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Immunoexpression of p53 mutant-type in Iranian patients with primary and recurrence oral squamous cell carcinoma

Mutations in tumor suppressor p53 protein can occur at different phases of malignant transformation and affect the patient's prognosis. This study aimed to evaluate the expression of mutant p53 protein in Iranian patients with the primary and recurrence oral squamous cell carcinoma (OSCC). This...

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Autores principales: Daneste, Hossein, Sadeghzadeh, Azita, Mokhtari, Maral, Mohammadkhani, Hossein, Lavaee, Fatemeh, Moayedi, Javad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10141754/
http://dx.doi.org/10.4081/ejtm.2023.10847
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author Daneste, Hossein
Sadeghzadeh, Azita
Mokhtari, Maral
Mohammadkhani, Hossein
Lavaee, Fatemeh
Moayedi, Javad
author_facet Daneste, Hossein
Sadeghzadeh, Azita
Mokhtari, Maral
Mohammadkhani, Hossein
Lavaee, Fatemeh
Moayedi, Javad
author_sort Daneste, Hossein
collection PubMed
description Mutations in tumor suppressor p53 protein can occur at different phases of malignant transformation and affect the patient's prognosis. This study aimed to evaluate the expression of mutant p53 protein in Iranian patients with the primary and recurrence oral squamous cell carcinoma (OSCC). This retrospective cross-sectional study conducted on a group of patients with the primary OSCC (n=122) and the control subjects with oral noncancerous reactive lesions (n=80). Immunohistochemistry was performed with the DO-7 monoclonal antibody against p53 protein, and samples with ≥10% immunostaining were considered positive. Statistical analyses were carried out using SPSS. Positive staining for p53 was observed in none of the control subjects and 57.4% (70 of 122) of the primary OSCC patients (p<0.0001, OR=107.69, 95%CI=6.49-179.0). The p53 immunopositivity had no significant differences between males and females (54.2% vs. 62%, p=0.390), but significantly different between those aged below and over 50 years (p<0.0001, OR=4.52, 95%CI=1.07-12.05). During follow-up, OSCC recurrence occurred in 104 patients, but the phenotype of the mutant p53 protein in patients who relapsed was the same as in matched primary tumors (p=0.763). Risk of recurrence had no significant differences between p53-positive and p53-negative cases (p=0.953), males and females (p=0.263), and age below and over 50 years (p=0.223). Despite its confirmed diagnostic value, the immunoexpression of the p53 mutant protein in OSCC in cancer recurrence was the same as in the primary tumor. However, further studies with a larger sample size and longer follow-up are needed to confirm or change our conclusions.
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spelling pubmed-101417542023-04-29 Immunoexpression of p53 mutant-type in Iranian patients with primary and recurrence oral squamous cell carcinoma Daneste, Hossein Sadeghzadeh, Azita Mokhtari, Maral Mohammadkhani, Hossein Lavaee, Fatemeh Moayedi, Javad Eur J Transl Myol Article Mutations in tumor suppressor p53 protein can occur at different phases of malignant transformation and affect the patient's prognosis. This study aimed to evaluate the expression of mutant p53 protein in Iranian patients with the primary and recurrence oral squamous cell carcinoma (OSCC). This retrospective cross-sectional study conducted on a group of patients with the primary OSCC (n=122) and the control subjects with oral noncancerous reactive lesions (n=80). Immunohistochemistry was performed with the DO-7 monoclonal antibody against p53 protein, and samples with ≥10% immunostaining were considered positive. Statistical analyses were carried out using SPSS. Positive staining for p53 was observed in none of the control subjects and 57.4% (70 of 122) of the primary OSCC patients (p<0.0001, OR=107.69, 95%CI=6.49-179.0). The p53 immunopositivity had no significant differences between males and females (54.2% vs. 62%, p=0.390), but significantly different between those aged below and over 50 years (p<0.0001, OR=4.52, 95%CI=1.07-12.05). During follow-up, OSCC recurrence occurred in 104 patients, but the phenotype of the mutant p53 protein in patients who relapsed was the same as in matched primary tumors (p=0.763). Risk of recurrence had no significant differences between p53-positive and p53-negative cases (p=0.953), males and females (p=0.263), and age below and over 50 years (p=0.223). Despite its confirmed diagnostic value, the immunoexpression of the p53 mutant protein in OSCC in cancer recurrence was the same as in the primary tumor. However, further studies with a larger sample size and longer follow-up are needed to confirm or change our conclusions. PAGEPress Publications, Pavia, Italy 2022-11-22 /pmc/articles/PMC10141754/ http://dx.doi.org/10.4081/ejtm.2023.10847 Text en https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Article
Daneste, Hossein
Sadeghzadeh, Azita
Mokhtari, Maral
Mohammadkhani, Hossein
Lavaee, Fatemeh
Moayedi, Javad
Immunoexpression of p53 mutant-type in Iranian patients with primary and recurrence oral squamous cell carcinoma
title Immunoexpression of p53 mutant-type in Iranian patients with primary and recurrence oral squamous cell carcinoma
title_full Immunoexpression of p53 mutant-type in Iranian patients with primary and recurrence oral squamous cell carcinoma
title_fullStr Immunoexpression of p53 mutant-type in Iranian patients with primary and recurrence oral squamous cell carcinoma
title_full_unstemmed Immunoexpression of p53 mutant-type in Iranian patients with primary and recurrence oral squamous cell carcinoma
title_short Immunoexpression of p53 mutant-type in Iranian patients with primary and recurrence oral squamous cell carcinoma
title_sort immunoexpression of p53 mutant-type in iranian patients with primary and recurrence oral squamous cell carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10141754/
http://dx.doi.org/10.4081/ejtm.2023.10847
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