Department of Pathology, University of Alabama at Birmingham, Birmingham, AL.
Vattikuti Urology Institute, Department of Urology, Henry Ford Health System, Detroit, MI.
Neoplasia. 2019 Oct;21(10):989-1002. doi: 10.1016/j.neo.2019.07.010. Epub 2019 Aug 22.
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.
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。