Xu Zhicheng, Xu Chao, Wang Qionghan, Ma Shanjin, Li Yu, Liu Shaojie, Peng Shiyuan, Tan Jidong, Zhao Xiaolong, Han Donghui, Zhang Keying, Yang Lijun
Department of Urology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
School of Basic Medicine, Fourth Military Medical University, Xi'an, China.
Front Med (Lausanne). 2022 Sep 14;9:979542. doi: 10.3389/fmed.2022.979542. eCollection 2022.
Bladder cancer patients have a high recurrence and poor survival rates worldwide. Early diagnosis and intervention are the cornerstones for favorable prognosis. However, commonly used predictive tools cannot meet clinical needs because of their insufficient accuracy.
We have developed an enhancer RNA (eRNA)-based signature to improve the prediction for bladder cancer prognosis. First, we analyzed differentially expressed eRNAs in gene expression profiles and clinical data for bladder cancer from The Cancer Genome Atlas database. Then, we constructed a risk model for prognosis of bladder cancer patients, and analyzed the correlation between this model and tumor microenvironment (TME). Finally, regulatory network of downstream genes of eRNA in the model was constructed by WGCNA and enrichment analysis, then Real-time quantitative PCR verified the differentiation of related genes between tumor and adjacent tissue.
We first constructed a risk model composed of eight eRNAs, and found the risk model could be an independent risk factor to predict the prognosis of bladder cancer. Then, the log-rank test and time-dependent ROC curve analysis shown the model has a favorable ability to predict prognosis. The eight risk eRNAs may participate in disease progression by regulating cell adhesion and invasion, and up-regulating immune checkpoints to suppress the immunity in TME. mRNA level change in related genes further validated regulatory roles of eRNAs in bladder cancer. In summary, we constructed an eRNA-based risk model and confirmed that the model could predict the prognosis of bladder cancer patients.
在全球范围内,膀胱癌患者具有高复发率和低生存率。早期诊断和干预是实现良好预后的基石。然而,由于常用预测工具准确性不足,无法满足临床需求。
我们开发了一种基于增强子RNA(eRNA)的特征来改善对膀胱癌预后的预测。首先,我们分析了来自癌症基因组图谱数据库的膀胱癌基因表达谱和临床数据中差异表达的eRNA。然后,我们构建了膀胱癌患者预后的风险模型,并分析了该模型与肿瘤微环境(TME)之间的相关性。最后,通过加权基因共表达网络分析(WGCNA)和富集分析构建了模型中eRNA下游基因的调控网络,随后实时定量PCR验证了肿瘤组织与癌旁组织中相关基因的差异。
我们首先构建了一个由8个eRNA组成的风险模型,发现该风险模型可作为预测膀胱癌预后的独立危险因素。然后,对数秩检验和时间依赖性ROC曲线分析表明该模型具有良好的预后预测能力。这8个风险eRNA可能通过调节细胞黏附与侵袭以及上调免疫检查点来抑制TME中的免疫反应,从而参与疾病进展。相关基因的mRNA水平变化进一步验证了eRNA在膀胱癌中的调控作用。总之,我们构建了基于eRNA的风险模型,并证实该模型可预测膀胱癌患者的预后。