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TSPAN4 is a prognostic and immune target in Glioblastoma multiforme
Background: Atherosclerosis can impact cancer progression due to the cholesterol and calcium metabolism, illustrating the links between atherosclerosis and cancer metastasis. Tetraspanin 4 (TSPAN4) may help understand migrasomes in diseases and provide novel targets for treatment. Methods: TSPAN4 ex...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9853066/ https://www.ncbi.nlm.nih.gov/pubmed/36685274 http://dx.doi.org/10.3389/fmolb.2022.1030057 |
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author | Zheng, Yue Lang, Yuheng Qi, Bingcai Wang, Yuchao Gao, Wenqing Li, Tong |
author_facet | Zheng, Yue Lang, Yuheng Qi, Bingcai Wang, Yuchao Gao, Wenqing Li, Tong |
author_sort | Zheng, Yue |
collection | PubMed |
description | Background: Atherosclerosis can impact cancer progression due to the cholesterol and calcium metabolism, illustrating the links between atherosclerosis and cancer metastasis. Tetraspanin 4 (TSPAN4) may help understand migrasomes in diseases and provide novel targets for treatment. Methods: TSPAN4 expression in atherosclerosis Gene Expression Omnibus (EO) dataset and multiple omics data were explored, such as enriched pathways analysis, protein-protein interaction analysis, immune subtypes as well as diagnostic and prognostic value in pan-cancer. The relationship between Glioblastoma multiforme (GBM) and TSPAN4 was further investigated. Results: Compared to control, TSPAN4 expression was upregulated in foam cells from patients with atherosclerosis and survival analysis demonstrated high TSPAN4 expression contributes to poor prognosis. TSPAN4 expression differs significantly in immune subtypes of cancers, which can be a diagnostic and prognostic target of cancers due to the high accuracy. Overall survival analysis of subgroups demonstrated that higher TSPAN4 expression had a worse prognosis and the univariate analysis and multivariate analysis demonstrated age, TSPAN4 expression, WHO grade, IDH status and histological types were independent risk factors of Glioblastoma multiforme. Conclusion: The TSPAN4 expression was associated with atherosclerosis progression and pan-cancer, especially in Glioblastoma multiforme and GBMLGG. Therefore, TSPAN4 may serve as a potential biomarker and the crosstalk between atherosclerosis and tumor progression. The results are not fully validated and further studies are still needed to validate in vivo and in vitro. |
format | Online Article Text |
id | pubmed-9853066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98530662023-01-21 TSPAN4 is a prognostic and immune target in Glioblastoma multiforme Zheng, Yue Lang, Yuheng Qi, Bingcai Wang, Yuchao Gao, Wenqing Li, Tong Front Mol Biosci Molecular Biosciences Background: Atherosclerosis can impact cancer progression due to the cholesterol and calcium metabolism, illustrating the links between atherosclerosis and cancer metastasis. Tetraspanin 4 (TSPAN4) may help understand migrasomes in diseases and provide novel targets for treatment. Methods: TSPAN4 expression in atherosclerosis Gene Expression Omnibus (EO) dataset and multiple omics data were explored, such as enriched pathways analysis, protein-protein interaction analysis, immune subtypes as well as diagnostic and prognostic value in pan-cancer. The relationship between Glioblastoma multiforme (GBM) and TSPAN4 was further investigated. Results: Compared to control, TSPAN4 expression was upregulated in foam cells from patients with atherosclerosis and survival analysis demonstrated high TSPAN4 expression contributes to poor prognosis. TSPAN4 expression differs significantly in immune subtypes of cancers, which can be a diagnostic and prognostic target of cancers due to the high accuracy. Overall survival analysis of subgroups demonstrated that higher TSPAN4 expression had a worse prognosis and the univariate analysis and multivariate analysis demonstrated age, TSPAN4 expression, WHO grade, IDH status and histological types were independent risk factors of Glioblastoma multiforme. Conclusion: The TSPAN4 expression was associated with atherosclerosis progression and pan-cancer, especially in Glioblastoma multiforme and GBMLGG. Therefore, TSPAN4 may serve as a potential biomarker and the crosstalk between atherosclerosis and tumor progression. The results are not fully validated and further studies are still needed to validate in vivo and in vitro. Frontiers Media S.A. 2023-01-06 /pmc/articles/PMC9853066/ /pubmed/36685274 http://dx.doi.org/10.3389/fmolb.2022.1030057 Text en Copyright © 2023 Zheng, Lang, Qi, Wang, Gao and Li. 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 | Molecular Biosciences Zheng, Yue Lang, Yuheng Qi, Bingcai Wang, Yuchao Gao, Wenqing Li, Tong TSPAN4 is a prognostic and immune target in Glioblastoma multiforme |
title | TSPAN4 is a prognostic and immune target in Glioblastoma multiforme |
title_full | TSPAN4 is a prognostic and immune target in Glioblastoma multiforme |
title_fullStr | TSPAN4 is a prognostic and immune target in Glioblastoma multiforme |
title_full_unstemmed | TSPAN4 is a prognostic and immune target in Glioblastoma multiforme |
title_short | TSPAN4 is a prognostic and immune target in Glioblastoma multiforme |
title_sort | tspan4 is a prognostic and immune target in glioblastoma multiforme |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9853066/ https://www.ncbi.nlm.nih.gov/pubmed/36685274 http://dx.doi.org/10.3389/fmolb.2022.1030057 |
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