Zhang Zhenhua, Shi Zhengyuan
Department of Anesthesiology, Danyang People's hospital, Jiangsu 212300, People's Republic of China.
Open Med (Wars). 2019 Jun 30;14:516-522. doi: 10.1515/med-2019-0057. eCollection 2019.
Pseudogenes are pivotal funtional non-coding RNAs in tumorigenesis. Cumulative evidences have shown that pituitary tumor-transforming 3, pseudogene (PTTG3P), serves as an oncogene in multiple human cancers. However, its expression pattern, biological function, and potential targets in esophageal squamous cell carcinoma (ESCC) remain unknown. Here, by quantitative real-time polymerase chain reaction (qRT-PCR) in 50 cases of ESCC, we found that the expression of PTTG3P, PTTG1 and PTTG2 in esophageal squamous cancer tissues and cell lines were significantly higher than their normal counterparts (P<0.01). Spearman correlation analysis showed that the PTTG3P expression was positively correlated with the PTTG1 and PTTG2 expression in ESCC tissue samples (P<0.05). Additionally, the high expression of PTTG3P in ESCC was significantly correlated with tumor depth, lymph node invasion and TNM stage (P<0.05). We also assessed the function of PTTG3P in vitro by gain-of-function studies. Results showed that enhanced expression of PTTG3P stimulated the migration and invasion of ESCC cells, and promoted the expression level of PTTG1 and PTTG2 in vitro. Furthermore, PTTG3P fulfilled its oncogenic functions by positively regulating its parent gene PTTG1 and PTTG2. Overall, our study indicated that PTTG3P is distinctly overexpressed and exhibited oncogenic role in a PTTG1 and PTTG2 mediated manner in ESCC.
假基因是肿瘤发生过程中关键的功能性非编码RNA。越来越多的证据表明,垂体肿瘤转化基因3假基因(PTTG3P)在多种人类癌症中作为一种癌基因发挥作用。然而,其在食管鳞状细胞癌(ESCC)中的表达模式、生物学功能及潜在靶点仍不清楚。在此,通过对50例ESCC患者进行定量实时聚合酶链反应(qRT-PCR),我们发现食管鳞状癌组织和细胞系中PTTG3P、PTTG1和PTTG2的表达明显高于其正常对应物(P<0.01)。Spearman相关性分析表明,ESCC组织样本中PTTG3P的表达与PTTG1和PTTG2的表达呈正相关(P<0.05)。此外,ESCC中PTTG3P的高表达与肿瘤深度、淋巴结浸润及TNM分期显著相关(P<0.05)。我们还通过功能获得性研究在体外评估了PTTG3P的功能。结果显示,PTTG3P表达增强刺激了ESCC细胞的迁移和侵袭,并在体外促进了PTTG1和PTTG2的表达水平。此外,PTTG3P通过正向调节其亲本基因PTTG1和PTTG2发挥其致癌功能。总体而言,我们的研究表明,PTTG3P在ESCC中明显过表达,并以PTTG1和PTTG2介导的方式发挥致癌作用。