Department of Liver and Pancreatic Surgery, The Affiliated Foshan Hospital, Sun Yat-Sen University, Foshan 528000, China.
Department of Pancreatobiliary Surgery, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, China.
Aging (Albany NY). 2020 Feb 21;12(4):3431-3450. doi: 10.18632/aging.102820.
HIF-1 (hypoxia-inducible factor 1) signaling played a vital role in HCC (hepatocellular carcinoma) prognosis. We aimed to establish an accurate risk scoring system for HCC prognosis prediction and treatment guidance. 424 samples from TCGA (The Cancer Genome Atlas) and 445 samples from GSE14520 dataset were included as the derivation and validation cohort, respectively. In the derivation cohort, prognostic relevant signatures were selected from sixteen HIF-1 related genes and LASSO regression was adopted for model construction. Tumor-infiltrating immune cells were calculated using CIBERSORT algorithm. HIF-1 signaling significantly increased in HCC samples compared with normal tissues. Scoring system based on SLC2A1, ENO1, LDHA and GAPDH exhibited a continuous predictive ability for OS (overall survival) in HCC patients. PCA and t-SNE analysis confirmed a reliable clustering ability of risk score in both cohorts. Patients were classified into high-risk and low-risk groups and the survival outcomes between the two groups showed significant differences. In the derivation cohort, Cox regression indicated the scoring system was an independent predictor for OS, which was validated in the validation cohort. Different infiltrating immune cells fraction and immune scores were also observed in different groups. Herein, a novel integrated scoring system was developed based on HIF-1 related genes, which would be conducive to the precise treatment of patients.
HIF-1(缺氧诱导因子 1)信号在 HCC(肝细胞癌)预后中起着至关重要的作用。我们旨在建立一个准确的风险评分系统,用于 HCC 预后预测和治疗指导。来自 TCGA(癌症基因组图谱)的 424 个样本和 GSE14520 数据集的 445 个样本分别作为推导和验证队列。在推导队列中,从十六个 HIF-1 相关基因中选择与预后相关的特征,并采用 LASSO 回归进行模型构建。使用 CIBERSORT 算法计算肿瘤浸润免疫细胞。与正常组织相比,HIF-1 信号在 HCC 样本中显著增加。基于 SLC2A1、ENO1、LDHA 和 GAPDH 的评分系统在 HCC 患者的 OS(总生存期)中表现出连续的预测能力。PCA 和 t-SNE 分析证实了风险评分在两个队列中都具有可靠的聚类能力。患者被分为高风险和低风险组,两组之间的生存结果存在显著差异。在推导队列中,Cox 回归表明评分系统是 OS 的独立预测因子,这在验证队列中得到了验证。不同的浸润免疫细胞分数和免疫评分也在不同组中观察到。在此,基于 HIF-1 相关基因开发了一种新的综合评分系统,这将有助于患者的精确治疗。