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High levels of glioma tumor suppressor candidate region gene 1 predicts a poor prognosis for prostate cancer

机译:高水平的神经胶质瘤抑癌候选区域基因1预测前列腺癌的预后不良

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摘要

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.
机译: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有关。然而,关于前列腺癌中GLTSCR1的研究很少。在本研究中,评估了GLTSCR1的表达与前列腺癌患者肿瘤的进展和预后之间的关系。使用人类组织微阵列对GLTSCR1进行了蛋白质表达水平的免疫组织化学分析,并针对前列腺癌患者的临床变量评估了免疫染色结果。随后,使用癌症基因组图谱(TCGA)验证了mRNA水平的分析结果,并研究了GLTSCR1在前列腺癌中的预后价值。免疫组织化学和TCGA数据分析显示,前列腺癌组织中GLTSCR1的表达明显高于良性前列腺组织(免疫反应评分,P = 0.015; mRNA水平:癌症,良性447.7±6.45,良性343.5±4.21; P < 0.001)。此外,GLTSCR1蛋白表达的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),肿瘤浸润增强(P = 0.003),淋巴结转移(P = 0.003)和远处转移(P = 0.003)。 P = 0.001)。 TCGA数据显示了相似的结果,表明GLTSCR1 mRNA表达的上调与格里森评分(P <0.001),肿瘤浸润增强(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,高GLTSCR1表达与低GLTSCR1表达相比,表明总生存期降低(P = 0.028)和无生化复发(BCR)的生存期(P = 0.004)。最后,多变量分析显示,GLTSCR1的表达是不良BCR无生存期的独立预测因子(P = 0.049)。本研究表明,GLTSCR1表达的增加与前列腺癌的进展有关。此外,GLTSCR1可能是一种新型的生物标志物,能够预测前列腺癌患者的临床结局。

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