Feng Tianhang, Lai Chunyou, Zhong Deyuan, Luo Le, Zou Haibo, Wang Guan, Yang Qinyan, Yao Yutong, Huang Xiaolun
Department of Hepatobiliary and Pancreatic Surgery, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China.
J Gastrointest Oncol. 2022 Apr;13(2):768-779. doi: 10.21037/jgo-22-168.
This study aimed to reveal novel markers for prognostic and diagnostic prediction of hepatocellular carcinoma (HCC).
We applied The Cancer Genome Atlas (TCGA) data to screen differentially expressed genes (DEGs). We identified hub modules and genes using weighted gene co-expression network analysis (WGCNA). After verification with the GSE36376 dataset, hub genes were further identified. The expression of progestin and adipoQ receptor 4 () was confirmed in HCC by quantitative reverse transcription polymerase chain reaction (qRT-PCR) The diagnostic and prognosis value of was assessed. The expression of was verified using the GSE76427 dataset.
A total of 803 were obtained between HCC and normal tissue. Through WGCNA, 7 hub modules were screened, among which the blue module was selected to identify the hub genes associated with the HCC. After overlapping all the DEGs with 837 genes of the blue module, we obtained 466 DEGs that were defined as hub genes. Among the hub genes, 239 were related to staging. After verifying with the GSE36376 dataset, was identified as the real hub gene of HCC. The results of qRT-PCR revealed that was upregulated between HCC and normal tissue. Furthermore, was related to the diagnosis and prognosis of patients with HCC. Moreover, the GSE76427 verification results of were consistent with our integration and qRT-PCR results. Ultimately, high expression of was significantly related to cell cycle, DNA replication, and the p53 signaling pathway.
The gene may be associated with the prognosis and diagnosis of HCC
本研究旨在揭示肝细胞癌(HCC)预后和诊断预测的新标志物。
我们应用癌症基因组图谱(TCGA)数据筛选差异表达基因(DEG)。我们使用加权基因共表达网络分析(WGCNA)识别枢纽模块和基因。在用GSE36376数据集验证后,进一步鉴定枢纽基因。通过定量逆转录聚合酶链反应(qRT-PCR)在HCC中证实孕激素和脂联素Q受体4()的表达。评估了的诊断和预后价值。使用GSE76427数据集验证的表达。
在HCC和正常组织之间共获得803个。通过WGCNA,筛选出7个枢纽模块,其中选择蓝色模块来识别与HCC相关的枢纽基因。将所有DEG与蓝色模块的837个基因重叠后,我们获得了466个被定义为枢纽基因的DEG。在枢纽基因中,239个与分期相关。在用GSE36376数据集验证后,被鉴定为HCC的真正枢纽基因。qRT-PCR结果显示,在HCC和正常组织之间上调。此外,与HCC患者的诊断和预后相关。此外,的GSE76427验证结果与我们的整合和qRT-PCR结果一致。最终,的高表达与细胞周期DNA复制和p53信号通路显著相关。
基因可能与HCC的预后和诊断相关