Yang Guangda, Xiao Jieming, He Huixiang, Wang Jing, Wang Zhichao, Jian Liumeng, Chen Qianya
Department of Cancer Chemotherapy, The Fourth Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511300, People's Republic of China.
Department of Emergency, The Fourth Affiliated Hospital of Guangzhou Medical University, Guangzhou, 511300, People's Republic of China.
Immunotargets Ther. 2025 Aug 25;14:931-952. doi: 10.2147/ITT.S532644. eCollection 2025.
Colorectal cancer (CRC) is a major cause of cancer deaths globally, mainly due to treatment resistance. Neddylation, a key post-translational modification, is linked to tumor growth and immune response, offering potential therapeutic targets, though its role in CRC is not well-explored.
We examined neddylation-related genes (NRGs) across cell subtypes using CRC scRNA-seq data from the TISCH database. Unsupervised clustering of TCGA and GEO bulk RNA-seq data identified various neddylation patterns. A neddylation-related gene signature (NRGS) was developed using ten machine-learning algorithms and validated externally. The study compared biofunctions, including functional analysis, immune cell infiltration, genomic mutations, enrichment analysis, and responses to immunotherapy and chemotherapy, between high- and low-risk groups defined by the NRGS model.
scRNA-seq analysis showed that the high neddylation score group had more malignant and diverse immune and stromal cells, with activated pathways aiding tumor growth and spread. We identified two neddylation patterns: Cluster A and Cluster B. Cluster B, associated with worse survival, had more immunosuppressive cells and increased tumor progression. We developed a neddylation-related gene signature (NRGS) using ten machine-learning algorithms, which accurately predicted outcomes. Higher risk scores correlated with poorer survival, with AUCs of 0.979, 0.989, and 0.996 for 1-year, 2-year, and 3-year OS in the training cohort. The NRGS was linked to higher recurrence or metastasis, advanced disease stage, and independently predicted OS risk. Patients with high NRGS may resist immunotherapy and standard chemotherapy.
The NRGS could predict outcomes and responses to immunotherapy and chemotherapy in CRC patients, aiding personalized treatment, though further validation is needed.
结直肠癌(CRC)是全球癌症死亡的主要原因,主要是由于治疗耐药性。Neddylation是一种关键的翻译后修饰,与肿瘤生长和免疫反应有关,提供了潜在的治疗靶点,但其在CRC中的作用尚未得到充分研究。
我们使用来自TISCH数据库的CRC单细胞RNA测序(scRNA-seq)数据检查了不同细胞亚型中的Neddylation相关基因(NRGs)。对TCGA和GEO批量RNA-seq数据进行无监督聚类,确定了各种Neddylation模式。使用十种机器学习算法开发了一种Neddylation相关基因特征(NRGS)并进行了外部验证。该研究比较了由NRGS模型定义的高风险和低风险组之间的生物功能,包括功能分析、免疫细胞浸润、基因组突变、富集分析以及对免疫治疗和化疗的反应。
scRNA-seq分析表明,高Neddylation评分组具有更多恶性且多样的免疫和基质细胞,其激活的通路有助于肿瘤生长和扩散。我们确定了两种Neddylation模式:A簇和B簇。与较差生存相关的B簇具有更多免疫抑制细胞且肿瘤进展增加。我们使用十种机器学习算法开发了一种Neddylation相关基因特征(NRGS),其能准确预测结果。较高风险评分与较差生存相关,训练队列中1年、2年和3年总生存期(OS)的曲线下面积(AUC)分别为0.979、0.989和0.996。NRGS与更高复发或转移、晚期疾病阶段相关,并独立预测OS风险。NRGS高的患者可能对免疫治疗和标准化疗耐药。
NRGS可以预测CRC患者的预后以及对免疫治疗和化疗的反应,有助于个性化治疗,不过仍需要进一步验证。