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Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) association with lymph node metastasis predicts poor survival in oral squamous cell carcinoma patients

Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) is a multifunctional protein aberrantly expressed in various types of cancers. However, its expression pattern and clinical significance in oral squamous cell carcinoma (OSCC) remains unclear. In this study, we immunohistochemically investigate...

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Autores principales: Velmurugan, Bharath Kumar, Yeh, Kun-Tu, Lee, Chien-Hung, Lin, Shu-Hui, Chin, Mei-Chung, Chiang, Shang-Lun, Wang, Zhi-Hong, Hua, Chun-Hung, Tsai, Ming-Hsui, Chang, Jan-Gowth, Ko, Ying-Chin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905446/
https://www.ncbi.nlm.nih.gov/pubmed/26918356
http://dx.doi.org/10.18632/oncotarget.7681
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author Velmurugan, Bharath Kumar
Yeh, Kun-Tu
Lee, Chien-Hung
Lin, Shu-Hui
Chin, Mei-Chung
Chiang, Shang-Lun
Wang, Zhi-Hong
Hua, Chun-Hung
Tsai, Ming-Hsui
Chang, Jan-Gowth
Ko, Ying-Chin
author_facet Velmurugan, Bharath Kumar
Yeh, Kun-Tu
Lee, Chien-Hung
Lin, Shu-Hui
Chin, Mei-Chung
Chiang, Shang-Lun
Wang, Zhi-Hong
Hua, Chun-Hung
Tsai, Ming-Hsui
Chang, Jan-Gowth
Ko, Ying-Chin
author_sort Velmurugan, Bharath Kumar
collection PubMed
description Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) is a multifunctional protein aberrantly expressed in various types of cancers. However, its expression pattern and clinical significance in oral squamous cell carcinoma (OSCC) remains unclear. In this study, we immunohistochemically investigated the expression pattern of ANP32A in 259 OSCC patients and the results were correlated with clinicopathological factors using Allred, Klein and Immunoreactive scoring (IRS) system. Our data indicated that high expression of ANP32A was significantly associated with N stage and tumor differentiation status in OSCC patients. High ANP32A expression with N2/N3 stage had an increased mortality risk than low ANP32A expressing OSCC patients with N0/N1 stage. Functional studies revealed that knockdown of ANP32A significantly decreased the migration and invasion ability thereby concomitantly increasing E-cadherin and decreasing Slug, Claudin-1 and Vimentin expression in vitro. These results suggest that ANP32A is commonly increased in oral squamous cell carcinoma and ANP32A protein could act as a potential biomarker for prognosis assessment of oral cancer patients with lymph node metastasis.
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spelling pubmed-49054462016-06-24 Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) association with lymph node metastasis predicts poor survival in oral squamous cell carcinoma patients Velmurugan, Bharath Kumar Yeh, Kun-Tu Lee, Chien-Hung Lin, Shu-Hui Chin, Mei-Chung Chiang, Shang-Lun Wang, Zhi-Hong Hua, Chun-Hung Tsai, Ming-Hsui Chang, Jan-Gowth Ko, Ying-Chin Oncotarget Research Paper: Pathology Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) is a multifunctional protein aberrantly expressed in various types of cancers. However, its expression pattern and clinical significance in oral squamous cell carcinoma (OSCC) remains unclear. In this study, we immunohistochemically investigated the expression pattern of ANP32A in 259 OSCC patients and the results were correlated with clinicopathological factors using Allred, Klein and Immunoreactive scoring (IRS) system. Our data indicated that high expression of ANP32A was significantly associated with N stage and tumor differentiation status in OSCC patients. High ANP32A expression with N2/N3 stage had an increased mortality risk than low ANP32A expressing OSCC patients with N0/N1 stage. Functional studies revealed that knockdown of ANP32A significantly decreased the migration and invasion ability thereby concomitantly increasing E-cadherin and decreasing Slug, Claudin-1 and Vimentin expression in vitro. These results suggest that ANP32A is commonly increased in oral squamous cell carcinoma and ANP32A protein could act as a potential biomarker for prognosis assessment of oral cancer patients with lymph node metastasis. Impact Journals LLC 2016-02-24 /pmc/articles/PMC4905446/ /pubmed/26918356 http://dx.doi.org/10.18632/oncotarget.7681 Text en Copyright: © 2016 Velmurugan et al. http://creativecommons.org/licenses/by/2.5/ 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: Pathology
Velmurugan, Bharath Kumar
Yeh, Kun-Tu
Lee, Chien-Hung
Lin, Shu-Hui
Chin, Mei-Chung
Chiang, Shang-Lun
Wang, Zhi-Hong
Hua, Chun-Hung
Tsai, Ming-Hsui
Chang, Jan-Gowth
Ko, Ying-Chin
Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) association with lymph node metastasis predicts poor survival in oral squamous cell carcinoma patients
title Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) association with lymph node metastasis predicts poor survival in oral squamous cell carcinoma patients
title_full Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) association with lymph node metastasis predicts poor survival in oral squamous cell carcinoma patients
title_fullStr Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) association with lymph node metastasis predicts poor survival in oral squamous cell carcinoma patients
title_full_unstemmed Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) association with lymph node metastasis predicts poor survival in oral squamous cell carcinoma patients
title_short Acidic leucine-rich nuclear phosphoprotein-32A (ANP32A) association with lymph node metastasis predicts poor survival in oral squamous cell carcinoma patients
title_sort acidic leucine-rich nuclear phosphoprotein-32a (anp32a) association with lymph node metastasis predicts poor survival in oral squamous cell carcinoma patients
topic Research Paper: Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905446/
https://www.ncbi.nlm.nih.gov/pubmed/26918356
http://dx.doi.org/10.18632/oncotarget.7681
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