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CIP2A overexpression in Taiwanese oral cancer patients

Introduction: Oral cancer is a prevalent form of cancer worldwide, particularly in Taiwan, and mechanisms involved in oral squamous cell carcinoma (OSCC) progression remain relatively unknown. Cancerous inhibitor of protein phosphatase 2A (CIP2A), an oncoprotein, is aberrantly expressed in many huma...

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Autores principales: Velmurugan, Bharath Kumar, Wang, Hsin-Kai, Chung, Chia-Min, Lee, Chien-Hsun, Huang, Lan-Ru, Yeh, Kun-Tu, Lin, Shu-Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497856/
https://www.ncbi.nlm.nih.gov/pubmed/31114325
http://dx.doi.org/10.2147/CMAR.S201154
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author Velmurugan, Bharath Kumar
Wang, Hsin-Kai
Chung, Chia-Min
Lee, Chien-Hsun
Huang, Lan-Ru
Yeh, Kun-Tu
Lin, Shu-Hui
author_facet Velmurugan, Bharath Kumar
Wang, Hsin-Kai
Chung, Chia-Min
Lee, Chien-Hsun
Huang, Lan-Ru
Yeh, Kun-Tu
Lin, Shu-Hui
author_sort Velmurugan, Bharath Kumar
collection PubMed
description Introduction: Oral cancer is a prevalent form of cancer worldwide, particularly in Taiwan, and mechanisms involved in oral squamous cell carcinoma (OSCC) progression remain relatively unknown. Cancerous inhibitor of protein phosphatase 2A (CIP2A), an oncoprotein, is aberrantly expressed in many human malignant tumors including oral cancer. However, the expression and role played by CIP2A in oral cancer pathogenesis remain obscure. Methods: In this study, immunohistochemistry was used to analyze CIP2A expression between OSCC tissues and their adjacent noncancerous tissues. Furthermore, associations between CIP2A expression and histopathological parameters were investigated. Results: In this study, we showed that CIP2A was overexpressed in most of the OSCC tissues. High CIP2A expression was significantly associated with moderate/poor tumor differentiation (P=0.02). No significant association was found between CIP2A expression and other clinical parameters. Kaplan–Meier analysis revealed that high CIP2A expression showed poorer survival rates than those with low CIP2A expression (P=0.047). Multivariate Cox regression analysis indicated that CIP2A expression, N stage, American Joint Committee on Cancer stage and clinical therapy were independent prognostic factors for survival. Conclusion: Thus, our study suggests that CIP2A is an independent prognostic marker for OSCC and a novel target for OSCC treatment.
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spelling pubmed-64978562019-05-21 CIP2A overexpression in Taiwanese oral cancer patients Velmurugan, Bharath Kumar Wang, Hsin-Kai Chung, Chia-Min Lee, Chien-Hsun Huang, Lan-Ru Yeh, Kun-Tu Lin, Shu-Hui Cancer Manag Res Original Research Introduction: Oral cancer is a prevalent form of cancer worldwide, particularly in Taiwan, and mechanisms involved in oral squamous cell carcinoma (OSCC) progression remain relatively unknown. Cancerous inhibitor of protein phosphatase 2A (CIP2A), an oncoprotein, is aberrantly expressed in many human malignant tumors including oral cancer. However, the expression and role played by CIP2A in oral cancer pathogenesis remain obscure. Methods: In this study, immunohistochemistry was used to analyze CIP2A expression between OSCC tissues and their adjacent noncancerous tissues. Furthermore, associations between CIP2A expression and histopathological parameters were investigated. Results: In this study, we showed that CIP2A was overexpressed in most of the OSCC tissues. High CIP2A expression was significantly associated with moderate/poor tumor differentiation (P=0.02). No significant association was found between CIP2A expression and other clinical parameters. Kaplan–Meier analysis revealed that high CIP2A expression showed poorer survival rates than those with low CIP2A expression (P=0.047). Multivariate Cox regression analysis indicated that CIP2A expression, N stage, American Joint Committee on Cancer stage and clinical therapy were independent prognostic factors for survival. Conclusion: Thus, our study suggests that CIP2A is an independent prognostic marker for OSCC and a novel target for OSCC treatment. Dove 2019-04-05 /pmc/articles/PMC6497856/ /pubmed/31114325 http://dx.doi.org/10.2147/CMAR.S201154 Text en © 2019 Velmurugan et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Velmurugan, Bharath Kumar
Wang, Hsin-Kai
Chung, Chia-Min
Lee, Chien-Hsun
Huang, Lan-Ru
Yeh, Kun-Tu
Lin, Shu-Hui
CIP2A overexpression in Taiwanese oral cancer patients
title CIP2A overexpression in Taiwanese oral cancer patients
title_full CIP2A overexpression in Taiwanese oral cancer patients
title_fullStr CIP2A overexpression in Taiwanese oral cancer patients
title_full_unstemmed CIP2A overexpression in Taiwanese oral cancer patients
title_short CIP2A overexpression in Taiwanese oral cancer patients
title_sort cip2a overexpression in taiwanese oral cancer patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497856/
https://www.ncbi.nlm.nih.gov/pubmed/31114325
http://dx.doi.org/10.2147/CMAR.S201154
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