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TPX2 expression is associated with poor survival in gastric cancer
BACKGROUND: Targeting protein for Xenopus kinesin-like protein 2 (TPX2) is a microtubule-associated protein required for microtubule formation in human cells. Several studies have demonstrated that TPX2 is overexpressed in multiple tumor types and promotes tumor growth and metastasis. However, there...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223319/ https://www.ncbi.nlm.nih.gov/pubmed/28069036 http://dx.doi.org/10.1186/s12957-016-1095-y |
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author | Tomii, Chiharu Inokuchi, Mikito Takagi, Yoko Ishikawa, Toshiaki Otsuki, Sho Uetake, Hiroyuki Kojima, Kazuyuki Kawano, Tatsuyuki |
author_facet | Tomii, Chiharu Inokuchi, Mikito Takagi, Yoko Ishikawa, Toshiaki Otsuki, Sho Uetake, Hiroyuki Kojima, Kazuyuki Kawano, Tatsuyuki |
author_sort | Tomii, Chiharu |
collection | PubMed |
description | BACKGROUND: Targeting protein for Xenopus kinesin-like protein 2 (TPX2) is a microtubule-associated protein required for microtubule formation in human cells. Several studies have demonstrated that TPX2 is overexpressed in multiple tumor types and promotes tumor growth and metastasis. However, there have been few reports regarding its role in gastric cancer. In this study, we evaluated TPX2 expression and investigated its correlations with gastric cancer clinicopathological features and prognosis. METHODS: Tumor samples were obtained from 290 patients with gastric adenocarcinoma who had undergone gastrectomy. The expression of TPX2 protein was examined using immunohistochemical staining. TPX2 messenger RNA (mRNA) levels were evaluated using real-time quantitative reverse transcription PCR in 19 of the gastric cancer tumors and adjacent normal tissues. RESULTS: The mRNA levels of TPX2 were significantly higher in gastric cancer tissues than in matched adjacent normal tissues (p = 0.004). In the immunohistochemical analysis, TPX2 overexpression was found in 123 (42.4%) of 290 patients. High TPX2 expression was positively associated with age, type of histology, depth of tumor, lymph node metastasis, stage, and remote metastasis or recurrence. High TPX2 expression was significantly associated with poorer disease-specific survival (p = 0.004) and relapse-free interval (p = 0.013). CONCLUSIONS: Our results indicated that high TPX2 expression was associated with tumor progression and poor survival in gastric cancer. |
format | Online Article Text |
id | pubmed-5223319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52233192017-01-11 TPX2 expression is associated with poor survival in gastric cancer Tomii, Chiharu Inokuchi, Mikito Takagi, Yoko Ishikawa, Toshiaki Otsuki, Sho Uetake, Hiroyuki Kojima, Kazuyuki Kawano, Tatsuyuki World J Surg Oncol Research BACKGROUND: Targeting protein for Xenopus kinesin-like protein 2 (TPX2) is a microtubule-associated protein required for microtubule formation in human cells. Several studies have demonstrated that TPX2 is overexpressed in multiple tumor types and promotes tumor growth and metastasis. However, there have been few reports regarding its role in gastric cancer. In this study, we evaluated TPX2 expression and investigated its correlations with gastric cancer clinicopathological features and prognosis. METHODS: Tumor samples were obtained from 290 patients with gastric adenocarcinoma who had undergone gastrectomy. The expression of TPX2 protein was examined using immunohistochemical staining. TPX2 messenger RNA (mRNA) levels were evaluated using real-time quantitative reverse transcription PCR in 19 of the gastric cancer tumors and adjacent normal tissues. RESULTS: The mRNA levels of TPX2 were significantly higher in gastric cancer tissues than in matched adjacent normal tissues (p = 0.004). In the immunohistochemical analysis, TPX2 overexpression was found in 123 (42.4%) of 290 patients. High TPX2 expression was positively associated with age, type of histology, depth of tumor, lymph node metastasis, stage, and remote metastasis or recurrence. High TPX2 expression was significantly associated with poorer disease-specific survival (p = 0.004) and relapse-free interval (p = 0.013). CONCLUSIONS: Our results indicated that high TPX2 expression was associated with tumor progression and poor survival in gastric cancer. BioMed Central 2017-01-09 /pmc/articles/PMC5223319/ /pubmed/28069036 http://dx.doi.org/10.1186/s12957-016-1095-y Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Tomii, Chiharu Inokuchi, Mikito Takagi, Yoko Ishikawa, Toshiaki Otsuki, Sho Uetake, Hiroyuki Kojima, Kazuyuki Kawano, Tatsuyuki TPX2 expression is associated with poor survival in gastric cancer |
title | TPX2 expression is associated with poor survival in gastric cancer |
title_full | TPX2 expression is associated with poor survival in gastric cancer |
title_fullStr | TPX2 expression is associated with poor survival in gastric cancer |
title_full_unstemmed | TPX2 expression is associated with poor survival in gastric cancer |
title_short | TPX2 expression is associated with poor survival in gastric cancer |
title_sort | tpx2 expression is associated with poor survival in gastric cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223319/ https://www.ncbi.nlm.nih.gov/pubmed/28069036 http://dx.doi.org/10.1186/s12957-016-1095-y |
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