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Na(+)/H(+) exchanger 1 has tumor suppressive activity and prognostic value in esophageal squamous cell carcinoma
Na(+)/H(+) exchanger 1 (NHE1) is a plasma membrane transporter that controls intracellular pH and regulates apoptosis and invasion in various cancer cells. However, the function of NHE1 in esophageal squamous cell carcinoma (ESCC) cells and the relationship between the expression of NHE1 and prognos...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356793/ https://www.ncbi.nlm.nih.gov/pubmed/27902974 http://dx.doi.org/10.18632/oncotarget.13645 |
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author | Ariyoshi, Yosuke Shiozaki, Atsushi Ichikawa, Daisuke Shimizu, Hiroki Kosuga, Toshiyuki Konishi, Hirotaka Komatsu, Shuhei Fujiwara, Hitoshi Okamoto, Kazuma Kishimoto, Mitsuo Marunaka, Yoshinori Otsuji, Eigo |
author_facet | Ariyoshi, Yosuke Shiozaki, Atsushi Ichikawa, Daisuke Shimizu, Hiroki Kosuga, Toshiyuki Konishi, Hirotaka Komatsu, Shuhei Fujiwara, Hitoshi Okamoto, Kazuma Kishimoto, Mitsuo Marunaka, Yoshinori Otsuji, Eigo |
author_sort | Ariyoshi, Yosuke |
collection | PubMed |
description | Na(+)/H(+) exchanger 1 (NHE1) is a plasma membrane transporter that controls intracellular pH and regulates apoptosis and invasion in various cancer cells. However, the function of NHE1 in esophageal squamous cell carcinoma (ESCC) cells and the relationship between the expression of NHE1 and prognosis of ESCC remain unclear. We found that the knockdown of NHE1 in ESCC cells inhibited apoptosis and promoted cell proliferation, migration, and invasion and showed increases in Snail, β-catenin, and activation of PI3K-AKT signaling, which was consistent with the results obtained from microarrays. Microarrays results suggested that the knockdown of NHE1 suppressed Notch signaling pathway. An immunohistochemical investigation of 61 primary ESCC samples revealed that NHE1 was expressed at higher levels in well-differentiated tumors. The 5-year survival rate was poorer in the NHE1 low group (57.0%) than in the NHE1 high group (82.8%). Multivariate analyses revealed that the weak expression of NHE1 was associated with shorter postoperative survival (hazard ratio 3.570, 95% CI 1.291-11.484, p = 0.0135).We herein demonstrated that the suppression of NHE1 in ESCC may enhance malignant potential by mediating PI3K-AKT signaling and EMT via Notch signaling, and may be related to a poor prognosis in patients with ESCC. |
format | Online Article Text |
id | pubmed-5356793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53567932017-04-20 Na(+)/H(+) exchanger 1 has tumor suppressive activity and prognostic value in esophageal squamous cell carcinoma Ariyoshi, Yosuke Shiozaki, Atsushi Ichikawa, Daisuke Shimizu, Hiroki Kosuga, Toshiyuki Konishi, Hirotaka Komatsu, Shuhei Fujiwara, Hitoshi Okamoto, Kazuma Kishimoto, Mitsuo Marunaka, Yoshinori Otsuji, Eigo Oncotarget Research Paper Na(+)/H(+) exchanger 1 (NHE1) is a plasma membrane transporter that controls intracellular pH and regulates apoptosis and invasion in various cancer cells. However, the function of NHE1 in esophageal squamous cell carcinoma (ESCC) cells and the relationship between the expression of NHE1 and prognosis of ESCC remain unclear. We found that the knockdown of NHE1 in ESCC cells inhibited apoptosis and promoted cell proliferation, migration, and invasion and showed increases in Snail, β-catenin, and activation of PI3K-AKT signaling, which was consistent with the results obtained from microarrays. Microarrays results suggested that the knockdown of NHE1 suppressed Notch signaling pathway. An immunohistochemical investigation of 61 primary ESCC samples revealed that NHE1 was expressed at higher levels in well-differentiated tumors. The 5-year survival rate was poorer in the NHE1 low group (57.0%) than in the NHE1 high group (82.8%). Multivariate analyses revealed that the weak expression of NHE1 was associated with shorter postoperative survival (hazard ratio 3.570, 95% CI 1.291-11.484, p = 0.0135).We herein demonstrated that the suppression of NHE1 in ESCC may enhance malignant potential by mediating PI3K-AKT signaling and EMT via Notch signaling, and may be related to a poor prognosis in patients with ESCC. Impact Journals LLC 2016-11-26 /pmc/articles/PMC5356793/ /pubmed/27902974 http://dx.doi.org/10.18632/oncotarget.13645 Text en Copyright: © 2017 Ariyoshi et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Ariyoshi, Yosuke Shiozaki, Atsushi Ichikawa, Daisuke Shimizu, Hiroki Kosuga, Toshiyuki Konishi, Hirotaka Komatsu, Shuhei Fujiwara, Hitoshi Okamoto, Kazuma Kishimoto, Mitsuo Marunaka, Yoshinori Otsuji, Eigo Na(+)/H(+) exchanger 1 has tumor suppressive activity and prognostic value in esophageal squamous cell carcinoma |
title | Na(+)/H(+) exchanger 1 has tumor suppressive activity and prognostic value in esophageal squamous cell carcinoma |
title_full | Na(+)/H(+) exchanger 1 has tumor suppressive activity and prognostic value in esophageal squamous cell carcinoma |
title_fullStr | Na(+)/H(+) exchanger 1 has tumor suppressive activity and prognostic value in esophageal squamous cell carcinoma |
title_full_unstemmed | Na(+)/H(+) exchanger 1 has tumor suppressive activity and prognostic value in esophageal squamous cell carcinoma |
title_short | Na(+)/H(+) exchanger 1 has tumor suppressive activity and prognostic value in esophageal squamous cell carcinoma |
title_sort | na(+)/h(+) exchanger 1 has tumor suppressive activity and prognostic value in esophageal squamous cell carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356793/ https://www.ncbi.nlm.nih.gov/pubmed/27902974 http://dx.doi.org/10.18632/oncotarget.13645 |
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