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circEZH2 是 miR363/miR708 的双重抑制剂,可促进 EZH2 表达和前列腺癌进展。

circEZH2 is a dual suppressor of miR363/miR708 to promote EZH2 expression and prostate cancer progression.

机构信息

Department of Pathology and State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, China.

Department of Thyroid and Parathyroid Surgery, West China Hospital of Sichuan University, Chengdu, China.

出版信息

Cancer Sci. 2023 Apr;114(4):1378-1395. doi: 10.1111/cas.15694. Epub 2022 Dec 28.

DOI:10.1111/cas.15694
PMID:36519785
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10067432/
Abstract

The histone methyltransferase enhancer of zeste homolog 2 (EZH2) is overexpressed in a variety of malignancies including prostate cancer (PCa) and may play important roles in tumor progression. Gene copy number gains, enhanced transcription, and a few circRNAs have been reported to upregulate EZH2. It was not known whether EZH2 itself generates circRNAs that promote its own expression. We here report the identification of circEZH2 that is derived from exons 2 and 3 of the EZH2 gene and overexpressed in PCa. We show that circEZH2 functions as a dual inhibitor for both miR363 and miR708 that target the EZH2 3'UTR and CDS, respectively, resulting in the upregulation of EZH2 expression and hence the downregulation of EZH2-repressed genes (e.g., CDH1 and DAB2IP), and enhancement of PCa cell proliferation, migration, invasion, and xenograft PCa growth. Overexpression of circEZH2 is significantly correlated with higher tumor grade, tumor progression, and unfavorable progression-free and disease-specific survival in PCa patients. These findings show a novel autoenhancing EZH2-circEZH2 -miR363/miR708-EZH2 regulatory loop, by which circEZH2 plays important roles in PCa tumorigenesis and progression by upregulating EZH2, and may have potential diagnostic, prognostic, and therapeutic uses in PCa management.

摘要

增强子结合锌指蛋白 2 (EZH2)在多种恶性肿瘤中过表达,包括前列腺癌(PCa),并且可能在肿瘤进展中发挥重要作用。已经报道了基因拷贝数增加、转录增强以及一些 circRNAs 上调 EZH2。尚不清楚 EZH2 本身是否会产生促进其自身表达的 circRNAs。我们在此报告了circEZH2 的鉴定,该 circEZH2 来自 EZH2 基因的外显子 2 和 3,在 PCa 中过表达。我们表明 circEZH2 作为 miR363 和 miR708 的双重抑制剂发挥作用,分别靶向 EZH2 3'UTR 和 CDS,导致 EZH2 表达上调,从而导致 EZH2 抑制基因(例如 CDH1 和 DAB2IP)下调,以及增强 PCa 细胞增殖、迁移、侵袭和异种移植 PCa 生长。circEZH2 的过表达与 PCa 患者更高的肿瘤分级、肿瘤进展以及不利的无进展生存期和疾病特异性生存期显著相关。这些发现表明了一种新型的 EZH2-circEZH2 -miR363/miR708-EZH2 自我增强调节环路,通过该环路,circEZH2 通过上调 EZH2 在 PCa 发生和进展中发挥重要作用,并且在 PCa 管理中具有潜在的诊断、预后和治疗用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b26/10067432/e330fabd70d9/CAS-114-1378-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b26/10067432/08f68da2d295/CAS-114-1378-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b26/10067432/7cc70dc70eda/CAS-114-1378-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b26/10067432/97edd666b941/CAS-114-1378-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b26/10067432/e330fabd70d9/CAS-114-1378-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b26/10067432/622cd37852bd/CAS-114-1378-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b26/10067432/a060ae244cb2/CAS-114-1378-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b26/10067432/a06acff6e611/CAS-114-1378-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b26/10067432/7e5b16b9c9c1/CAS-114-1378-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b26/10067432/08f68da2d295/CAS-114-1378-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b26/10067432/7cc70dc70eda/CAS-114-1378-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b26/10067432/97edd666b941/CAS-114-1378-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b26/10067432/e330fabd70d9/CAS-114-1378-g001.jpg

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