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Six Genes Associated with Lymphatic Metastasis in Colon Adenocarcinoma Linked to Prognostic Value and Tumor Immune Cell Infiltration

OBJECTIVE: The aim of the study is to explore the relationship between lymphatic metastasis genes, prognosis, and immune cell infiltration in patients with colon cancer. METHODS: Based on the Cancer Genome Atlas Program (TCGA) database, differentially expressed genes and prognostic genes related to...

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Autores principales: Wang, Baoquan, Yin, Changjun, Yang, Xu, Shi, Huibo, Zhang, Zheng, Zhou, Jun, Zhang, Peitong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444393/
https://www.ncbi.nlm.nih.gov/pubmed/36072412
http://dx.doi.org/10.1155/2022/4304361
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author Wang, Baoquan
Yin, Changjun
Yang, Xu
Shi, Huibo
Zhang, Zheng
Zhou, Jun
Zhang, Peitong
author_facet Wang, Baoquan
Yin, Changjun
Yang, Xu
Shi, Huibo
Zhang, Zheng
Zhou, Jun
Zhang, Peitong
author_sort Wang, Baoquan
collection PubMed
description OBJECTIVE: The aim of the study is to explore the relationship between lymphatic metastasis genes, prognosis, and immune cell infiltration in patients with colon cancer. METHODS: Based on the Cancer Genome Atlas Program (TCGA) database, differentially expressed genes and prognostic genes related to colon adenocarcinoma (COAD) lymphatic metastasis were screened and intersected. We used lasso and univariate Cox regression analysis to screen core genes and establish a preliminary prediction model. GO and KEGG enrichment analysis was used for lymphatic metastasis-related genes, and single GSEA was used for the final screening results. Finally, we evaluated the relationship between identified genes and immune cell infiltration. RESULTS: A total of 1727 genes were differentially expressed between COAD patients with TNM stages of N0 and N1. After further screening, six core genes (RNU4-2, ZNF556, RNVU1-15, NSA2P6, RN7SL767P, and RN7SL473P) were obtained, and a preliminary prediction model was established, in which ZNF556 was a risk factor, and the rest were protective factors. Single GSEA showed that pathways such as systemic lupus erythematosus might play an important role in the initial lymphatic metastasis of COAD. GO and KEGG enrichment analysis of 1727 genes supported this result. Immune infiltration analysis showed that six genes were significantly correlated with T cell and NK cell families. CONCLUSION: Six core genes may affect COAD initial lymphatic metastasis through the systemic lupus erythematosus pathway and immune cell infiltration.
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spelling pubmed-94443932022-09-06 Six Genes Associated with Lymphatic Metastasis in Colon Adenocarcinoma Linked to Prognostic Value and Tumor Immune Cell Infiltration Wang, Baoquan Yin, Changjun Yang, Xu Shi, Huibo Zhang, Zheng Zhou, Jun Zhang, Peitong Evid Based Complement Alternat Med Research Article OBJECTIVE: The aim of the study is to explore the relationship between lymphatic metastasis genes, prognosis, and immune cell infiltration in patients with colon cancer. METHODS: Based on the Cancer Genome Atlas Program (TCGA) database, differentially expressed genes and prognostic genes related to colon adenocarcinoma (COAD) lymphatic metastasis were screened and intersected. We used lasso and univariate Cox regression analysis to screen core genes and establish a preliminary prediction model. GO and KEGG enrichment analysis was used for lymphatic metastasis-related genes, and single GSEA was used for the final screening results. Finally, we evaluated the relationship between identified genes and immune cell infiltration. RESULTS: A total of 1727 genes were differentially expressed between COAD patients with TNM stages of N0 and N1. After further screening, six core genes (RNU4-2, ZNF556, RNVU1-15, NSA2P6, RN7SL767P, and RN7SL473P) were obtained, and a preliminary prediction model was established, in which ZNF556 was a risk factor, and the rest were protective factors. Single GSEA showed that pathways such as systemic lupus erythematosus might play an important role in the initial lymphatic metastasis of COAD. GO and KEGG enrichment analysis of 1727 genes supported this result. Immune infiltration analysis showed that six genes were significantly correlated with T cell and NK cell families. CONCLUSION: Six core genes may affect COAD initial lymphatic metastasis through the systemic lupus erythematosus pathway and immune cell infiltration. Hindawi 2022-08-29 /pmc/articles/PMC9444393/ /pubmed/36072412 http://dx.doi.org/10.1155/2022/4304361 Text en Copyright © 2022 Baoquan Wang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Baoquan
Yin, Changjun
Yang, Xu
Shi, Huibo
Zhang, Zheng
Zhou, Jun
Zhang, Peitong
Six Genes Associated with Lymphatic Metastasis in Colon Adenocarcinoma Linked to Prognostic Value and Tumor Immune Cell Infiltration
title Six Genes Associated with Lymphatic Metastasis in Colon Adenocarcinoma Linked to Prognostic Value and Tumor Immune Cell Infiltration
title_full Six Genes Associated with Lymphatic Metastasis in Colon Adenocarcinoma Linked to Prognostic Value and Tumor Immune Cell Infiltration
title_fullStr Six Genes Associated with Lymphatic Metastasis in Colon Adenocarcinoma Linked to Prognostic Value and Tumor Immune Cell Infiltration
title_full_unstemmed Six Genes Associated with Lymphatic Metastasis in Colon Adenocarcinoma Linked to Prognostic Value and Tumor Immune Cell Infiltration
title_short Six Genes Associated with Lymphatic Metastasis in Colon Adenocarcinoma Linked to Prognostic Value and Tumor Immune Cell Infiltration
title_sort six genes associated with lymphatic metastasis in colon adenocarcinoma linked to prognostic value and tumor immune cell infiltration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444393/
https://www.ncbi.nlm.nih.gov/pubmed/36072412
http://dx.doi.org/10.1155/2022/4304361
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