Liu Qian, Deng Junjie, Wei Xundong, Yuan Wei, Ma Jie
Department of Colorectal Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
J Cell Biochem. 2019 Jul;120(7):11256-11264. doi: 10.1002/jcb.28403. Epub 2019 Feb 12.
Colorectal cancer (CRC) is a common malignant tumor with high morbidity and mortality around the world. The aim of this study was to determine the genes significantly associated with the overall survival (OS) of CRC patients and predict their function in the competing endogenous RNA (ceRNA) regulation networks. We constructed the lncRNA-miRNA-mRNA networks according to the differentially expressed RNAs from the The Cancer Genome Atlas data sets of 561 CRC patients. Twelve differentially expressed messenger RNAs from the ceRNA networks were selected through a univariate Cox proportional hazards regression. Then, these genes were analyzed by using multivariate Cox proportional hazards stepwise regression to construct a prognostic model in which five genes (tensin 1, clusterin, proteolipid protein 1, epiregulin, and transcription factor Spi-B) were included. The Kaplan-Meier risk survival analysis showed that this five-gene signature independently predicted a 5-year overall survival in CRC patients (P < 0.001). Furthermore, significance was verified according to two irrelevant Gene Expression Omnibus (GEO) data sets (GSE38832 and GSE39582). The verified five-gene model of CRC can be used to predict patient prognosis and will inform postoperational evaluation and follow-up strategies.
结直肠癌(CRC)是一种在全球范围内发病率和死亡率都很高的常见恶性肿瘤。本研究的目的是确定与CRC患者总生存期(OS)显著相关的基因,并预测它们在竞争性内源性RNA(ceRNA)调控网络中的功能。我们根据来自561例CRC患者的癌症基因组图谱数据集的差异表达RNA构建了lncRNA-miRNA-mRNA网络。通过单变量Cox比例风险回归从ceRNA网络中筛选出12个差异表达的信使RNA。然后,使用多变量Cox比例风险逐步回归对这些基因进行分析,以构建一个包含五个基因(张力蛋白1、聚集素、蛋白脂质蛋白1、表皮调节素和转录因子Spi-B)的预后模型。Kaplan-Meier风险生存分析表明,这个五基因特征能够独立预测CRC患者的5年总生存期(P < 0.001)。此外,根据两个不相关的基因表达综合数据库(GEO)数据集(GSE38832和GSE39582)验证了其显著性。经验证的CRC五基因模型可用于预测患者预后,并为术后评估和随访策略提供参考。