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Pan‑cancer analysis identified ARHGAP23 as a potential biomarker for pancreatic adenocarcinoma
Rho GTPASE-activating protein 23 (ARHGAP23) is known to activate RHO-GTPase and has an important role in the infiltration and metastasis of tumors. Although previous studies suggested its involvement in certain human cancers, its role in pan-cancer remains unclear. In the present study, the expressi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666083/ https://www.ncbi.nlm.nih.gov/pubmed/38022849 http://dx.doi.org/10.3892/mco.2023.2696 |
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author | Liu, Xiaolong Li, Xin Wang, Ling Yu, Kaihua Wu, Dean Tao, Pengxian Li, Yulan |
author_facet | Liu, Xiaolong Li, Xin Wang, Ling Yu, Kaihua Wu, Dean Tao, Pengxian Li, Yulan |
author_sort | Liu, Xiaolong |
collection | PubMed |
description | Rho GTPASE-activating protein 23 (ARHGAP23) is known to activate RHO-GTPase and has an important role in the infiltration and metastasis of tumors. Although previous studies suggested its involvement in certain human cancers, its role in pan-cancer remains unclear. In the present study, the expression, prognosis and potential functions of ARHGAP23 in pan-cancer were evaluated through various public databases such as Human Protein Atlas, Tumor IMmune Estimation Resource, Gene Set Co-Expression Analysis, Gene Expression Profiling Interactive Analysis, cBio Cancer Genomics Portal, Tumor-Immune System Interactions Database (TISIDB) and others. Through these data combined with a variety of biological information analysis methods, the potential role of ARHGAP23 as a carcinogenic gene was explored in the present study. The present analysis revealed that ARHGAP23 expressed abnormalities in >10 tumors, which was associated with differences in prognosis. Furthermore, the findings of the present study indicated that ARHGAP23 is associated with DNA methylation and multiple immune cell infiltrations in these tumors. ARHGAP23 expression was related to clinical prognosis, DNA methylation and immune infiltration. These findings support the potential of ARHGAP23 as a prognostic biomarker and a molecular target for cancer treatment. |
format | Online Article Text |
id | pubmed-10666083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-106660832023-11-03 Pan‑cancer analysis identified ARHGAP23 as a potential biomarker for pancreatic adenocarcinoma Liu, Xiaolong Li, Xin Wang, Ling Yu, Kaihua Wu, Dean Tao, Pengxian Li, Yulan Mol Clin Oncol Articles Rho GTPASE-activating protein 23 (ARHGAP23) is known to activate RHO-GTPase and has an important role in the infiltration and metastasis of tumors. Although previous studies suggested its involvement in certain human cancers, its role in pan-cancer remains unclear. In the present study, the expression, prognosis and potential functions of ARHGAP23 in pan-cancer were evaluated through various public databases such as Human Protein Atlas, Tumor IMmune Estimation Resource, Gene Set Co-Expression Analysis, Gene Expression Profiling Interactive Analysis, cBio Cancer Genomics Portal, Tumor-Immune System Interactions Database (TISIDB) and others. Through these data combined with a variety of biological information analysis methods, the potential role of ARHGAP23 as a carcinogenic gene was explored in the present study. The present analysis revealed that ARHGAP23 expressed abnormalities in >10 tumors, which was associated with differences in prognosis. Furthermore, the findings of the present study indicated that ARHGAP23 is associated with DNA methylation and multiple immune cell infiltrations in these tumors. ARHGAP23 expression was related to clinical prognosis, DNA methylation and immune infiltration. These findings support the potential of ARHGAP23 as a prognostic biomarker and a molecular target for cancer treatment. D.A. Spandidos 2023-11-03 /pmc/articles/PMC10666083/ /pubmed/38022849 http://dx.doi.org/10.3892/mco.2023.2696 Text en Copyright: © Liu et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Liu, Xiaolong Li, Xin Wang, Ling Yu, Kaihua Wu, Dean Tao, Pengxian Li, Yulan Pan‑cancer analysis identified ARHGAP23 as a potential biomarker for pancreatic adenocarcinoma |
title | Pan‑cancer analysis identified ARHGAP23 as a potential biomarker for pancreatic adenocarcinoma |
title_full | Pan‑cancer analysis identified ARHGAP23 as a potential biomarker for pancreatic adenocarcinoma |
title_fullStr | Pan‑cancer analysis identified ARHGAP23 as a potential biomarker for pancreatic adenocarcinoma |
title_full_unstemmed | Pan‑cancer analysis identified ARHGAP23 as a potential biomarker for pancreatic adenocarcinoma |
title_short | Pan‑cancer analysis identified ARHGAP23 as a potential biomarker for pancreatic adenocarcinoma |
title_sort | pan‑cancer analysis identified arhgap23 as a potential biomarker for pancreatic adenocarcinoma |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666083/ https://www.ncbi.nlm.nih.gov/pubmed/38022849 http://dx.doi.org/10.3892/mco.2023.2696 |
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