Research Center for Human Tissue and Organs Degeneration, Institute of Biomedicine and Biotechnology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Department of Respiratory Medicine, People's Hospital of Longhua, The Affiliated Hospital of Southern Medical University, Shenzhen, China.
Pathol Oncol Res. 2022 Aug 25;28:1610199. doi: 10.3389/pore.2022.1610199. eCollection 2022.
The heterogeneity of hepatocellular carcinoma (HCC) highlights the importance of precision therapy. In recent years, single-cell RNA sequencing has been used to reveal the expression of genes at the single-cell level and comprehensively study cell heterogeneity. This study combined big data analytics and single-cell data mining to study the influence of genes on HCC prognosis. The cells and genes closely related to the HCC were screened through single-cell RNA sequencing (71,915 cells, including 34,414 tumor cells) and big data analysis. Comprehensive bioinformatics analysis of the key genes of HCC was conducted for molecular classification and multi-dimensional correlation analyses, and a prognostic model for HCC was established. Finally, the correlation between the prognostic model and clinicopathological features was analyzed. 16,880 specific cells, screened from the single-cell expression profile matrix, were divided into 20 sub-clusters. Cell typing revealed that 97% of these cells corresponded to HCC cell lines, demonstrating the high specificity of cells derived from single-cell sequencing. 2,038 genes with high variability were obtained. The 371 HCC samples were divided into two molecular clusters. Cluster 1 (C1) was associated with tumorigenesis, high immune score, immunotherapy targets (PD-L1 and CYLA-4), high pathological stage, and poor prognosis. Cluster 2 (C2) was related to metabolic and immune function, low immune score, low pathological stage, and good prognosis. Seven differentially expressed genes (CYP3A4, NR1I2, CYP2C9, TTR, APOC3, CYP1A2, and AFP) identified between the two molecular clusters were used to construct a prognostic model. We further validated the correlation between the seven key genes and clinical features, and the established prognostic model could effectively predict HCC prognosis. Our study identified seven key genes related to HCC that were used to construct a prognostic model through single-cell sequencing and big data analytics. This study provides new insights for further research on clinical targets of HCC and new biomarkers for clinical application.
肝细胞癌 (HCC) 的异质性突出了精准治疗的重要性。近年来,单细胞 RNA 测序被用于揭示单细胞水平的基因表达,并全面研究细胞异质性。本研究结合大数据分析和单细胞数据挖掘,研究基因对 HCC 预后的影响。通过单细胞 RNA 测序(71915 个细胞,包括 34414 个肿瘤细胞)和大数据分析筛选与 HCC 密切相关的细胞和基因。对 HCC 的关键基因进行全面的生物信息学分析,进行分子分类和多维相关分析,并建立 HCC 的预后模型。最后,分析了预后模型与临床病理特征的相关性。从单细胞表达谱矩阵中筛选出 16880 个特异细胞,分为 20 个子群。细胞分型表明,这些细胞中 97%对应于 HCC 细胞系,证明了单细胞测序获得的细胞特异性高。得到 2038 个具有高变异性的基因。371 个 HCC 样本分为两个分子簇。簇 1 (C1) 与肿瘤发生、高免疫评分、免疫治疗靶点(PD-L1 和 CYLA-4)、高病理分期和不良预后相关。簇 2 (C2) 与代谢和免疫功能相关,免疫评分低,病理分期低,预后良好。在两个分子簇之间鉴定出 7 个差异表达基因 (CYP3A4、NR1I2、CYP2C9、TTR、APOC3、CYP1A2 和 AFP),用于构建预后模型。我们进一步验证了这 7 个关键基因与临床特征的相关性,所建立的预后模型能有效预测 HCC 预后。本研究通过单细胞测序和大数据分析,确定了与 HCC 相关的 7 个关键基因,用于构建预后模型。本研究为进一步研究 HCC 的临床靶点和临床应用的新生物标志物提供了新的见解。