Xu Yun-Ji, He Hong-Jie, Wu Peng, Li Wen-Bing
Department of General Surgery, The Second Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang 421001, Hunan Province, China.
World J Gastrointest Oncol. 2023 Aug 15;15(8):1412-1423. doi: 10.4251/wjgo.v15.i8.1412.
Hepatocellular carcinoma (HCC) has very low overall survival. According to global cancer statistics, approximately 905677 new cases were reported in 2020, with at least 830180 of them being fatal. Cluster of differentiation 147 (CD147) is a novel, transmembrane glycoprotein that is expressed in a wide variety of tumor cells and plays an important role in various stages of tumor development. Based on the reports described previously, we theorize that CD147 may be used as a novel biological indicator to predict the prognosis of HCC. To study this possibility, expression profiles of CD147 and corresponding clinical data from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases were analyzed, and a hazard ratio (HR) was established.
To explore the pattern of CD147 expression and its applicability in the prognosis of HCC. To establish HRs and probability points for predicting the prognosis of HCC by correlating CD147 expression with clinical characteristics. To determine if CD147 can be a reliable biomarker in HCC prognosis.
The CD147 expression profile in HCC and corresponding clinical data were obtained from TCGA database. The expression patterns of CD147 were then validated by analyzing data from the GEO database. In addition, CD147 immunohistochemistry in HCC was obtained from the Human Protein Atlas. CD147 expression patterns and clinical characteristics in the prognosis of HCC were analyzed by accessing the UALCAN web resource. Accuracy, sensitivity, and specificity of the CD147 expression profile in predictive prognosis were determined by the time-dependent receiver operating characteristic (ROC) curves. Kaplan-Meier curves were plotted to estimate the HR of survival in HCC. Univariate and multivariate Cox regression proportional hazards analyses of CD147 expression levels and clinical characteristics as prognostic factors of HCC were performed. Nomograms were used to establish probability points and predict prognosis.
Data from TCGA and GEO databases revealed that CD147 was significantly overexpressed in HCC ( = 1.624 × 10 and = 1.2 × 10, respectively). The expression of CD147 and prognosis of HCC were significantly correlated with the clinical characteristics of HCC as per the data from the UALCAN web resource ( < 0.05). Kaplan-Meier analysis of CD147 expression in HCC revealed that the high expression groups showed poor prognosis and an HR of survival > 1 [log-rank test, = 0.000542, HR (in high expression group): 1.856, 95% confidence interval (CI): 1.308 to 2.636]. ROC curves were plotted to analyze the 1-year, 3-year, and 5-year survival rates. The area under the ROC curve values were 0.675 (95%CI: 0.611 to 0.740), 0.623 (95%CI: 0.555 to 0.692), and 0.664 (95%CI: 0.582 to 9.745), respectively. Univariate Cox analysis of CD147 expression and clinical characteristics of HCC and multivariate Cox analysis of CD147 patterns and pathological tumor-node-metastasis stage showed significant differences (univariate Cox, = 0.00013, HR: 1.424, 95%CI: 1.884 to 1.707 and = 0.00066, HR: 1.376, 95%CI: 1.145 to 1.654, respectively; multivariate Cox, = 0.00578, HR: 1.507, 95%CI: 1.126 to 2.018 and = 0.00336, HR: 1.443, 95%CI: 1.129 to 1.844, respectively). Nomograms were plotted to establish the probability points and predict prognosis. The total points ranged from 0 to 180, and the C-index value was 0.673 (95%CI: 0.600 to 1.000, < 0.01).
Overexpression of CD147 was correlated with poor prognosis in HCC. The CD147 expression profile combined with clinical characteristics can reliably predict the prognosis of HCC. CD147 can serve as a biomarker to predict the prognosis of HCC.
肝细胞癌(HCC)的总体生存率很低。根据全球癌症统计数据,2020年报告了约905677例新发病例,其中至少830180例死亡。分化簇147(CD147)是一种新型跨膜糖蛋白,在多种肿瘤细胞中表达,在肿瘤发展的各个阶段发挥重要作用。根据先前的报道,我们推测CD147可能作为一种新型生物指标来预测HCC的预后。为了研究这种可能性,分析了来自癌症基因组图谱(TCGA)和基因表达综合数据库(GEO)中CD147的表达谱及相应临床数据,并建立了风险比(HR)。
探讨CD147的表达模式及其在HCC预后中的适用性。通过将CD147表达与临床特征相关联,建立预测HCC预后的HR和概率点。确定CD147是否可作为HCC预后的可靠生物标志物。
从TCGA数据库中获取HCC中CD147的表达谱及相应临床数据。然后通过分析GEO数据库的数据验证CD147的表达模式。此外,从人类蛋白质图谱中获取HCC中CD147的免疫组化数据。通过访问UALCAN网络资源分析CD147表达模式与HCC预后的临床特征。通过时间依赖性受试者工作特征(ROC)曲线确定CD147表达谱在预测预后中的准确性、敏感性和特异性。绘制Kaplan-Meier曲线以估计HCC患者的生存HR。对CD147表达水平和临床特征作为HCC预后因素进行单因素和多因素Cox回归比例风险分析。使用列线图建立概率点并预测预后。
来自TCGA和GEO数据库的数据显示,CD147在HCC中显著过表达(分别为 = 1.624 × 10和 = 1.2 × 10)。根据UALCAN网络资源的数据,CD147的表达和HCC的预后与HCC的临床特征显著相关( < 0.05)。对HCC中CD147表达的Kaplan-Meier分析显示,高表达组预后较差,生存HR > 1[对数秩检验, = 0.000542,HR(高表达组):1.856,95%置信区间(CI):1.308至2.636]。绘制ROC曲线以分析1年、3年和5年生存率。ROC曲线下面积值分别为0.675(95%CI:0.611至0.740)、0.623(95%CI:0.555至0.692)和0.664(95%CI:0.582至9.745)。对HCC的CD147表达和临床特征进行单因素Cox分析,对CD147模式和病理肿瘤-淋巴结-转移分期进行多因素Cox分析,结果显示存在显著差异(单因素Cox, = 0.00013,HR:1.424,95%CI:1.884至1.707; = 0.00066,HR:1.376,95%CI:1.145至1.654;多因素Cox, = 0.00578,HR:1.507,95%CI:1.126至2.018; = 0.00336,HR:1.443,95%CI:1.129至1.844)。绘制列线图以建立概率点并预测预后。总积分范围为0至180,C指数值为0.673(95%CI:0.600至1.000, < 0.01)。
CD147的过表达与HCC的不良预后相关。CD147表达谱结合临床特征能够可靠地预测HCC的预后。CD147可作为预测HCC预后的生物标志物。