Pir2/Rnf144b is a potential endometrial cancer biomarker that promotes cell proliferation

被引:19
|
作者
Zhou, Qing [1 ]
Eldakhakhny, Sahar [1 ]
Conforti, Franco [2 ]
Crosgie, Emma J. [1 ]
Melino, Gerry [3 ,4 ,5 ]
Sayan, Berna S. [1 ]
机构
[1] Univ Manchester, Fac Med & Human Sci, Div Canc Sci, Manchester Canc Res Ctr, Wilmslow Rd, Manchester M20 4QL, Lancs, England
[2] Univ Southampton, Fac Med, Acad Unit Clin & Expt Sci, Southampton SO16 6YD, Hants, England
[3] Univ Leicester, Med Res Council, Toxicol Unit, Hodgkin Bldg,Lancaster Rd,POB 138, Leicester LE1 9HN, Leics, England
[4] Univ Roma Tor Vergata, IDI IRCCS, Biochem Lab, I-00133 Rome, Italy
[5] Univ Roma Tor Vergata, Dept Expt Med & Biochem Sci, I-00133 Rome, Italy
来源
CELL DEATH & DISEASE | 2018年 / 9卷
关键词
GLYCOGEN-SYNTHASE KINASE-3; ESTROGEN-RECEPTOR-ALPHA; AROMATASE INHIBITORS; PROTEIN STABILITY; HIGH-FREQUENCY; MUTATIONS; CARCINOMA; PTEN; GENE; EXPRESSION;
D O I
10.1038/s41419-018-0521-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Endometrial cancer is one of the most common gynaecological cancers in developed countries. Its incidence has increased 20% over the last decade and the death rate has increased >100% over the past two decades. Current models for prediction of prognosis and treatment response are suboptimal, and as such biomarkers to support clinical decision-making and contribute to individualised treatment are needed. In this study, we show that the E3-ubiquitin ligase PIR2/RNF144B is a potential targetable biomarker in endometrial cancer. At transcript level, it is expressed both in normal endometrium and tumour samples, but at protein level, it is expressed in tumours only. By using endometrial cancer cell lines, we demonstrated that PIR2/RNF144B is stabilised via phosphorylation downstream of GSK3 beta and this is necessary for the proliferation of endometrial cancer cells, in the absence of oestrogenic growth stimuli. Here, inactivation of GSK3 beta activity is associated with loss of PIR2/RNF144B protein and consequent inhibition of cell proliferation. Our results, therefore, substantiate PIR2/RNF144B as a novel candidate for targeted therapy in endometrial cancer.
引用
收藏
页数:10
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