Gu Lei, Jiang Chunhui, Xu Chunjie, Liu Ye, Zhou Hong
Department of Gastrointestinal Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Front Cell Dev Biol. 2022 Feb 23;10:828415. doi: 10.3389/fcell.2022.828415. eCollection 2022.
Colon cancer (COAD) has been identified as being among the most prevalent tumors globally and ranked the third major contributor to cancer-related mortality. COAD is a molecularly heterogeneous disease. There are great differences in clinical manifestations and prognosis among different molecular subtypes. 379 TCGA-COAD samples were divided into four subtypes: primary proliferative, with collective, crypt-like, and EMT invasion. The differences among the four subtypes were analyzed from the multidimensional perspectives of immunity, genomic variation, and prognosis. The limma package was utilized to identify differentially expressed genes (DEGs) amongst different molecular subtypes. Phenotype-related coexpressed gene modules were identified using WGCNA. The polygenic prognosis model was created utilizing the lasso Cox analysis and verified by time-dependent subject operating characteristics (ROC). There are some differences in prognosis, TMB and common gene variation, immune score, and immunotherapy/chemotherapy between proliferative and three invasive molecular subtypes. 846 differential genes (DEGs) were obtained by limma packet analysis. Differential gene analysis was utilized to screen the DEGs among distinct subtypes, which were significantly enriched in the pathways related to tumorigenesis and development. Co-expression network analysis found 46 co-expressed genes correlated with proliferative and three invasive phenotypes. Based on differentially co-expressed genes, we developed a prognostic risk model of 8-genes signature, which exhibited strong stability regardless of external and internal validation. RT-PCR experiments proved the expression of eight genes in tumor and normal samples. We have developed an eight-gene signature prognostic stratification system. Furthermore, we proposed that this classifier can serve as a molecular diagnostic tool to assess the prognosis of colon cancer patients.
结肠癌(COAD)已被确定为全球最常见的肿瘤之一,是癌症相关死亡率的第三大主要贡献因素。COAD是一种分子异质性疾病。不同分子亚型之间的临床表现和预后存在很大差异。379个TCGA-COAD样本被分为四种亚型:原发性增殖型、集合型、隐窝样型和EMT侵袭型。从免疫、基因组变异和预后的多维角度分析了四种亚型之间的差异。使用limma软件包来识别不同分子亚型之间的差异表达基因(DEG)。使用WGCNA识别与表型相关的共表达基因模块。利用套索Cox分析创建多基因预后模型,并通过时间依赖受试者工作特征(ROC)进行验证。增殖型和三种侵袭性分子亚型在预后、肿瘤突变负荷(TMB)和常见基因变异、免疫评分以及免疫治疗/化疗方面存在一些差异。通过limma软件包分析获得了846个差异基因(DEG)。利用差异基因分析筛选不同亚型之间的DEG,这些基因在与肿瘤发生和发展相关的途径中显著富集。共表达网络分析发现46个与增殖型和三种侵袭性表型相关的共表达基因。基于差异共表达基因,我们开发了一种8基因特征的预后风险模型,无论外部和内部验证,该模型都表现出很强的稳定性。RT-PCR实验证明了这八个基因在肿瘤和正常样本中的表达。我们开发了一种八基因特征预后分层系统。此外,我们提出该分类器可作为一种分子诊断工具,用于评估结肠癌患者的预后。