A novel CpG-methylation-based nomogram predicts survival in colorectal cancer

被引:9
|
作者
Wang, Xiaokang [1 ]
Wang, Danwen [2 ]
Liu, Jinfeng [1 ]
Feng, Maohui [2 ]
Wu, Xiongzhi [1 ,3 ]
机构
[1] Tianjin Med Univ Canc Inst & Hosp, Tianjins Clin Res Ctr Canc, Natl Clin Res Ctr Canc, Key Lab Canc Prevent & Therapy, Tianjin 300000, Peoples R China
[2] Wuhan Univ, Clin Med Res Ctr Peritoneal Canc Wuhan, Clin Canc Study Ctr Hubei Prov,Zhongnan Hosp, Dept Gastrointestinal Surg,Key Lab Tumor Biol Beh, Wuhan 430000, Peoples R China
[3] Tianjin Nankai Hosp, Canc Ctr, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA methylation; colorectal cancer; nomogram; prognosis; survival analysis; DNA METHYLATION; MICROSATELLITE INSTABILITY; PROGNOSTIC NOMOGRAM; GENE; PHENOTYPE; REVEALS; RECURRENCE;
D O I
10.1080/15592294.2020.1762368
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aberrant DNA methylation is significantly associated with the prognosis of patients with colorectal cancer (CRC). Therefore, the aim of this study was to develop a CpG-methylation-based nomogram for prognostic prediction in CRC. First, 378 CRC patients with methylation data from The Cancer Genome Atlas were randomly divided into training cohort (n = 249) and test cohort (n = 129). A multistep screening strategy was performed to identify six CpG sites that were significantly associated with overall survival in the training cohort. Then, Cox regression modelling was performed to construct a prognostic signature based on the candidate CpG sites. The six-CpG signature successfully separated patients into high-risk and low-risk groups in both training and test cohorts, and its performance was superior to that of previously published methylation markers (P < 0.05). Furthermore, we established a prognostic nomogram incorporating this signature, TNM stage, and age. The nomogram exhibited better prediction for overall survival in comparison with the three independent prognostic factors in the training cohort (C-index: 0.798 vs 0.620 to 0.737; P < 0.001). In the test cohort, the performance of nomogram was also superior to that of the three independent prognostic factors (C-index: 0.715 vs 0.590 to 0.665; P < 0.05). Meanwhile, the calibration curves for survival probability showed good agreement between prediction by nomogram and actual observation in both training and test cohorts. Together, the present study provides a novel CpG-methylation-based nomogram as a promising predictor for overall survival of CRC patients, which may help improve decision-making regarding the personalized treatments of patients with CRC.
引用
收藏
页码:1213 / 1227
页数:15
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