A novel long non-coding RNA PCLN16 facilitates androgen receptor signaling in prostate cancer

被引:3
|
作者
Shi, Zhenfeng [1 ]
Chen, Jie [2 ]
Wumaner, Aikebaier [1 ]
Li, Ming [1 ]
Liang, Chengyuan [3 ]
Li, Min [4 ]
机构
[1] Peoples Hosp Xinjiang Uyghur Autonomous Reg, Dept Urol, Urumqi 830002, Xinjiang, Peoples R China
[2] Peoples Hosp Xinjiang Uyghur Autonomous Reg, Dept Radiog Ctr, Urumqi 830002, Xinjiang, Peoples R China
[3] Shaanxi Univ Sci & Technol, Dept Pharm, Xian 710021, Peoples R China
[4] Xinjiang Med Univ, Dept Pharm, 393 Xinyi Rd, Urumqi 830011, Xinjiang, Peoples R China
关键词
LncRNA; PCLN16; HIP1; Prostate cancer; RESISTANCE; SURVIVAL; THERAPY;
D O I
10.1016/j.bbrc.2020.12.043
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The prostate cancer (PCa) poses serious threat to men's health. The androgen receptor (AR) is essential for normal prostate development and prostate cancer progression. We identified a novel IncRNA PCLN16 which is significantly correlated with AR signaling during prostate cancer progression. The AR-regulated PCLN16 was abundantly over expressed in localized or metastatic prostate cancer tissues and AR-dependent cell lines. PCLN16 silence suppressed AR signaling and tumor growth. PCLN16 interacted with Huntingtin interacting protein 1 (HIP1) transcript to reduce HIP1 degradation. Therefore, PCLN16 could augment AR signaling via a novel positive feedback loop. Our experiments support an oncogenic role for PCLN16 and suggest that PCLN16 might serve as a potential target for therapeutic intervention. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:78 / 84
页数:7
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