circPVT1 可抑制膀胱癌的扩散并有助于预测其预后

Hongyi Zhou, Xueping Cui, Leilei Zhu, Zhuoqun Xu, Zhuo Wang, Jianfeng Shao
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引用次数: 0

摘要

背景:环状 RNA PVT1(circPVT1)在多种癌症中异常表达,但其在膀胱尿路上皮癌(BLCA)中的功能作用和临床意义仍不清楚。本研究旨在确定 circPVT1 在 BLCA 中的表达水平,并在体外和体内研究其与 BLCA 进展的功能相关性:方法:参考GEPIA、UALCAN和OncoLnc提供的数据。定量实时 PCR(qPCR)用于测量 BLCA 标本和细胞系中基因的跨国表达。免疫组化(IHC)和荧光原位杂交分析(FISH)检测了HER2扩增,皮尔逊相关分析分析了circPVT1表达与临床特征的相关性,Cox回归和K-M生存分析分析了预后因素。建立了预测预后的提名图。采用CCK-8和集落形成试验检测细胞的增殖情况,并使用裸鼠模型评估体内增殖情况,采用qPCR检测增殖相关基因的表达。circPVT1的高表达与较好的生存率和阴性HER2相关,但与年龄、性别和T期无关。敲除 circPVT1 可促进 BLCA 在体外和体内的增殖。敲除circPVT1可上调ERBB2、MKI67和PCNA的表达,下调TP53的表达,但对CCND1和CCNB1的表达无影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
circPVT1 Inhibits the Proliferation and Aids in Prediction of the Prognosis of Bladder Cancer
Background: Circular RNA PVT1 (circPVT1) is aberrantly expressed in several cancers, but its functional role and clinical relevance in bladder urothelial carcinoma (BLCA) remain unknown. This study aimed to identify the expression level of circPVT1 in BLCA and investigated its functional relevance with BLCA progression both in vitro and in vivo.
Methods: GEPIA, UALCAN, and OncoLnc were referred to presented data. Quantitative real-time PCR (qPCR) was used for the measurement of transnational expression of genes in BLCA specimens and cell lines. Immunohistochemistry (IHC) and fluorescence in situ hybridization analysis (FISH) assays were performed to detect HER2 amplification, Pearson’s correlation analysis to analyze the correlation between circPVT1 expression and clinical characteristics, Cox regression and K-M survival analyses to analyze prognostic factors. A nomogram was constructed for predicting prognosis. The proliferation of cells was measured by CCK-8 and colony formation assay, and the proliferation in vivo was evaluated using nude mouse models. qPCR was used to detect the expression of proliferation-related genes.
Results: circPVT1 was but mRNA PVT1 was not significantly overexpressed in BLCA. A high circPVT1 expression was associated with a better survival and negative HER2, but not with age, gender, and T stage. circPVT1 was an independent prognostic factor for the overall survival of BLCA patients. Knocking down circPVT1 promoted BLCA proliferation in vitro and in vivo. Knocking down circPVT1 upregulated ERBB2, MKI67, and PCNA expression and downregulated TP53 expression, but exerted no influence on CCND1 and CCNB1 expression.
Conclusion: circPVT1 is a tumor suppressor and novel prognostic biomarker for BLCA.

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