Improving the overall survival prognosis prediction accuracy: A 9‐gene signature in CRC patients

Abstract Colorectal cancer (CRC) is a malignant tumor and morbidity rates are among the highest in the world. The variation in CRC patients' prognosis prompts an urgent need for new molecular biomarkers to improve the accuracy for predicting the CRC patients' prognosis or as a complement t...

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Main Authors: Wenbo Zheng, Yijia Lu, Xiaochuang Feng, Chunzhao Yang, Ling Qiu, Haijun Deng, Qi Xue, Kai Sun
Format: Article
Language:English
Published: Wiley 2021-09-01
Series:Cancer Medicine
Subjects:
CRC
Online Access:https://doi.org/10.1002/cam4.4104
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spelling doaj-aea8412f3bc342ae909124900ba05dca2021-09-06T09:17:13ZengWileyCancer Medicine2045-76342021-09-0110175998600910.1002/cam4.4104Improving the overall survival prognosis prediction accuracy: A 9‐gene signature in CRC patientsWenbo Zheng0Yijia Lu1Xiaochuang Feng2Chunzhao Yang3Ling Qiu4Haijun Deng5Qi Xue6Kai Sun7Department of General Surgery & Guangdong Province Key Laboratory of Precision Medicine for Gastrointestinal Tumor The First School of Clinical Medicine Nanfang HospitalSouthern Medical University Guangzhou ChinaDepartment of Obstetrics and Gynaecology Nanfang HospitalSouthern Medical University Guangzhou ChinaDepartment of General Surgery & Guangdong Province Key Laboratory of Precision Medicine for Gastrointestinal Tumor The First School of Clinical Medicine Nanfang HospitalSouthern Medical University Guangzhou ChinaDepartment of General Surgery & Guangdong Province Key Laboratory of Precision Medicine for Gastrointestinal Tumor The First School of Clinical Medicine Nanfang HospitalSouthern Medical University Guangzhou ChinaDepartment of General Surgery & Guangdong Province Key Laboratory of Precision Medicine for Gastrointestinal Tumor The First School of Clinical Medicine Nanfang HospitalSouthern Medical University Guangzhou ChinaDepartment of General Surgery & Guangdong Province Key Laboratory of Precision Medicine for Gastrointestinal Tumor The First School of Clinical Medicine Nanfang HospitalSouthern Medical University Guangzhou ChinaDepartment of General Surgery Traditional Chinese and Western Medicine HospitalSouthern Medical University Guangzhou ChinaDepartment of General Surgery & Guangdong Province Key Laboratory of Precision Medicine for Gastrointestinal Tumor The First School of Clinical Medicine Nanfang HospitalSouthern Medical University Guangzhou ChinaAbstract Colorectal cancer (CRC) is a malignant tumor and morbidity rates are among the highest in the world. The variation in CRC patients' prognosis prompts an urgent need for new molecular biomarkers to improve the accuracy for predicting the CRC patients' prognosis or as a complement to the traditional TNM staging for clinical practice. CRC patients' gene expression data of HTSeq‐FPKM and matching clinical information were downloaded from The Cancer Genome Atlas (TCGA) datasets. Patients were randomly divided into a training dataset and a test dataset. By univariate and multivariate Cox regression survival analyses and Lasso regression analysis, a prediction model which divided each patient into high‐or low‐risk group was constructed. The differences in survival time between the two groups were compared by the Kaplan–Meier method and the log‐rank test. The weighted gene co‐expression network analysis (WGCNA) was used to explore the relationship between all the survival‐related genes. The survival outcomes of patients whose overall survival (OS) time were significantly lower in the high‐risk group than that in the low‐risk group both in the training and test datasets. Areas under the ROC curves which termed AUC values of our 9‐gene signature achieved 0.823 in the training dataset and 0.806 in the test dataset. A nomogram was constructed for clinical practice when we combined the 9‐gene signature with TNM stage and age to evaluate the survival time of patients with CRC, and the C‐index increased from 0.739 to 0.794. In conclusion, we identified nine novel biomarkers that not only are independent prognostic indexes for CRC patients but also can serve as a good supplement to traditional clinicopathological factors to more accurately evaluate the survival of CRC patients.https://doi.org/10.1002/cam4.4104CRCnomogramprognosissurvival‐related genesWGCNA
collection DOAJ
language English
format Article
sources DOAJ
author Wenbo Zheng
Yijia Lu
Xiaochuang Feng
Chunzhao Yang
Ling Qiu
Haijun Deng
Qi Xue
Kai Sun
spellingShingle Wenbo Zheng
Yijia Lu
Xiaochuang Feng
Chunzhao Yang
Ling Qiu
Haijun Deng
Qi Xue
Kai Sun
Improving the overall survival prognosis prediction accuracy: A 9‐gene signature in CRC patients
Cancer Medicine
CRC
nomogram
prognosis
survival‐related genes
WGCNA
author_facet Wenbo Zheng
Yijia Lu
Xiaochuang Feng
Chunzhao Yang
Ling Qiu
Haijun Deng
Qi Xue
Kai Sun
author_sort Wenbo Zheng
title Improving the overall survival prognosis prediction accuracy: A 9‐gene signature in CRC patients
title_short Improving the overall survival prognosis prediction accuracy: A 9‐gene signature in CRC patients
title_full Improving the overall survival prognosis prediction accuracy: A 9‐gene signature in CRC patients
title_fullStr Improving the overall survival prognosis prediction accuracy: A 9‐gene signature in CRC patients
title_full_unstemmed Improving the overall survival prognosis prediction accuracy: A 9‐gene signature in CRC patients
title_sort improving the overall survival prognosis prediction accuracy: a 9‐gene signature in crc patients
publisher Wiley
series Cancer Medicine
issn 2045-7634
publishDate 2021-09-01
description Abstract Colorectal cancer (CRC) is a malignant tumor and morbidity rates are among the highest in the world. The variation in CRC patients' prognosis prompts an urgent need for new molecular biomarkers to improve the accuracy for predicting the CRC patients' prognosis or as a complement to the traditional TNM staging for clinical practice. CRC patients' gene expression data of HTSeq‐FPKM and matching clinical information were downloaded from The Cancer Genome Atlas (TCGA) datasets. Patients were randomly divided into a training dataset and a test dataset. By univariate and multivariate Cox regression survival analyses and Lasso regression analysis, a prediction model which divided each patient into high‐or low‐risk group was constructed. The differences in survival time between the two groups were compared by the Kaplan–Meier method and the log‐rank test. The weighted gene co‐expression network analysis (WGCNA) was used to explore the relationship between all the survival‐related genes. The survival outcomes of patients whose overall survival (OS) time were significantly lower in the high‐risk group than that in the low‐risk group both in the training and test datasets. Areas under the ROC curves which termed AUC values of our 9‐gene signature achieved 0.823 in the training dataset and 0.806 in the test dataset. A nomogram was constructed for clinical practice when we combined the 9‐gene signature with TNM stage and age to evaluate the survival time of patients with CRC, and the C‐index increased from 0.739 to 0.794. In conclusion, we identified nine novel biomarkers that not only are independent prognostic indexes for CRC patients but also can serve as a good supplement to traditional clinicopathological factors to more accurately evaluate the survival of CRC patients.
topic CRC
nomogram
prognosis
survival‐related genes
WGCNA
url https://doi.org/10.1002/cam4.4104
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