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Expression of S100A16 Is Associated with Biological Aggressiveness and Poor Prognosis in Patients with Bladder Cancer Who Underwent Radical Cystectomy
S100 calcium binding protein A16 (S100A16) is expressed in various cancers; however, there are few reports on S100A16 in bladder cancer (BC). We retrospectively investigated clinical data including clinicopathological features in 121 patients with BC who underwent radical cystectomy (RC). Immunohist...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10572706/ https://www.ncbi.nlm.nih.gov/pubmed/37833982 http://dx.doi.org/10.3390/ijms241914536 |
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author | Katsumata, Hiroki Matsumoto, Kazumasa Yanagita, Kengo Shimizu, Yuriko Hirano, Shuhei Kitajima, Kazuki Koguchi, Dai Ikeda, Masaomi Sato, Yuichi Iwamura, Masatsugu |
author_facet | Katsumata, Hiroki Matsumoto, Kazumasa Yanagita, Kengo Shimizu, Yuriko Hirano, Shuhei Kitajima, Kazuki Koguchi, Dai Ikeda, Masaomi Sato, Yuichi Iwamura, Masatsugu |
author_sort | Katsumata, Hiroki |
collection | PubMed |
description | S100 calcium binding protein A16 (S100A16) is expressed in various cancers; however, there are few reports on S100A16 in bladder cancer (BC). We retrospectively investigated clinical data including clinicopathological features in 121 patients with BC who underwent radical cystectomy (RC). Immunohistochemical staining was performed to evaluate S100A16 expression in archived specimens. Cases with >5% expression and more than moderate staining intensity on cancer cells were considered positive. S100A16 expression was observed in 54 patients (44.6%). Univariate analysis showed that S100A16 expression was significantly associated with age, pT stage, recurrence, and cancer-specific death. Kaplan–Meier analyses showed that patients with S100A16 expression had shorter overall survival (OS), cancer-specific survival (CSS), and recurrence-free survival (RFS) than those without S100A16 expression. In multivariate analysis, pT stage was an independent prognostic factor for OS and lymph node metastasis for CSS and RFS. S100A16 expression may be a biomarker of a biologically aggressive phenotype and poor prognosis in patients with BC who underwent RC. The PI3k/Akt signaling pathway is probably associated with S100A16 and may be a therapeutic target. |
format | Online Article Text |
id | pubmed-10572706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105727062023-10-14 Expression of S100A16 Is Associated with Biological Aggressiveness and Poor Prognosis in Patients with Bladder Cancer Who Underwent Radical Cystectomy Katsumata, Hiroki Matsumoto, Kazumasa Yanagita, Kengo Shimizu, Yuriko Hirano, Shuhei Kitajima, Kazuki Koguchi, Dai Ikeda, Masaomi Sato, Yuichi Iwamura, Masatsugu Int J Mol Sci Article S100 calcium binding protein A16 (S100A16) is expressed in various cancers; however, there are few reports on S100A16 in bladder cancer (BC). We retrospectively investigated clinical data including clinicopathological features in 121 patients with BC who underwent radical cystectomy (RC). Immunohistochemical staining was performed to evaluate S100A16 expression in archived specimens. Cases with >5% expression and more than moderate staining intensity on cancer cells were considered positive. S100A16 expression was observed in 54 patients (44.6%). Univariate analysis showed that S100A16 expression was significantly associated with age, pT stage, recurrence, and cancer-specific death. Kaplan–Meier analyses showed that patients with S100A16 expression had shorter overall survival (OS), cancer-specific survival (CSS), and recurrence-free survival (RFS) than those without S100A16 expression. In multivariate analysis, pT stage was an independent prognostic factor for OS and lymph node metastasis for CSS and RFS. S100A16 expression may be a biomarker of a biologically aggressive phenotype and poor prognosis in patients with BC who underwent RC. The PI3k/Akt signaling pathway is probably associated with S100A16 and may be a therapeutic target. MDPI 2023-09-26 /pmc/articles/PMC10572706/ /pubmed/37833982 http://dx.doi.org/10.3390/ijms241914536 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Katsumata, Hiroki Matsumoto, Kazumasa Yanagita, Kengo Shimizu, Yuriko Hirano, Shuhei Kitajima, Kazuki Koguchi, Dai Ikeda, Masaomi Sato, Yuichi Iwamura, Masatsugu Expression of S100A16 Is Associated with Biological Aggressiveness and Poor Prognosis in Patients with Bladder Cancer Who Underwent Radical Cystectomy |
title | Expression of S100A16 Is Associated with Biological Aggressiveness and Poor Prognosis in Patients with Bladder Cancer Who Underwent Radical Cystectomy |
title_full | Expression of S100A16 Is Associated with Biological Aggressiveness and Poor Prognosis in Patients with Bladder Cancer Who Underwent Radical Cystectomy |
title_fullStr | Expression of S100A16 Is Associated with Biological Aggressiveness and Poor Prognosis in Patients with Bladder Cancer Who Underwent Radical Cystectomy |
title_full_unstemmed | Expression of S100A16 Is Associated with Biological Aggressiveness and Poor Prognosis in Patients with Bladder Cancer Who Underwent Radical Cystectomy |
title_short | Expression of S100A16 Is Associated with Biological Aggressiveness and Poor Prognosis in Patients with Bladder Cancer Who Underwent Radical Cystectomy |
title_sort | expression of s100a16 is associated with biological aggressiveness and poor prognosis in patients with bladder cancer who underwent radical cystectomy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10572706/ https://www.ncbi.nlm.nih.gov/pubmed/37833982 http://dx.doi.org/10.3390/ijms241914536 |
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