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p53 and PTEN expression evaluation with molecular evident recent criteria in laryngeal carcinoma
The prognosis of laryngeal cancer is affected by clinicopathological factors. Because of that, an effective prognostic marker is very valuable in managing the clinical process. The p53 evaluation method, used in the literature recently, was used for the first time in laryngeal cancer. We evaluated P...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174377/ https://www.ncbi.nlm.nih.gov/pubmed/37171328 http://dx.doi.org/10.1097/MD.0000000000033676 |
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author | Tan, Ayca Eskiizmir, Gorkem Kamiloglu, Ugur Sarioglu, Sulen |
author_facet | Tan, Ayca Eskiizmir, Gorkem Kamiloglu, Ugur Sarioglu, Sulen |
author_sort | Tan, Ayca |
collection | PubMed |
description | The prognosis of laryngeal cancer is affected by clinicopathological factors. Because of that, an effective prognostic marker is very valuable in managing the clinical process. The p53 evaluation method, used in the literature recently, was used for the first time in laryngeal cancer. We evaluated PTEN with 2 methods with the highest significance in the literature on laryngeal cancer. All demographic and histopathological data from 140 laryngeal cancers were compared with p53 and PTEN expressions and survival. p53 staining patterns were classified as wild and mutant. PTEN expression was evaluated according to the staining intensity named PTEN1 and according to the proportion of stained cells named PTEN2. In the series, 93.6% were males, and the mean survival was 38 months. 69.3% of cases were p53 mutants. PTEN loss was found to be 85.7% and 57.9%, respectively. Tumor size and thyroid cartilage invasion for PTEN1 and age for p53 were identified as independent predictive factors (P < .01). Advanced age, total laryngectomy, and extranodal spread were independent poor prognostic factors for overall survival and the presence of subglottic involvement, perineural invasion, and extranodal spread were for disease-free survival (P < .01). This is the first study in which the new p53 classification was used in laryngeal cancer, and will contribute significantly to the literature with differences from the previous evaluation patterns. Evaluation of PTEN based on staining intensity is more appropriate compared to the percentage of stained cells. |
format | Online Article Text |
id | pubmed-10174377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-101743772023-05-12 p53 and PTEN expression evaluation with molecular evident recent criteria in laryngeal carcinoma Tan, Ayca Eskiizmir, Gorkem Kamiloglu, Ugur Sarioglu, Sulen Medicine (Baltimore) 6000 The prognosis of laryngeal cancer is affected by clinicopathological factors. Because of that, an effective prognostic marker is very valuable in managing the clinical process. The p53 evaluation method, used in the literature recently, was used for the first time in laryngeal cancer. We evaluated PTEN with 2 methods with the highest significance in the literature on laryngeal cancer. All demographic and histopathological data from 140 laryngeal cancers were compared with p53 and PTEN expressions and survival. p53 staining patterns were classified as wild and mutant. PTEN expression was evaluated according to the staining intensity named PTEN1 and according to the proportion of stained cells named PTEN2. In the series, 93.6% were males, and the mean survival was 38 months. 69.3% of cases were p53 mutants. PTEN loss was found to be 85.7% and 57.9%, respectively. Tumor size and thyroid cartilage invasion for PTEN1 and age for p53 were identified as independent predictive factors (P < .01). Advanced age, total laryngectomy, and extranodal spread were independent poor prognostic factors for overall survival and the presence of subglottic involvement, perineural invasion, and extranodal spread were for disease-free survival (P < .01). This is the first study in which the new p53 classification was used in laryngeal cancer, and will contribute significantly to the literature with differences from the previous evaluation patterns. Evaluation of PTEN based on staining intensity is more appropriate compared to the percentage of stained cells. Lippincott Williams & Wilkins 2023-05-12 /pmc/articles/PMC10174377/ /pubmed/37171328 http://dx.doi.org/10.1097/MD.0000000000033676 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. |
spellingShingle | 6000 Tan, Ayca Eskiizmir, Gorkem Kamiloglu, Ugur Sarioglu, Sulen p53 and PTEN expression evaluation with molecular evident recent criteria in laryngeal carcinoma |
title | p53 and PTEN expression evaluation with molecular evident recent criteria in laryngeal carcinoma |
title_full | p53 and PTEN expression evaluation with molecular evident recent criteria in laryngeal carcinoma |
title_fullStr | p53 and PTEN expression evaluation with molecular evident recent criteria in laryngeal carcinoma |
title_full_unstemmed | p53 and PTEN expression evaluation with molecular evident recent criteria in laryngeal carcinoma |
title_short | p53 and PTEN expression evaluation with molecular evident recent criteria in laryngeal carcinoma |
title_sort | p53 and pten expression evaluation with molecular evident recent criteria in laryngeal carcinoma |
topic | 6000 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174377/ https://www.ncbi.nlm.nih.gov/pubmed/37171328 http://dx.doi.org/10.1097/MD.0000000000033676 |
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