Bioinformatic Analyses and Integrated Machine Learning to Predict prognosis and therapeutic response Based on E3 Ligase-Related Genes in colon cancer.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-08-19 eCollection Date: 2024-01-01 DOI:10.7150/jca.98723
Lunxi Liang, Xiao Liang, Xueke Yu, Wanting Xiang
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Abstract

Purpose: Colorectal cancer is the third most common cause of cancer death worldwide. We probed the correlations between E3 ubiquitin ligase (E3)-related genes (ERGs) and colon cancer prognosis and immune responses. Methods: Gene expression profiles and clinical data of patients with colon cancer were acquired from the TCGA, GTEx, GSE17537 and GSE29621 databases. ERGs were identified by coexpression analysis. WGCNA and differential expression analysis were subsequently conducted. Consensus clustering identified two molecular clusters. Differential analysis of the two clusters and Cox regression were then conducted. A prognostic model was constructed based on 10 machine learning algorithms and 92 algorithm combinations. The CIBERSORT, ssGSEA and TIMER algorithms were used to estimate immune infiltration. The OncoPredict algorithm and The Cancer Immunome Atlas (TCIA) predicted susceptibility to chemotherapeutic and targeted drugs and immunotherapy sensitivity. CCK-8, scratch-wound and RT‒PCR assays were subsequently conducted. Results: Two ERG-associated clusters were identified. The prognosis and immune function of patients in cluster A were superior to those of patients in cluster B. We constructed a prognostic model with perfect predictive capability and validated it in internal and external colon cancer datasets. We discovered significant discrepancies in immune infiltration and immune checkpoints between different risk groups. The group with high-risk had a reduced half-maximal inhibitory concentration (IC50) for some routine antitumor drugs and reduced susceptibility to immunotherapy. In vitro experiments demonstrated that the ectopic expression of PRELP inhibited the migration and proliferation of CRC cells. Conclusions: In summary, we identified novel molecular subtypes and developed a prognostic model, which will help a lot in the advancement of better forecasting and therapeutic approaches.

基于结肠癌 E3 连接酶相关基因的生物信息分析和综合机器学习预测预后和治疗反应
目的:结直肠癌是全球第三大常见癌症死因。我们研究了 E3 泛素连接酶(E3)相关基因(ERGs)与结肠癌预后和免疫反应之间的相关性。研究方法从TCGA、GTEx、GSE17537和GSE29621数据库获取结肠癌患者的基因表达谱和临床数据。通过共表达分析确定了ERG。随后进行了 WGCNA 和差异表达分析。共识聚类确定了两个分子群。然后对这两个群组进行了差异分析和 Cox 回归。基于 10 种机器学习算法和 92 种算法组合构建了预后模型。CIBERSORT、ssGSEA和TIMER算法用于估计免疫浸润。OncoPredict算法和癌症免疫组图谱(TCIA)预测了化疗和靶向药物的敏感性以及免疫疗法的敏感性。随后进行了 CCK-8、划痕-伤口和 RT-PCR 检测。结果显示发现了两个与ERG相关的集群。我们构建了一个具有完美预测能力的预后模型,并在内部和外部结肠癌数据集中进行了验证。我们发现,不同风险组之间的免疫浸润和免疫检查点存在明显差异。高危人群对一些常规抗肿瘤药物的半数最大抑制浓度(IC50)降低,对免疫疗法的敏感性降低。体外实验表明,异位表达 PRELP 可抑制 CRC 细胞的迁移和增殖。结论:总之,我们发现了新的分子亚型,并建立了一个预后模型,这将对更好的预测和治疗方法的发展有很大帮助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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