FOXM1 and UBE2C Are Distinct Biomarkers for Non-Small Cell Lung Cancer Survival Prediction: Data-Mining Based on ONCOMINE

Ya Wang, Jiang Zhu
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Abstract

Non-small cell lung cancer (NSCLC) remains to be primary reason of tumor deaths in the past few decades. The mortality of this malignancy could be reduced by developing new prognostic biomarkers and discovering novel therapeutic biological target. Here, we studied the mRNA expression of FOX gene family and UBE2C in different types of cancer compared with normal tissue through ONCOMINE differential analysis. CCLE analysis was mined to explore the expression profiles of target genes in different tumor cells. GEPIA was used to discover the expression of target genes in different subtypes and the correlation with lung cancer stage. The prognostic values of FOXM1 and UBE2C were further investigated through Kaplan-Meier plotter analysis. It showed that FOXA1, FOXD1 and FOXM1 were dramatically high expressed in NSCLC comparing with normal lung tissues. Besides, the expression of FOXM1 was significantly associated with UBE2C. Furthermore, the overexpression of FOXM1 and UBE2C were correlated to shorter survival in lung adenocarcinoma (LAC) instead of lung squamous cell carcinoma(LSCC).Hence, we could draw a conclusion that FOXM1 and UBE2C are distinguished biomarkers and crucial prognostic indicators for lung adenocarcinoma patients.
FOXM1和UBE2C是非小细胞肺癌生存预测的独特生物标志物:基于ONCOMINE的数据挖掘
在过去的几十年里,非小细胞肺癌(NSCLC)仍然是肿瘤死亡的主要原因。通过开发新的预后生物标志物和发现新的治疗生物学靶点,可以降低这种恶性肿瘤的死亡率。本研究通过ONCOMINE差异分析,研究FOX基因家族和UBE2C mRNA在不同类型肿瘤与正常组织中的表达情况。利用CCLE分析,探索不同肿瘤细胞中靶基因的表达谱。GEPIA用于发现不同亚型靶基因的表达及其与肺癌分期的关系。通过Kaplan-Meier绘图图分析进一步研究FOXM1和UBE2C的预后价值。结果表明,与正常肺组织相比,FOXA1、FOXD1和FOXM1在NSCLC中显著高表达。此外,FOXM1的表达与UBE2C显著相关。此外,FOXM1和UBE2C的过表达与肺腺癌(LAC)而非肺鳞状细胞癌(LSCC)的生存期缩短相关。因此,我们可以得出结论,FOXM1和UBE2C是肺腺癌患者独特的生物标志物和重要的预后指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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