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Upregulated Expression of Cancer-Derived Immunoglobulin G Is Associated With Progression in Glioma
OBJECTIVE: Gliomas are the most aggressive intracranial tumors accounting for the vast majority of brain tumors with very poor prognosis and overall survival (OS). Cancer-derived immunoglobulin G (cancer-IgG) has been found to be widely expressed in several malignancies such as breast cancer, colore...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8574069/ https://www.ncbi.nlm.nih.gov/pubmed/34760705 http://dx.doi.org/10.3389/fonc.2021.758856 |
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author | Wang, Guohui Li, Haonan Pan, Jie Yan, Tianfang Zhou, Huandi Han, Xuetao Su, Linlin Hou, Liubing Xue, Xiaoying |
author_facet | Wang, Guohui Li, Haonan Pan, Jie Yan, Tianfang Zhou, Huandi Han, Xuetao Su, Linlin Hou, Liubing Xue, Xiaoying |
author_sort | Wang, Guohui |
collection | PubMed |
description | OBJECTIVE: Gliomas are the most aggressive intracranial tumors accounting for the vast majority of brain tumors with very poor prognosis and overall survival (OS). Cancer-derived immunoglobulin G (cancer-IgG) has been found to be widely expressed in several malignancies such as breast cancer, colorectal cancer, and lung cancer. Cancer-IgG could promote tumorigenesis and progression. However, its role in glioma has not been revealed yet. METHODS: We mined open databases including the Chinese Glioma Genome Atlas (CGGA), The Cancer Genome Atlas (TCGA), and the Gene Expression Omnibus (GEO) to study the role of IGHG1, which encodes cancer-IgG in glioma. Examination of the differential expression of IGHG1 was carried out in the GEO and TCGA databases. Furthermore, its expression in different molecular subtypes was analyzed. Stratified analysis was performed with clinical features. Subsequently, immune infiltration analysis was conducted using single-sample gene set enrichment analysis (ssGSEA). GSEA was performed to reveal the mechanisms of IGHG1. Lastly, immunohistochemistry was processed to validate our findings. RESULTS: In this study, we found that the expression of IGHG1 was higher in glioma and molecular subtypes with poor prognosis. The overall survival of patients with a high expression of IGHG1 was worse in the stratified analysis. Immune infiltration analysis indicated that the expression level of IGHG1 was positively correlated with the stromal score, ESTIMATE score, and immune score and negatively correlated with tumor purity. Results from the GSEA and DAVID demonstrated that IGHG1 may function in phagosome, antigen processing and presentation, extracellular matrix structural constituent, antigen binding, and collagen-containing extracellular matrix. Finally, immunohistochemistry assay validated our findings that patients with a high expression of cancer-IgG had poor OS and disease-free survival (DFS). CONCLUSION: Cancer-IgG is a promising biomarker of diagnosis and treatment for patients with glioma. |
format | Online Article Text |
id | pubmed-8574069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85740692021-11-09 Upregulated Expression of Cancer-Derived Immunoglobulin G Is Associated With Progression in Glioma Wang, Guohui Li, Haonan Pan, Jie Yan, Tianfang Zhou, Huandi Han, Xuetao Su, Linlin Hou, Liubing Xue, Xiaoying Front Oncol Oncology OBJECTIVE: Gliomas are the most aggressive intracranial tumors accounting for the vast majority of brain tumors with very poor prognosis and overall survival (OS). Cancer-derived immunoglobulin G (cancer-IgG) has been found to be widely expressed in several malignancies such as breast cancer, colorectal cancer, and lung cancer. Cancer-IgG could promote tumorigenesis and progression. However, its role in glioma has not been revealed yet. METHODS: We mined open databases including the Chinese Glioma Genome Atlas (CGGA), The Cancer Genome Atlas (TCGA), and the Gene Expression Omnibus (GEO) to study the role of IGHG1, which encodes cancer-IgG in glioma. Examination of the differential expression of IGHG1 was carried out in the GEO and TCGA databases. Furthermore, its expression in different molecular subtypes was analyzed. Stratified analysis was performed with clinical features. Subsequently, immune infiltration analysis was conducted using single-sample gene set enrichment analysis (ssGSEA). GSEA was performed to reveal the mechanisms of IGHG1. Lastly, immunohistochemistry was processed to validate our findings. RESULTS: In this study, we found that the expression of IGHG1 was higher in glioma and molecular subtypes with poor prognosis. The overall survival of patients with a high expression of IGHG1 was worse in the stratified analysis. Immune infiltration analysis indicated that the expression level of IGHG1 was positively correlated with the stromal score, ESTIMATE score, and immune score and negatively correlated with tumor purity. Results from the GSEA and DAVID demonstrated that IGHG1 may function in phagosome, antigen processing and presentation, extracellular matrix structural constituent, antigen binding, and collagen-containing extracellular matrix. Finally, immunohistochemistry assay validated our findings that patients with a high expression of cancer-IgG had poor OS and disease-free survival (DFS). CONCLUSION: Cancer-IgG is a promising biomarker of diagnosis and treatment for patients with glioma. Frontiers Media S.A. 2021-10-25 /pmc/articles/PMC8574069/ /pubmed/34760705 http://dx.doi.org/10.3389/fonc.2021.758856 Text en Copyright © 2021 Wang, Li, Pan, Yan, Zhou, Han, Su, Hou and Xue 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 | Oncology Wang, Guohui Li, Haonan Pan, Jie Yan, Tianfang Zhou, Huandi Han, Xuetao Su, Linlin Hou, Liubing Xue, Xiaoying Upregulated Expression of Cancer-Derived Immunoglobulin G Is Associated With Progression in Glioma |
title | Upregulated Expression of Cancer-Derived Immunoglobulin G Is Associated With Progression in Glioma |
title_full | Upregulated Expression of Cancer-Derived Immunoglobulin G Is Associated With Progression in Glioma |
title_fullStr | Upregulated Expression of Cancer-Derived Immunoglobulin G Is Associated With Progression in Glioma |
title_full_unstemmed | Upregulated Expression of Cancer-Derived Immunoglobulin G Is Associated With Progression in Glioma |
title_short | Upregulated Expression of Cancer-Derived Immunoglobulin G Is Associated With Progression in Glioma |
title_sort | upregulated expression of cancer-derived immunoglobulin g is associated with progression in glioma |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8574069/ https://www.ncbi.nlm.nih.gov/pubmed/34760705 http://dx.doi.org/10.3389/fonc.2021.758856 |
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