Huang Wan-Ying, Chen Gang, Chen Shang-Wei, Dang Yi-Wu, Deng Yun, Zhou Hua-Fu, Kong Jin-Liang, Zhang Yu, Mo Jun-Xian, Li Chang-Bo, He Juan
Department of Pathology, The First Affiliated Hospital of Guangxi Medical University, No. 6, Shuangyong Road, Nanning, Guangxi, China.
Department of Cardio-Thoracic Surgery, The First Affiliated Hospital of Guangxi Medical University, No. 6, Shuangyong Road, Nanning, Guangxi, China.
J Oncol. 2021 Aug 30;2021:9910962. doi: 10.1155/2021/9910962. eCollection 2021.
The purpose of this study is to investigate the significance of alpha-enolase (ENO1) expression in squamous cell carcinoma of the lung (LUSC), its prognostic value, and prospective molecular mechanism. Using multiplatforms data, including in-house immunohistochemistry, in-house real-time fluorescence quantitative polymerase chain reaction (RT-qPCR), in-house microarray, and public high-throughput data, the expression significance and prognostic role of ENO1 in LUSC tissues were analyzed comprehensively. With the combination of all eligible cases, compared with 941 non-LUSC lung tissues, ENO1 was significantly overexpressed in 1163 cases of LUSC (standardized mean difference (SMD) = 1.23, 95% confidence interval (CI) = 0.76-1.70, < 0.001). ENO1 also displayed a great ability to differentiate LUSC tissues from non-LUSC lung tissues (AUC = 0.8705) with the comprehensive sensitivity being 0.88 [0.83-0.92], and comprehensive specificity being 0.89 [0.84-0.94]). Moreover, in 1860 cases of LUSC with survival information, patients with higher expression of ENO1 had poorer prognosis (hazard ratio (HR) = 1.20, 95% CI = 1.01-1.43, = 0.043). ENO1 and its related genes mainly participated in the pathways of cell division and proliferation. In conclusion, the upregulation of ENO1 could affect the carcinogenesis and unfavorable outcome of LUSC.
本研究旨在探讨α-烯醇化酶(ENO1)在肺鳞状细胞癌(LUSC)中的表达意义、预后价值及潜在分子机制。利用多平台数据,包括内部免疫组织化学、内部实时荧光定量聚合酶链反应(RT-qPCR)、内部微阵列以及公开的高通量数据,全面分析了ENO1在LUSC组织中的表达意义及预后作用。综合所有符合条件的病例,与941例非LUSC肺组织相比,ENO1在1163例LUSC中显著高表达(标准化均值差(SMD)=1.23,95%置信区间(CI)=0.76 - 1.70,P<0.001)。ENO1在区分LUSC组织与非LUSC肺组织方面也具有很强的能力(曲线下面积(AUC)=0.8705),综合敏感性为0.88[0.83 - 0.92],综合特异性为0.89[0.84 - 0.94])。此外,在1860例有生存信息的LUSC病例中,ENO1表达较高的患者预后较差(风险比(HR)=1.20,95%CI=1.01 - 1.43,P=0.043)。ENO1及其相关基因主要参与细胞分裂和增殖途径。总之,ENO1的上调可能影响LUSC的发生发展及不良预后。