Cargando…

Development and validation of a DNA repair gene signature for prognosis prediction in Colon Cancer

Aberrant expression of DNA repair genes (DRGs) can be related to tumor progression and clinical outcomes in colon cancer. Here, we aimed to establish a DRGs signature to identify the vital prognostic DRGs in colon cancer. Firstly, gene set enrichment analysis (GSEA) was performed to demonstrate the...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Xin, Tan, Cong, Ye, Min, Wang, Xu, Weng, Weiwei, Zhang, Meng, Ni, Shujuan, Wang, Lei, Huang, Dan, Huang, Zhaohui, Xu, Midie, Sheng, Weiqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477412/
https://www.ncbi.nlm.nih.gov/pubmed/32922534
http://dx.doi.org/10.7150/jca.46328
_version_ 1783579893915713536
author Wang, Xin
Tan, Cong
Ye, Min
Wang, Xu
Weng, Weiwei
Zhang, Meng
Ni, Shujuan
Wang, Lei
Huang, Dan
Huang, Zhaohui
Xu, Midie
Sheng, Weiqi
author_facet Wang, Xin
Tan, Cong
Ye, Min
Wang, Xu
Weng, Weiwei
Zhang, Meng
Ni, Shujuan
Wang, Lei
Huang, Dan
Huang, Zhaohui
Xu, Midie
Sheng, Weiqi
author_sort Wang, Xin
collection PubMed
description Aberrant expression of DNA repair genes (DRGs) can be related to tumor progression and clinical outcomes in colon cancer. Here, we aimed to establish a DRGs signature to identify the vital prognostic DRGs in colon cancer. Firstly, gene set enrichment analysis (GSEA) was performed to demonstrate the association between abnormal expression level of DRGs and tumorigenesis. Then, a total of 476 DRGs were obtained for detecting candidate biomarkers in randomly selected 295 cases from The Cancer Genome Atlas (TCGA) colon cancer cohort. Eleven genes were screened by LASSO Cox regression analyses to develop the prognostic model. Then, the prognostic model and the expression levels of the eleven genes were validated using the internal validation dataset (the rest 125 cases in TCGA cohort) and an external validation dataset (obtained from Gene Expression Omnibus dataset). Further analysis revealed the independent prognostic capacity of the prognostic model in relation to other clinical characteristics. The receiver operating characteristic (ROC) curve analysis confirmed the good performance of the prognostic model. Furthermore, we provided a nomogram for interpreting the clinical application of the 11-DRG signature. In conclusion, we propose a newly developed 11-DRG signature as a practical prognostic predictor for patients with colon cancer, which can facilitate the individualized counselling and treatment.
format Online
Article
Text
id pubmed-7477412
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Ivyspring International Publisher
record_format MEDLINE/PubMed
spelling pubmed-74774122020-09-11 Development and validation of a DNA repair gene signature for prognosis prediction in Colon Cancer Wang, Xin Tan, Cong Ye, Min Wang, Xu Weng, Weiwei Zhang, Meng Ni, Shujuan Wang, Lei Huang, Dan Huang, Zhaohui Xu, Midie Sheng, Weiqi J Cancer Research Paper Aberrant expression of DNA repair genes (DRGs) can be related to tumor progression and clinical outcomes in colon cancer. Here, we aimed to establish a DRGs signature to identify the vital prognostic DRGs in colon cancer. Firstly, gene set enrichment analysis (GSEA) was performed to demonstrate the association between abnormal expression level of DRGs and tumorigenesis. Then, a total of 476 DRGs were obtained for detecting candidate biomarkers in randomly selected 295 cases from The Cancer Genome Atlas (TCGA) colon cancer cohort. Eleven genes were screened by LASSO Cox regression analyses to develop the prognostic model. Then, the prognostic model and the expression levels of the eleven genes were validated using the internal validation dataset (the rest 125 cases in TCGA cohort) and an external validation dataset (obtained from Gene Expression Omnibus dataset). Further analysis revealed the independent prognostic capacity of the prognostic model in relation to other clinical characteristics. The receiver operating characteristic (ROC) curve analysis confirmed the good performance of the prognostic model. Furthermore, we provided a nomogram for interpreting the clinical application of the 11-DRG signature. In conclusion, we propose a newly developed 11-DRG signature as a practical prognostic predictor for patients with colon cancer, which can facilitate the individualized counselling and treatment. Ivyspring International Publisher 2020-08-12 /pmc/articles/PMC7477412/ /pubmed/32922534 http://dx.doi.org/10.7150/jca.46328 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Wang, Xin
Tan, Cong
Ye, Min
Wang, Xu
Weng, Weiwei
Zhang, Meng
Ni, Shujuan
Wang, Lei
Huang, Dan
Huang, Zhaohui
Xu, Midie
Sheng, Weiqi
Development and validation of a DNA repair gene signature for prognosis prediction in Colon Cancer
title Development and validation of a DNA repair gene signature for prognosis prediction in Colon Cancer
title_full Development and validation of a DNA repair gene signature for prognosis prediction in Colon Cancer
title_fullStr Development and validation of a DNA repair gene signature for prognosis prediction in Colon Cancer
title_full_unstemmed Development and validation of a DNA repair gene signature for prognosis prediction in Colon Cancer
title_short Development and validation of a DNA repair gene signature for prognosis prediction in Colon Cancer
title_sort development and validation of a dna repair gene signature for prognosis prediction in colon cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477412/
https://www.ncbi.nlm.nih.gov/pubmed/32922534
http://dx.doi.org/10.7150/jca.46328
work_keys_str_mv AT wangxin developmentandvalidationofadnarepairgenesignatureforprognosispredictionincoloncancer
AT tancong developmentandvalidationofadnarepairgenesignatureforprognosispredictionincoloncancer
AT yemin developmentandvalidationofadnarepairgenesignatureforprognosispredictionincoloncancer
AT wangxu developmentandvalidationofadnarepairgenesignatureforprognosispredictionincoloncancer
AT wengweiwei developmentandvalidationofadnarepairgenesignatureforprognosispredictionincoloncancer
AT zhangmeng developmentandvalidationofadnarepairgenesignatureforprognosispredictionincoloncancer
AT nishujuan developmentandvalidationofadnarepairgenesignatureforprognosispredictionincoloncancer
AT wanglei developmentandvalidationofadnarepairgenesignatureforprognosispredictionincoloncancer
AT huangdan developmentandvalidationofadnarepairgenesignatureforprognosispredictionincoloncancer
AT huangzhaohui developmentandvalidationofadnarepairgenesignatureforprognosispredictionincoloncancer
AT xumidie developmentandvalidationofadnarepairgenesignatureforprognosispredictionincoloncancer
AT shengweiqi developmentandvalidationofadnarepairgenesignatureforprognosispredictionincoloncancer