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Comprehensive analysis reveals the value of the expression of chromobox family members for bladder urothelial carcinoma prognosis
Bladder urothelial carcinoma (BLCA) accounts for 95% of all cases of bladder cancer worldwide, with a high incidence and poor prognosis. Chromobox (CBX) proteins play a key role in numerous malignant tumors; however, the role of CBX in BLCA remains unknown. Herein, the present study found that, comp...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031291/ https://www.ncbi.nlm.nih.gov/pubmed/36970607 http://dx.doi.org/10.3892/ol.2023.13758 |
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author | Meng, Xuan Cao, Runfu Liu, Xiaoqiang Fu, Bin Luo, Lianmin Jiang, Meichun Wang, Kaihong Liu, Yifu Zhu, Qiqi Yang, Chao Zhou, Libo |
author_facet | Meng, Xuan Cao, Runfu Liu, Xiaoqiang Fu, Bin Luo, Lianmin Jiang, Meichun Wang, Kaihong Liu, Yifu Zhu, Qiqi Yang, Chao Zhou, Libo |
author_sort | Meng, Xuan |
collection | PubMed |
description | Bladder urothelial carcinoma (BLCA) accounts for 95% of all cases of bladder cancer worldwide, with a high incidence and poor prognosis. Chromobox (CBX) proteins play a key role in numerous malignant tumors; however, the role of CBX in BLCA remains unknown. Herein, the present study found that, compared with in normal bladder tissues, the expression levels of CBX1, CBX2, CBX3, CBX4 and CBX8 were markedly increased in BLCA tissues, as determined by Tumor Immune Estimation Resource, UALCAN and ONCOMINE analyses, whereas CBX6 and CBX7 were decreased in BLCA tissues. Furthermore, evident hypomethylation in the promoters of CBX1, and CBX2, as well as significant hypermethylation in the promoters of CBX5, CBX6 and CBX7, was detected in BLCA tissues compared with in normal bladder tissues. The expression of CBX1, CBX2 and CBX7 was involved in the prognosis of patients with BLCA. Low CBX7 expression was strongly associated with poorer overall survival in patients with BLCA, whereas high CBX1 and CBX2 expression was associated with poorer progression-free survival. Besides, significant associations were determined between the expression of CBXs and immune cell infiltration, including dendritic cells, neutrophils, macrophages, CD4(+) T cells, CD8(+) T cells and B cells. Overall, the current results may provide a rationale for developing new targets and prognostic markers for BLCA therapy. |
format | Online Article Text |
id | pubmed-10031291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-100312912023-03-23 Comprehensive analysis reveals the value of the expression of chromobox family members for bladder urothelial carcinoma prognosis Meng, Xuan Cao, Runfu Liu, Xiaoqiang Fu, Bin Luo, Lianmin Jiang, Meichun Wang, Kaihong Liu, Yifu Zhu, Qiqi Yang, Chao Zhou, Libo Oncol Lett Articles Bladder urothelial carcinoma (BLCA) accounts for 95% of all cases of bladder cancer worldwide, with a high incidence and poor prognosis. Chromobox (CBX) proteins play a key role in numerous malignant tumors; however, the role of CBX in BLCA remains unknown. Herein, the present study found that, compared with in normal bladder tissues, the expression levels of CBX1, CBX2, CBX3, CBX4 and CBX8 were markedly increased in BLCA tissues, as determined by Tumor Immune Estimation Resource, UALCAN and ONCOMINE analyses, whereas CBX6 and CBX7 were decreased in BLCA tissues. Furthermore, evident hypomethylation in the promoters of CBX1, and CBX2, as well as significant hypermethylation in the promoters of CBX5, CBX6 and CBX7, was detected in BLCA tissues compared with in normal bladder tissues. The expression of CBX1, CBX2 and CBX7 was involved in the prognosis of patients with BLCA. Low CBX7 expression was strongly associated with poorer overall survival in patients with BLCA, whereas high CBX1 and CBX2 expression was associated with poorer progression-free survival. Besides, significant associations were determined between the expression of CBXs and immune cell infiltration, including dendritic cells, neutrophils, macrophages, CD4(+) T cells, CD8(+) T cells and B cells. Overall, the current results may provide a rationale for developing new targets and prognostic markers for BLCA therapy. D.A. Spandidos 2023-03-14 /pmc/articles/PMC10031291/ /pubmed/36970607 http://dx.doi.org/10.3892/ol.2023.13758 Text en Copyright: © Meng 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 Meng, Xuan Cao, Runfu Liu, Xiaoqiang Fu, Bin Luo, Lianmin Jiang, Meichun Wang, Kaihong Liu, Yifu Zhu, Qiqi Yang, Chao Zhou, Libo Comprehensive analysis reveals the value of the expression of chromobox family members for bladder urothelial carcinoma prognosis |
title | Comprehensive analysis reveals the value of the expression of chromobox family members for bladder urothelial carcinoma prognosis |
title_full | Comprehensive analysis reveals the value of the expression of chromobox family members for bladder urothelial carcinoma prognosis |
title_fullStr | Comprehensive analysis reveals the value of the expression of chromobox family members for bladder urothelial carcinoma prognosis |
title_full_unstemmed | Comprehensive analysis reveals the value of the expression of chromobox family members for bladder urothelial carcinoma prognosis |
title_short | Comprehensive analysis reveals the value of the expression of chromobox family members for bladder urothelial carcinoma prognosis |
title_sort | comprehensive analysis reveals the value of the expression of chromobox family members for bladder urothelial carcinoma prognosis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031291/ https://www.ncbi.nlm.nih.gov/pubmed/36970607 http://dx.doi.org/10.3892/ol.2023.13758 |
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