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Muscarinic cholinergic signaling and overactive bladder-like symptoms associated with invasive bladder cancer
The objective of the present study was to explore the association between muscarinic cholinergic signaling and urothelial bladder tumors. Possible associations among overactive bladder (OAB) symptoms and bladder tumors were retrospectively investigated using a multicenter Chinese database with prosp...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019950/ https://www.ncbi.nlm.nih.gov/pubmed/29963145 http://dx.doi.org/10.3892/ol.2018.8715 |
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author | Wei, Wei Wang, Minggang Li, Yunglong Meng, Qinggui Tang, Yong Lu, Haoyuan Yu, Wenchao Cheng, Qiwei Li, You Xu, Long Jian, Shaojun Wu, Yuexian Yi, Xianlin Xie, Keji |
author_facet | Wei, Wei Wang, Minggang Li, Yunglong Meng, Qinggui Tang, Yong Lu, Haoyuan Yu, Wenchao Cheng, Qiwei Li, You Xu, Long Jian, Shaojun Wu, Yuexian Yi, Xianlin Xie, Keji |
author_sort | Wei, Wei |
collection | PubMed |
description | The objective of the present study was to explore the association between muscarinic cholinergic signaling and urothelial bladder tumors. Possible associations among overactive bladder (OAB) symptoms and bladder tumors were retrospectively investigated using a multicenter Chinese database with prospectively collected data since 2010. Firstly, it was demonstrated that OAB symptoms, such as urgency, were more severe in patients with invasive bladder cancer and were associated with a reduced prognosis. Following this, muscarinic cholinergic receptor 3 (M3R) expression in urothelium was determined to be lower in invasive cancer tissue than in adjacent non-cancerous tissue, yet M3R upregulation was associated with a reduced progression free survival (PFS) time. Additionally, it was also demonstrated that muscarinic cholinergic receptor 2 (M2R) was upregulated in the sub-urothelium, and this was also associated with a reduced PFS time. Furthermore, it was determined that cholinesterase and acetylcholinesterase were lower in invasive cancer than in non-invasive cancer. In conclusion, the results indicated that M3R expression was downregulated in invasive bladder cancer, which may have a role as a protective anti-oncogene, in contrast to its oncogenic role in numerous other cancer types. Therefore, muscarinic cholinergic signaling may be a novel therapeutic target for treating bladder cancer. |
format | Online Article Text |
id | pubmed-6019950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-60199502018-06-29 Muscarinic cholinergic signaling and overactive bladder-like symptoms associated with invasive bladder cancer Wei, Wei Wang, Minggang Li, Yunglong Meng, Qinggui Tang, Yong Lu, Haoyuan Yu, Wenchao Cheng, Qiwei Li, You Xu, Long Jian, Shaojun Wu, Yuexian Yi, Xianlin Xie, Keji Oncol Lett Articles The objective of the present study was to explore the association between muscarinic cholinergic signaling and urothelial bladder tumors. Possible associations among overactive bladder (OAB) symptoms and bladder tumors were retrospectively investigated using a multicenter Chinese database with prospectively collected data since 2010. Firstly, it was demonstrated that OAB symptoms, such as urgency, were more severe in patients with invasive bladder cancer and were associated with a reduced prognosis. Following this, muscarinic cholinergic receptor 3 (M3R) expression in urothelium was determined to be lower in invasive cancer tissue than in adjacent non-cancerous tissue, yet M3R upregulation was associated with a reduced progression free survival (PFS) time. Additionally, it was also demonstrated that muscarinic cholinergic receptor 2 (M2R) was upregulated in the sub-urothelium, and this was also associated with a reduced PFS time. Furthermore, it was determined that cholinesterase and acetylcholinesterase were lower in invasive cancer than in non-invasive cancer. In conclusion, the results indicated that M3R expression was downregulated in invasive bladder cancer, which may have a role as a protective anti-oncogene, in contrast to its oncogenic role in numerous other cancer types. Therefore, muscarinic cholinergic signaling may be a novel therapeutic target for treating bladder cancer. D.A. Spandidos 2018-07 2018-05-16 /pmc/articles/PMC6019950/ /pubmed/29963145 http://dx.doi.org/10.3892/ol.2018.8715 Text en Copyright: © Wei et al. 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 Wei, Wei Wang, Minggang Li, Yunglong Meng, Qinggui Tang, Yong Lu, Haoyuan Yu, Wenchao Cheng, Qiwei Li, You Xu, Long Jian, Shaojun Wu, Yuexian Yi, Xianlin Xie, Keji Muscarinic cholinergic signaling and overactive bladder-like symptoms associated with invasive bladder cancer |
title | Muscarinic cholinergic signaling and overactive bladder-like symptoms associated with invasive bladder cancer |
title_full | Muscarinic cholinergic signaling and overactive bladder-like symptoms associated with invasive bladder cancer |
title_fullStr | Muscarinic cholinergic signaling and overactive bladder-like symptoms associated with invasive bladder cancer |
title_full_unstemmed | Muscarinic cholinergic signaling and overactive bladder-like symptoms associated with invasive bladder cancer |
title_short | Muscarinic cholinergic signaling and overactive bladder-like symptoms associated with invasive bladder cancer |
title_sort | muscarinic cholinergic signaling and overactive bladder-like symptoms associated with invasive bladder cancer |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019950/ https://www.ncbi.nlm.nih.gov/pubmed/29963145 http://dx.doi.org/10.3892/ol.2018.8715 |
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