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Weighted gene co-expression network analysis identifies the prognosis-related models of left- and right-sided colon cancer

Left-sided colon cancer (LC) and right-sided colon cancer (RC) are 2 essentially different diseases, and the potential mechanisms regulating them remain unidentified. In this study, we applied weighted gene co-expression network analysis (WGCNA) to confirm a yellow module, mainly enriched in metabol...

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Autores principales: Long, Chenyan, Li, Gang, Meng, Yongsheng, Huang, Xiaoliang, Chen, Jianhong, Liu, Jungang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158920/
https://www.ncbi.nlm.nih.gov/pubmed/37144998
http://dx.doi.org/10.1097/MD.0000000000033390
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author Long, Chenyan
Li, Gang
Meng, Yongsheng
Huang, Xiaoliang
Chen, Jianhong
Liu, Jungang
author_facet Long, Chenyan
Li, Gang
Meng, Yongsheng
Huang, Xiaoliang
Chen, Jianhong
Liu, Jungang
author_sort Long, Chenyan
collection PubMed
description Left-sided colon cancer (LC) and right-sided colon cancer (RC) are 2 essentially different diseases, and the potential mechanisms regulating them remain unidentified. In this study, we applied weighted gene co-expression network analysis (WGCNA) to confirm a yellow module, mainly enriched in metabolism-related signaling pathways related to LC and RC. Based on the RNA-seq data of colon cancer in The Cancer Genome Atlas (TCGA) and GSE41258 dataset with their corresponding clinical information, a training set (TCGA: LC: n = 171; RC: n = 260) and a validation set (GSE41258: LC: n = 94; RC: n = 77) were divided. Least absolute shrinkage and selection operator (LASSO) penalized COX regression analysis identified 20 prognosis-related genes (PRGs) and helped constructed 2 risk (LC-R and RC-R) models in LC and RC, respectively. The model-based risk scores accurately performed in risk stratification for colon cancer patients. The high-risk group of the LC-R model showed associations with ECM-receptor interaction, focal adhesion, and PI3K-AKT signaling pathway. Interestingly, the low-risk group of the LC-R model showed associations with immune-related signaling pathways like antigen processing and presentation. On the other hand, the high-risk group of the RC-R model showed enrichment for cell adhesion molecules and axon guidance signaling pathways. Furthermore, we identified 20 differentially expressed PRGs between LC and RC. Our findings provide new insights into the difference between LC and RC, and uncover the potential biomarkers for the treatment of LC and RC.
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spelling pubmed-101589202023-05-05 Weighted gene co-expression network analysis identifies the prognosis-related models of left- and right-sided colon cancer Long, Chenyan Li, Gang Meng, Yongsheng Huang, Xiaoliang Chen, Jianhong Liu, Jungang Medicine (Baltimore) 5700 Left-sided colon cancer (LC) and right-sided colon cancer (RC) are 2 essentially different diseases, and the potential mechanisms regulating them remain unidentified. In this study, we applied weighted gene co-expression network analysis (WGCNA) to confirm a yellow module, mainly enriched in metabolism-related signaling pathways related to LC and RC. Based on the RNA-seq data of colon cancer in The Cancer Genome Atlas (TCGA) and GSE41258 dataset with their corresponding clinical information, a training set (TCGA: LC: n = 171; RC: n = 260) and a validation set (GSE41258: LC: n = 94; RC: n = 77) were divided. Least absolute shrinkage and selection operator (LASSO) penalized COX regression analysis identified 20 prognosis-related genes (PRGs) and helped constructed 2 risk (LC-R and RC-R) models in LC and RC, respectively. The model-based risk scores accurately performed in risk stratification for colon cancer patients. The high-risk group of the LC-R model showed associations with ECM-receptor interaction, focal adhesion, and PI3K-AKT signaling pathway. Interestingly, the low-risk group of the LC-R model showed associations with immune-related signaling pathways like antigen processing and presentation. On the other hand, the high-risk group of the RC-R model showed enrichment for cell adhesion molecules and axon guidance signaling pathways. Furthermore, we identified 20 differentially expressed PRGs between LC and RC. Our findings provide new insights into the difference between LC and RC, and uncover the potential biomarkers for the treatment of LC and RC. Lippincott Williams & Wilkins 2023-05-05 /pmc/articles/PMC10158920/ /pubmed/37144998 http://dx.doi.org/10.1097/MD.0000000000033390 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal.
spellingShingle 5700
Long, Chenyan
Li, Gang
Meng, Yongsheng
Huang, Xiaoliang
Chen, Jianhong
Liu, Jungang
Weighted gene co-expression network analysis identifies the prognosis-related models of left- and right-sided colon cancer
title Weighted gene co-expression network analysis identifies the prognosis-related models of left- and right-sided colon cancer
title_full Weighted gene co-expression network analysis identifies the prognosis-related models of left- and right-sided colon cancer
title_fullStr Weighted gene co-expression network analysis identifies the prognosis-related models of left- and right-sided colon cancer
title_full_unstemmed Weighted gene co-expression network analysis identifies the prognosis-related models of left- and right-sided colon cancer
title_short Weighted gene co-expression network analysis identifies the prognosis-related models of left- and right-sided colon cancer
title_sort weighted gene co-expression network analysis identifies the prognosis-related models of left- and right-sided colon cancer
topic 5700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158920/
https://www.ncbi.nlm.nih.gov/pubmed/37144998
http://dx.doi.org/10.1097/MD.0000000000033390
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