PO.MCB07.04 · 分子与细胞生物学

USP21在前列腺癌中的作用

The role of USP21 in prostate cancer

海报缩略图:USP21在前列腺癌中的作用
编号 7359 展板 16 时间 4/22 09:00–12:00 区域 Section 24 主讲 Cheng Zhang, PhD
分会场 Transcription Factor Function in Cell Identity, Signaling, and Post-Transcriptional Control
查看 PDF 下载 PDF 🔒 查看 / 下载完整 PDF 需登录并开通下载套餐 · 查看套餐 / 开通 AACR 官方页面

作者与单位 Authors & Affiliations

Cheng Zhang

University of Kentucky, Lexington, KY

摘要 Abstract

中文摘要
泛素特异性蛋白酶21(USP21)是一种去泛素化酶,在多种癌症中具有促癌作用。而其在前列腺癌中的作用和分子机制仍不明确。为研究USP21在促进前列腺癌中的作用,我们评估发现USP21在前列腺癌患者中mRNA表达最高,且高USP21水平预示前列腺癌患者预后不良。此外,抑制USP21显著抑制前列腺癌细胞增殖。在体内,USP21缺失在异种移植模型中显著抑制肿瘤生长。此外,我们通过串联亲和纯化鉴定出雄激素受体(AR)为USP21的潜在底物。机制上,i)USP21通过对AR的K48连接多聚泛素化进行去泛素化,直接与AR相互作用并使其稳定,而AR是前列腺癌的主要驱动因素。沉默USP21增强AR的多聚泛素化,促进其蛋白酶体降解,并最终减弱PSA,而重新引入AR可在很大程度上恢复这些效应。ii)根据我们的RNA-seq研究,USP21调控AR的转录活性,我们揭示siUSP21降低雄激素反应和AR诱导的通路,且敲低USP21降低AR靶基因的mRNA水平。总之,我们的项目深入揭示了USP21调控AR以促进前列腺癌进展的机制,从而为前列腺癌治疗提供了一种新途径。
查看英文原文 English abstract
The Ubiquitin-specific protease 21 (USP21) is a deubiquitinase with pro-carcinogenic effects in various cancers. While its role and molecular mechanism in prostate cancer remain elusive. To investigate the role of USP21 in promoting prostate cancer, we evaluated that USP21 shows the highest mRNA expression in prostate cancer patients, and high USP21 levels predicted a poor prognosis in patients with prostate cancer. Additionally, suppression of USP21 significantly inhibited prostate cancer cell proliferation. In vivo , USP21 depletion significantly suppressed tumor growth in xenograft models. Moreover, we identified the androgen receptor (AR) as a potential substrate of USP21 by tandem affinity purification. Mechanistically, i) USP21 directly interacted and stabilized AR by deubiquitinating its K48-linked polyubiquitination, which is a main driver for prostate cancer. Silencing of USP21 enhances polyubiquitination of AR, promotes its proteasomal degradation, and ultimately attenuates PSA, while these effects could be largely restored by reintroduction of AR. ii) USP21 regulates transcriptional activity of AR according to our RNA-seq studies, we revealed that siUSP21 decreases both androgen response and AR-induced pathways, and knockdown USP21 decreases mRNA level of AR target genes. In conclusion, our project gives insight into the mechanism underlying how USP21 regulates AR to promote the progression of prostate cancer , therefore providing a novel approach for prostate cancer treatment.
利益披露 Disclosure
C. Zhang, None.

← 返回 AACR 2026 检索