Ma Xiaoming, Du Tao, Zhu Dingjun, Chen Xianju, Lai Yiming, Wu Wanhua, Wang Qiong, Lin Chunhao, Li Zean, Liu Leyuan, Huang Hai
Department of Urology, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, Guangdong 510120, P.R. China.
Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, Guangdong 510120, P.R. China.
Oncol Lett. 2018 Nov;16(5):6749-6755. doi: 10.3892/ol.2018.9490. Epub 2018 Sep 24.
Glioma tumor suppressor candidate region gene 1 (GLTSCR1) is associated with the progression of oligodendroglioma. However, there has been little study of GLTSCR1 in prostate cancer. In the present study, the association between the expression of GLTSCR1, and the progression and prognosis of tumors in patients with prostate cancer was assessed. An immunohistochemical analysis was performed using a human tissue microarray for GLTSCR1 at the protein expression level and the immunostaining results were evaluated against clinical variables of patients with prostate cancer. Subsequently, The Cancer Genome Atlas (TCGA) was used to validate the analysis results at the mRNA level and to study the prognostic value of GLTSCR1 in prostate cancer. Immunohistochemistry and TCGA data analysis revealed that GLTSCR1 expression in the prostate cancer tissues was significantly higher than that in the benign prostate tissues (immunoreactivity score, P=0.015; mRNA levels: cancer, 447.7±6.45 vs. benign, 343.5±4.21; P<0.001). Additionally, the increased GLTSCR1 protein expression was associated with certain clinical variables in the prostate cancer tissues, including advanced clinical stage (P<0.001), enhanced tumor invasion (P=0.003), lymph node metastasis (P=0.003) and distant metastasis (P=0.001). TCGA data revealed similar results, demonstrating that the upregulation of GLTSCR1 mRNA expression was associated with the Gleason score (P<0.001), enhanced tumor invasion (P=0.011), lymph node metastasis (P=0.001) and distant metastasis (P=0.002). Furthermore, Kaplan-Meier analysis suggested that among all patients, high GLTSCR1 expression indicated a decreased overall survival (P=0.028) and biochemical recurrence (BCR)-free survival (P=0.004), compared with patients with low GLTSCR1 expression. Finally, multivariate analysis revealed that the expression of GLTSCR1 was an independent predictor of poor BCR-free survival (P=0.049). The present study suggested that the increased expression of GLTSCR1 was associated with the progression of prostate cancer. Furthermore, GLTSCR1 may be a novel biomarker that is able to predict the clinical outcome in prostate cancer patients.
胶质瘤肿瘤抑制候选区域基因1(GLTSCR1)与少突胶质细胞瘤的进展相关。然而,关于GLTSCR1在前列腺癌中的研究甚少。在本研究中,评估了GLTSCR1表达与前列腺癌患者肿瘤进展及预后之间的关联。使用人组织芯片对GLTSCR1进行蛋白表达水平的免疫组化分析,并根据前列腺癌患者的临床变量评估免疫染色结果。随后,利用癌症基因组图谱(TCGA)在mRNA水平验证分析结果,并研究GLTSCR1在前列腺癌中的预后价值。免疫组化和TCGA数据分析显示,前列腺癌组织中GLTSCR1表达显著高于良性前列腺组织(免疫反应性评分,P = 0.015;mRNA水平:癌组织,447.7±6.45 vs. 良性组织,343.5±4.21;P < 0.001)。此外,GLTSCR1蛋白表达增加与前列腺癌组织中的某些临床变量相关,包括临床晚期(P < 0.001)、肿瘤侵袭增强(P = 0.003)、淋巴结转移(P = 0.003)和远处转移(P = 0.001)。TCGA数据显示了类似结果,表明GLTSCR1 mRNA表达上调与 Gleason评分(P < 0.001)、肿瘤侵袭增强(P = 0.011)、淋巴结转移(P = 0.001)和远处转移(P = 0.002)相关。此外,Kaplan-Meier分析表明,在所有患者中,与GLTSCR1低表达患者相比,GLTSCR1高表达表明总生存期降低(P = 0.028)和无生化复发(BCR)生存期降低(P = 0.004)。最后,多变量分析显示GLTSCR1表达是无BCR生存期差的独立预测因子(P = 0.049)。本研究表明GLTSCR1表达增加与前列腺癌进展相关。此外,GLTSCR1可能是一种能够预测前列腺癌患者临床结局的新型生物标志物。