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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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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. |
format | Online Article Text |
id | pubmed-6497856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
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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