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Steroid sulfatase promotes invasion through epithelial-mesenchymal transition and predicts the progression of bladder cancer
Androgen signal has been recently suggested to be associated with the progression of bladder cancer. Steroid sulfatase (STS) is a steroid sulfate activation enzyme, considered to be one of the key enzymes in the androgen signaling pathway. However, the role of STS in bladder cancer has not been eluc...
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/PMC6257456/ https://www.ncbi.nlm.nih.gov/pubmed/30542396 http://dx.doi.org/10.3892/etm.2018.6787 |
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author | Shimizu, Yasuomi Tamada, Satoshi Kato, Minoru Takeyama, Yuji Fujioka, Masaki Kakehashi, Anna Nakatani, Tatsuya Wanibuchi, Hideki Gi, Min |
author_facet | Shimizu, Yasuomi Tamada, Satoshi Kato, Minoru Takeyama, Yuji Fujioka, Masaki Kakehashi, Anna Nakatani, Tatsuya Wanibuchi, Hideki Gi, Min |
author_sort | Shimizu, Yasuomi |
collection | PubMed |
description | Androgen signal has been recently suggested to be associated with the progression of bladder cancer. Steroid sulfatase (STS) is a steroid sulfate activation enzyme, considered to be one of the key enzymes in the androgen signaling pathway. However, the role of STS in bladder cancer has not been elucidated. The purpose of the present study was to determine the clinical and functional significance of STS in bladder cancer. Immunohistochemical analysis of surgical specimens obtained by radical cystectomy (n=114) demonstrated that overexpression of STS was associated with the invasion of bladder cancer, as evidenced by the incidence of STS-positive cancers (11.5 and 37.1% in non-muscle invasive and muscle invasive bladder cancers, respectively; P=0.003). STS-positive cancer demonstrated shorter recurrence-free survival and cancer-specific survival (P=0.0027 and 0.0030, respectively). Furthermore, knockdown of STS significantly reduced cell migration and invasion capacities of bladder cancer cells (P<0.001 and P=0.005, respectively), accompanied by the upregulation of E-cadherin and downregulation of vimentin. In summary, the present study demonstrated that STS promotes the invasion capability of bladder cancer via regulation of the epithelial-mesenchymal transition, and may be a useful marker for predicting the progression of bladder cancers. |
format | Online Article Text |
id | pubmed-6257456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-62574562018-12-12 Steroid sulfatase promotes invasion through epithelial-mesenchymal transition and predicts the progression of bladder cancer Shimizu, Yasuomi Tamada, Satoshi Kato, Minoru Takeyama, Yuji Fujioka, Masaki Kakehashi, Anna Nakatani, Tatsuya Wanibuchi, Hideki Gi, Min Exp Ther Med Articles Androgen signal has been recently suggested to be associated with the progression of bladder cancer. Steroid sulfatase (STS) is a steroid sulfate activation enzyme, considered to be one of the key enzymes in the androgen signaling pathway. However, the role of STS in bladder cancer has not been elucidated. The purpose of the present study was to determine the clinical and functional significance of STS in bladder cancer. Immunohistochemical analysis of surgical specimens obtained by radical cystectomy (n=114) demonstrated that overexpression of STS was associated with the invasion of bladder cancer, as evidenced by the incidence of STS-positive cancers (11.5 and 37.1% in non-muscle invasive and muscle invasive bladder cancers, respectively; P=0.003). STS-positive cancer demonstrated shorter recurrence-free survival and cancer-specific survival (P=0.0027 and 0.0030, respectively). Furthermore, knockdown of STS significantly reduced cell migration and invasion capacities of bladder cancer cells (P<0.001 and P=0.005, respectively), accompanied by the upregulation of E-cadherin and downregulation of vimentin. In summary, the present study demonstrated that STS promotes the invasion capability of bladder cancer via regulation of the epithelial-mesenchymal transition, and may be a useful marker for predicting the progression of bladder cancers. D.A. Spandidos 2018-12 2018-09-21 /pmc/articles/PMC6257456/ /pubmed/30542396 http://dx.doi.org/10.3892/etm.2018.6787 Text en Copyright: © Shimizu 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 Shimizu, Yasuomi Tamada, Satoshi Kato, Minoru Takeyama, Yuji Fujioka, Masaki Kakehashi, Anna Nakatani, Tatsuya Wanibuchi, Hideki Gi, Min Steroid sulfatase promotes invasion through epithelial-mesenchymal transition and predicts the progression of bladder cancer |
title | Steroid sulfatase promotes invasion through epithelial-mesenchymal transition and predicts the progression of bladder cancer |
title_full | Steroid sulfatase promotes invasion through epithelial-mesenchymal transition and predicts the progression of bladder cancer |
title_fullStr | Steroid sulfatase promotes invasion through epithelial-mesenchymal transition and predicts the progression of bladder cancer |
title_full_unstemmed | Steroid sulfatase promotes invasion through epithelial-mesenchymal transition and predicts the progression of bladder cancer |
title_short | Steroid sulfatase promotes invasion through epithelial-mesenchymal transition and predicts the progression of bladder cancer |
title_sort | steroid sulfatase promotes invasion through epithelial-mesenchymal transition and predicts the progression of bladder cancer |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257456/ https://www.ncbi.nlm.nih.gov/pubmed/30542396 http://dx.doi.org/10.3892/etm.2018.6787 |
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