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Status of p53 and p27(KIP1) in Iranian Patients With Oral Squamous Cell Carcinoma

BACKGROUND: Alterations in p53 and p27(KIP1) have been documented as important events in the carcinogenesis of various cancers, but their prognostic role in oral squamous cell carcinoma (OSCC) remains controversial. OBJECTIVES: The present investigation aimed to evaluate the clinicopathologic and pr...

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Autores principales: Etemad-Moghadam, Shahroo, Keyhani, Amanollah, Yazdani, Kamran, Alaeddini, Mojgan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640065/
https://www.ncbi.nlm.nih.gov/pubmed/26568852
http://dx.doi.org/10.5812/ircmj.19359
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author Etemad-Moghadam, Shahroo
Keyhani, Amanollah
Yazdani, Kamran
Alaeddini, Mojgan
author_facet Etemad-Moghadam, Shahroo
Keyhani, Amanollah
Yazdani, Kamran
Alaeddini, Mojgan
author_sort Etemad-Moghadam, Shahroo
collection PubMed
description BACKGROUND: Alterations in p53 and p27(KIP1) have been documented as important events in the carcinogenesis of various cancers, but their prognostic role in oral squamous cell carcinoma (OSCC) remains controversial. OBJECTIVES: The present investigation aimed to evaluate the clinicopathologic and prognostic significance of p53 and p27(KIP1) expression in a group of Iranian patients with OSCC. PATIENTS AND METHODS: In this analytical cross-sectional study, medical records of patients with primary OSCC, diagnosed from 1994 to 2004 were reviewed and 28 subjects were selected based on the inclusion/exclusion criteria. Immunohistochemical staining using monoclonal antibodies against p53 and p27(KIP1) was performed on representative archival paraffin blocks. Demographic data along with information on p53 and p27(KIP1) expression, recurrence, and tumor grade was statistically analyzed using the Fischer exact test. Prognostic factors for overall survival were determined by Cox regression analysis (P < 0.05). RESULTS: p53 and p27(KIP1) expression were found in 28.57% (8 positive versus 20 negative) and 67.85% (19 positive versus 9 negative) of OSCC cases, respectively. There was no significant association between these two proteins (P = 0.371), and neither of them showed a significant relationship with the studied clinicopathologic variables (P > 0.05). In survival analysis, only histopathologic differentiation (17 low and moderate, 11 poor) demonstrated a significant correlation with overall survival (P = 0.048). CONCLUSIONS: Despite the fact that abnormalities in p53 and p27(KIP1) may be involved in the development of OSCC, their clinical significance in the studied population seems limited. Further investigation on the combined p53/p27(KIP1) expression may be helpful in predicting the biologic behavior of this tumor.
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spelling pubmed-46400652015-11-13 Status of p53 and p27(KIP1) in Iranian Patients With Oral Squamous Cell Carcinoma Etemad-Moghadam, Shahroo Keyhani, Amanollah Yazdani, Kamran Alaeddini, Mojgan Iran Red Crescent Med J Research Article BACKGROUND: Alterations in p53 and p27(KIP1) have been documented as important events in the carcinogenesis of various cancers, but their prognostic role in oral squamous cell carcinoma (OSCC) remains controversial. OBJECTIVES: The present investigation aimed to evaluate the clinicopathologic and prognostic significance of p53 and p27(KIP1) expression in a group of Iranian patients with OSCC. PATIENTS AND METHODS: In this analytical cross-sectional study, medical records of patients with primary OSCC, diagnosed from 1994 to 2004 were reviewed and 28 subjects were selected based on the inclusion/exclusion criteria. Immunohistochemical staining using monoclonal antibodies against p53 and p27(KIP1) was performed on representative archival paraffin blocks. Demographic data along with information on p53 and p27(KIP1) expression, recurrence, and tumor grade was statistically analyzed using the Fischer exact test. Prognostic factors for overall survival were determined by Cox regression analysis (P < 0.05). RESULTS: p53 and p27(KIP1) expression were found in 28.57% (8 positive versus 20 negative) and 67.85% (19 positive versus 9 negative) of OSCC cases, respectively. There was no significant association between these two proteins (P = 0.371), and neither of them showed a significant relationship with the studied clinicopathologic variables (P > 0.05). In survival analysis, only histopathologic differentiation (17 low and moderate, 11 poor) demonstrated a significant correlation with overall survival (P = 0.048). CONCLUSIONS: Despite the fact that abnormalities in p53 and p27(KIP1) may be involved in the development of OSCC, their clinical significance in the studied population seems limited. Further investigation on the combined p53/p27(KIP1) expression may be helpful in predicting the biologic behavior of this tumor. Kowsar 2015-10-19 /pmc/articles/PMC4640065/ /pubmed/26568852 http://dx.doi.org/10.5812/ircmj.19359 Text en Copyright © 2015, Iranian Red Crescent Medical Journal. http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Research Article
Etemad-Moghadam, Shahroo
Keyhani, Amanollah
Yazdani, Kamran
Alaeddini, Mojgan
Status of p53 and p27(KIP1) in Iranian Patients With Oral Squamous Cell Carcinoma
title Status of p53 and p27(KIP1) in Iranian Patients With Oral Squamous Cell Carcinoma
title_full Status of p53 and p27(KIP1) in Iranian Patients With Oral Squamous Cell Carcinoma
title_fullStr Status of p53 and p27(KIP1) in Iranian Patients With Oral Squamous Cell Carcinoma
title_full_unstemmed Status of p53 and p27(KIP1) in Iranian Patients With Oral Squamous Cell Carcinoma
title_short Status of p53 and p27(KIP1) in Iranian Patients With Oral Squamous Cell Carcinoma
title_sort status of p53 and p27(kip1) in iranian patients with oral squamous cell carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640065/
https://www.ncbi.nlm.nih.gov/pubmed/26568852
http://dx.doi.org/10.5812/ircmj.19359
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