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An Apoptosis-Related Gene Prognostic Index for Colon Cancer

Purpose: To construct an apoptosis-related gene prognostic index (ARGPI) for colon cancer, and clarify the molecular and immune characteristics of the risk subgroup as defined by the prognostic index and the benefits of adjuvant chemotherapy. Integrating the prognostic index and clinicopathological...

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Autores principales: Tang, Hanmin, Wang, Jing, Luo, Xuehui, Wang, Qi, Chen, Jie, Zhang, Xinyue, Li, Qiuting, Gao, Chengyi, Li, Yuesen, Han, Suxia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8692577/
https://www.ncbi.nlm.nih.gov/pubmed/34957118
http://dx.doi.org/10.3389/fcell.2021.790878
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author Tang, Hanmin
Wang, Jing
Luo, Xuehui
Wang, Qi
Chen, Jie
Zhang, Xinyue
Li, Qiuting
Gao, Chengyi
Li, Yuesen
Han, Suxia
author_facet Tang, Hanmin
Wang, Jing
Luo, Xuehui
Wang, Qi
Chen, Jie
Zhang, Xinyue
Li, Qiuting
Gao, Chengyi
Li, Yuesen
Han, Suxia
author_sort Tang, Hanmin
collection PubMed
description Purpose: To construct an apoptosis-related gene prognostic index (ARGPI) for colon cancer, and clarify the molecular and immune characteristics of the risk subgroup as defined by the prognostic index and the benefits of adjuvant chemotherapy. Integrating the prognostic index and clinicopathological risk factors to better evaluate the prognosis of patients with colon cancer. Methods: Based on the colon adenocarcinoma data in the TCGA database, 20 apoptosis-related hub genes were screened by weighted gene co-expression network analysis (WGCNA). Five genes constituting the prognosis model were determined by Cox regression and verified by the Gene Expression Omnibus (GEO) dataset. Then the molecular and immune characteristics of risk subgroups defined by the prognostic index and the benefits of adjuvant chemotherapy were analyzed. Finally, nomograms integrating ARGPI and four clinicopathological risk factors were used to evaluate the prognosis of patients with colon cancer. Results: The ARGPI was constructed based on the FAS, VWA5A, SPTBN2, PCK1, and TIMP1 genes. In the TCGA cohort, patients in the low-risk subgroup had a longer progression-free interval (PFI) than patients in the high-risk subgroup, which coincided with the results of the GEO cohort. The comprehensive results showed that the high-risk score was related to the enrichment of the cell cycle pathway, high mutation rate of TP53 and KRAS, high infiltration of T regulatory cells (Tregs), immunosuppressive state, and less chemotherapeutic benefit. However, low-risk scores are related to drug metabolism-related pathways, low TP53 and KRAS mutation rates, high infiltration of plasma cells, more resting CD4 memory cells and eosinophils, active immune function, and better chemotherapeutic benefits. Receiver operating characteristic curve of two-year progress prediction evaluation showed that the ARGPI had higher prognostic accuracy than TNM staging. Nomograms integrating ARGPI and clinicopathological risk factors can better evaluate the prognosis of patients with colon cancer. Conclusions: The ARGPI is a promising biomarker for determining risk of colon cancer progression, molecular and immune characteristics, and chemotherapeutic benefit. This is a reliable method to predict the prognosis of colon cancer patients. It also can assist doctors in formulating more effective treatment strategies.
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spelling pubmed-86925772021-12-23 An Apoptosis-Related Gene Prognostic Index for Colon Cancer Tang, Hanmin Wang, Jing Luo, Xuehui Wang, Qi Chen, Jie Zhang, Xinyue Li, Qiuting Gao, Chengyi Li, Yuesen Han, Suxia Front Cell Dev Biol Cell and Developmental Biology Purpose: To construct an apoptosis-related gene prognostic index (ARGPI) for colon cancer, and clarify the molecular and immune characteristics of the risk subgroup as defined by the prognostic index and the benefits of adjuvant chemotherapy. Integrating the prognostic index and clinicopathological risk factors to better evaluate the prognosis of patients with colon cancer. Methods: Based on the colon adenocarcinoma data in the TCGA database, 20 apoptosis-related hub genes were screened by weighted gene co-expression network analysis (WGCNA). Five genes constituting the prognosis model were determined by Cox regression and verified by the Gene Expression Omnibus (GEO) dataset. Then the molecular and immune characteristics of risk subgroups defined by the prognostic index and the benefits of adjuvant chemotherapy were analyzed. Finally, nomograms integrating ARGPI and four clinicopathological risk factors were used to evaluate the prognosis of patients with colon cancer. Results: The ARGPI was constructed based on the FAS, VWA5A, SPTBN2, PCK1, and TIMP1 genes. In the TCGA cohort, patients in the low-risk subgroup had a longer progression-free interval (PFI) than patients in the high-risk subgroup, which coincided with the results of the GEO cohort. The comprehensive results showed that the high-risk score was related to the enrichment of the cell cycle pathway, high mutation rate of TP53 and KRAS, high infiltration of T regulatory cells (Tregs), immunosuppressive state, and less chemotherapeutic benefit. However, low-risk scores are related to drug metabolism-related pathways, low TP53 and KRAS mutation rates, high infiltration of plasma cells, more resting CD4 memory cells and eosinophils, active immune function, and better chemotherapeutic benefits. Receiver operating characteristic curve of two-year progress prediction evaluation showed that the ARGPI had higher prognostic accuracy than TNM staging. Nomograms integrating ARGPI and clinicopathological risk factors can better evaluate the prognosis of patients with colon cancer. Conclusions: The ARGPI is a promising biomarker for determining risk of colon cancer progression, molecular and immune characteristics, and chemotherapeutic benefit. This is a reliable method to predict the prognosis of colon cancer patients. It also can assist doctors in formulating more effective treatment strategies. Frontiers Media S.A. 2021-12-08 /pmc/articles/PMC8692577/ /pubmed/34957118 http://dx.doi.org/10.3389/fcell.2021.790878 Text en Copyright © 2021 Tang, Wang, Luo, Wang, Chen, Zhang, Li, Gao, Li and Han. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Tang, Hanmin
Wang, Jing
Luo, Xuehui
Wang, Qi
Chen, Jie
Zhang, Xinyue
Li, Qiuting
Gao, Chengyi
Li, Yuesen
Han, Suxia
An Apoptosis-Related Gene Prognostic Index for Colon Cancer
title An Apoptosis-Related Gene Prognostic Index for Colon Cancer
title_full An Apoptosis-Related Gene Prognostic Index for Colon Cancer
title_fullStr An Apoptosis-Related Gene Prognostic Index for Colon Cancer
title_full_unstemmed An Apoptosis-Related Gene Prognostic Index for Colon Cancer
title_short An Apoptosis-Related Gene Prognostic Index for Colon Cancer
title_sort apoptosis-related gene prognostic index for colon cancer
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8692577/
https://www.ncbi.nlm.nih.gov/pubmed/34957118
http://dx.doi.org/10.3389/fcell.2021.790878
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