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Aquaporin 1 suppresses apoptosis and affects prognosis in esophageal squamous cell carcinoma

Aquaporin 1 (AQP1) is a membrane protein whose main function is to transfer water across cellular membranes. Recent studies have described important roles for AQP1 in epithelial carcinogenesis and tumor behavior. The objectives of the present study were to investigate the role of AQP1 in the regulat...

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Autores principales: Yamazato, Yuzo, Shiozaki, Atsushi, Ichikawa, Daisuke, Kosuga, Toshiyuki, Shoda, Katsutoshi, Arita, Tomohiro, Konishi, Hirotaka, Komatsu, Shuhei, Kubota, Takeshi, Fujiwara, Hitoshi, Okamoto, Kazuma, Kishimoto, Mitsuo, Konishi, Eiichi, Marunaka, Yoshinori, Otsuji, Eigo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057448/
https://www.ncbi.nlm.nih.gov/pubmed/30042826
http://dx.doi.org/10.18632/oncotarget.25722
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author Yamazato, Yuzo
Shiozaki, Atsushi
Ichikawa, Daisuke
Kosuga, Toshiyuki
Shoda, Katsutoshi
Arita, Tomohiro
Konishi, Hirotaka
Komatsu, Shuhei
Kubota, Takeshi
Fujiwara, Hitoshi
Okamoto, Kazuma
Kishimoto, Mitsuo
Konishi, Eiichi
Marunaka, Yoshinori
Otsuji, Eigo
author_facet Yamazato, Yuzo
Shiozaki, Atsushi
Ichikawa, Daisuke
Kosuga, Toshiyuki
Shoda, Katsutoshi
Arita, Tomohiro
Konishi, Hirotaka
Komatsu, Shuhei
Kubota, Takeshi
Fujiwara, Hitoshi
Okamoto, Kazuma
Kishimoto, Mitsuo
Konishi, Eiichi
Marunaka, Yoshinori
Otsuji, Eigo
author_sort Yamazato, Yuzo
collection PubMed
description Aquaporin 1 (AQP1) is a membrane protein whose main function is to transfer water across cellular membranes. Recent studies have described important roles for AQP1 in epithelial carcinogenesis and tumor behavior. The objectives of the present study were to investigate the role of AQP1 in the regulation of genes involved in tumor progression and the clinicopathological significance of its expression in esophageal squamous cell carcinoma (ESCC). An immunohistochemical analysis was performed on 50 primary tumor samples underwent esophagectomy. AQP1 was primarily located in the cytoplasm and/or the nuclear membrane of carcinoma cells. The 5-year survival rate of patients with the “cytoplasm dominant” expression of AQP1 (47.1%) was significantly lower than other patients (83.2%). The depletion of AQP1 using siRNA induced apoptosis in TE5 and TE15 cells. The results of microarray analysis revealed that Death receptor signaling pathway-related genes were changed in AQP1-depleted TE5 cells. In conclusion, the results of the present study suggested that the cytoplasm dominant expression of AQP1 is related to a poor prognosis in patients with ESCC, and that it activates tumor progression by affecting Death receptor signaling pathway. These results provide insights into the role of AQP1 as a mediator of and/or a biomarker for ESCC.
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spelling pubmed-60574482018-07-24 Aquaporin 1 suppresses apoptosis and affects prognosis in esophageal squamous cell carcinoma Yamazato, Yuzo Shiozaki, Atsushi Ichikawa, Daisuke Kosuga, Toshiyuki Shoda, Katsutoshi Arita, Tomohiro Konishi, Hirotaka Komatsu, Shuhei Kubota, Takeshi Fujiwara, Hitoshi Okamoto, Kazuma Kishimoto, Mitsuo Konishi, Eiichi Marunaka, Yoshinori Otsuji, Eigo Oncotarget Research Paper Aquaporin 1 (AQP1) is a membrane protein whose main function is to transfer water across cellular membranes. Recent studies have described important roles for AQP1 in epithelial carcinogenesis and tumor behavior. The objectives of the present study were to investigate the role of AQP1 in the regulation of genes involved in tumor progression and the clinicopathological significance of its expression in esophageal squamous cell carcinoma (ESCC). An immunohistochemical analysis was performed on 50 primary tumor samples underwent esophagectomy. AQP1 was primarily located in the cytoplasm and/or the nuclear membrane of carcinoma cells. The 5-year survival rate of patients with the “cytoplasm dominant” expression of AQP1 (47.1%) was significantly lower than other patients (83.2%). The depletion of AQP1 using siRNA induced apoptosis in TE5 and TE15 cells. The results of microarray analysis revealed that Death receptor signaling pathway-related genes were changed in AQP1-depleted TE5 cells. In conclusion, the results of the present study suggested that the cytoplasm dominant expression of AQP1 is related to a poor prognosis in patients with ESCC, and that it activates tumor progression by affecting Death receptor signaling pathway. These results provide insights into the role of AQP1 as a mediator of and/or a biomarker for ESCC. Impact Journals LLC 2018-07-06 /pmc/articles/PMC6057448/ /pubmed/30042826 http://dx.doi.org/10.18632/oncotarget.25722 Text en Copyright: © 2018 Yamazato et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Yamazato, Yuzo
Shiozaki, Atsushi
Ichikawa, Daisuke
Kosuga, Toshiyuki
Shoda, Katsutoshi
Arita, Tomohiro
Konishi, Hirotaka
Komatsu, Shuhei
Kubota, Takeshi
Fujiwara, Hitoshi
Okamoto, Kazuma
Kishimoto, Mitsuo
Konishi, Eiichi
Marunaka, Yoshinori
Otsuji, Eigo
Aquaporin 1 suppresses apoptosis and affects prognosis in esophageal squamous cell carcinoma
title Aquaporin 1 suppresses apoptosis and affects prognosis in esophageal squamous cell carcinoma
title_full Aquaporin 1 suppresses apoptosis and affects prognosis in esophageal squamous cell carcinoma
title_fullStr Aquaporin 1 suppresses apoptosis and affects prognosis in esophageal squamous cell carcinoma
title_full_unstemmed Aquaporin 1 suppresses apoptosis and affects prognosis in esophageal squamous cell carcinoma
title_short Aquaporin 1 suppresses apoptosis and affects prognosis in esophageal squamous cell carcinoma
title_sort aquaporin 1 suppresses apoptosis and affects prognosis in esophageal squamous cell carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057448/
https://www.ncbi.nlm.nih.gov/pubmed/30042826
http://dx.doi.org/10.18632/oncotarget.25722
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