing a new explanation for breast cancer metastasis, and proposed ATXN3 as a potential target for breast cancer metastasis treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI