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前列腺癌中假基因相关的基因融合。

Pseudogene Associated Recurrent Gene Fusion in Prostate Cancer.

机构信息

Department of Pathology, University of Alabama at Birmingham, Birmingham, AL.

Vattikuti Urology Institute, Department of Urology, Henry Ford Health System, Detroit, MI.

出版信息

Neoplasia. 2019 Oct;21(10):989-1002. doi: 10.1016/j.neo.2019.07.010. Epub 2019 Aug 22.

Abstract

We present the functional characterization of a pseudogene associated recurrent gene fusion in prostate cancer. The fusion gene KLK4-KLKP1 is formed by the fusion of the protein coding gene KLK4 with the noncoding pseudogene KLKP1. Screening of a cohort of 659 patients (380 Caucasian American; 250 African American, and 29 patients from other races) revealed that the KLK4-KLKP1 is expressed in about 32% of prostate cancer patients. Correlative analysis with other ETS gene fusions and SPINK1 revealed a concomitant expression pattern of KLK4-KLKP1 with ERG and a mutually exclusive expression pattern with SPINK1, ETV1, ETV4, and ETV5. Development of an antibody specific to KLK4-KLKP1 fusion protein confirmed the expression of the full-length KLK4-KLKP1 protein in prostate tissues. The in vitro and in vivo functional assays to study the oncogenic properties of KLK4-KLKP1 confirmed its role in cell proliferation, cell invasion, intravasation, and tumor formation. Presence of strong ERG and AR binding sites located at the fusion junction in KLK4-KLKP1 suggests that the fusion gene is regulated by ERG and AR. Correlative analysis of clinical data showed an association of KLK4-KLKP1 with lower preoperative PSA values and in young men (<50 years) with prostate cancer. Screening of patient urine samples showed that KLK4-KLKP1 can be detected noninvasively in urine. Taken together, we present KLK4-KLKP1 as a class of pseudogene associated fusion transcript in cancer with potential applications as a biomarker for routine screening of prostate cancer.

摘要

我们介绍了与前列腺癌相关的假基因重复基因融合的功能特征。融合基因 KLK4-KLKP1 是由蛋白编码基因 KLK4 与非编码假基因 KLKP1 融合而成。对 659 名患者(380 名白种人;250 名非裔美国人,以及 29 名其他种族患者)的筛查显示,KLK4-KLKP1 在约 32%的前列腺癌患者中表达。与其他 ETS 基因融合和 SPINK1 的相关性分析表明,KLK4-KLKP1 与 ERG 具有同时表达模式,与 SPINK1、ETV1、ETV4 和 ETV5 具有相互排斥的表达模式。开发一种针对 KLK4-KLKP1 融合蛋白的特异性抗体证实了 KLK4-KLKP1 全长蛋白在前列腺组织中的表达。体外和体内功能测定研究了 KLK4-KLKP1 的致癌特性,证实其在细胞增殖、细胞侵袭、血管内渗透和肿瘤形成中的作用。位于 KLK4-KLKP1 融合连接处的强 ERG 和 AR 结合位点的存在表明,融合基因受 ERG 和 AR 的调控。临床数据分析的相关性表明,KLK4-KLKP1 与术前 PSA 值较低和 50 岁以下的年轻男性(<50 岁)前列腺癌有关。对患者尿液样本的筛查表明,KLK4-KLKP1 可在尿液中无创检测。综上所述,我们提出 KLK4-KLKP1 是一种与癌症相关的假基因融合转录本,具有作为前列腺癌常规筛查生物标志物的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9779/6713813/d58fe646e47d/gr1.jpg

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