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Gasdermin D: A potential mediator and prognostic marker of bladder cancer

Background: Bladder cancer is considered one of the commonest widespread cancers, its presentation ranges from non-muscle invasive form to being muscle-invasive. The gasdermin family of proteins consists of six proteins. Members of gasdermin family are involved in pyroptosis; which is considered as...

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Autores principales: El-Gamal, Randa, Abdelrahim, Mona, El-Sherbiny, Mohamed, Enan, Eman T., El-Nablaway, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474890/
https://www.ncbi.nlm.nih.gov/pubmed/36120543
http://dx.doi.org/10.3389/fmolb.2022.972087
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author El-Gamal, Randa
Abdelrahim, Mona
El-Sherbiny, Mohamed
Enan, Eman T.
El-Nablaway, Mohammad
author_facet El-Gamal, Randa
Abdelrahim, Mona
El-Sherbiny, Mohamed
Enan, Eman T.
El-Nablaway, Mohammad
author_sort El-Gamal, Randa
collection PubMed
description Background: Bladder cancer is considered one of the commonest widespread cancers, its presentation ranges from non-muscle invasive form to being muscle-invasive. The gasdermin family of proteins consists of six proteins. Members of gasdermin family are involved in pyroptosis; which is considered as type of inflammatory apoptosis via participation of gasdermin D and inflammatory caspases. Purpose: The goal of this research was to look into the potential involvement of gasdermin D in pathogenesis of bladder cancer, In addition, to investigate its potential role as a prognostic marker of bladder cancer. Methods: Gasdermin D gene and protein expression was examined in fresh frozen 80 bladder cancer specimens (30 NMIBC, and 50 MIBC) and the matching 80 control tissue samples utilizing real-time polymerase chain reaction and western blotting. Furthermore, the immunoreactivity of gasdermin D protein was also detected by immunohistochemistry. Results: Gasdermin D gene and protein expression showed a highly significant difference between the control and the two bladder cancer groups (p < 0.001), as demonstrated by real-time PCR, western blotting and immunohistochemistry. Cox proportional hazards regression models showed that lower gasdermin D gene expression in cancer patients (≤1.58-fold), and younger age (≤53 years) were linked with a higher risk of local tumor recurrence. Moreover, higher gasdermin D gene expression (>2.18-fold), and lymph nodes’ involvement were associated with an increased mortality. Conclusion: Gasdermin D is involved in the pathogenesis of bladder cancer and muscle invasion, in addition, tissue gasdermin D expression may be used as useful tool to predict local tumor recurrence.
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spelling pubmed-94748902022-09-16 Gasdermin D: A potential mediator and prognostic marker of bladder cancer El-Gamal, Randa Abdelrahim, Mona El-Sherbiny, Mohamed Enan, Eman T. El-Nablaway, Mohammad Front Mol Biosci Molecular Biosciences Background: Bladder cancer is considered one of the commonest widespread cancers, its presentation ranges from non-muscle invasive form to being muscle-invasive. The gasdermin family of proteins consists of six proteins. Members of gasdermin family are involved in pyroptosis; which is considered as type of inflammatory apoptosis via participation of gasdermin D and inflammatory caspases. Purpose: The goal of this research was to look into the potential involvement of gasdermin D in pathogenesis of bladder cancer, In addition, to investigate its potential role as a prognostic marker of bladder cancer. Methods: Gasdermin D gene and protein expression was examined in fresh frozen 80 bladder cancer specimens (30 NMIBC, and 50 MIBC) and the matching 80 control tissue samples utilizing real-time polymerase chain reaction and western blotting. Furthermore, the immunoreactivity of gasdermin D protein was also detected by immunohistochemistry. Results: Gasdermin D gene and protein expression showed a highly significant difference between the control and the two bladder cancer groups (p < 0.001), as demonstrated by real-time PCR, western blotting and immunohistochemistry. Cox proportional hazards regression models showed that lower gasdermin D gene expression in cancer patients (≤1.58-fold), and younger age (≤53 years) were linked with a higher risk of local tumor recurrence. Moreover, higher gasdermin D gene expression (>2.18-fold), and lymph nodes’ involvement were associated with an increased mortality. Conclusion: Gasdermin D is involved in the pathogenesis of bladder cancer and muscle invasion, in addition, tissue gasdermin D expression may be used as useful tool to predict local tumor recurrence. Frontiers Media S.A. 2022-09-01 /pmc/articles/PMC9474890/ /pubmed/36120543 http://dx.doi.org/10.3389/fmolb.2022.972087 Text en Copyright © 2022 El-Gamal, Abdelrahim, El-Sherbiny, Enan and El-Nablaway. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Biosciences
El-Gamal, Randa
Abdelrahim, Mona
El-Sherbiny, Mohamed
Enan, Eman T.
El-Nablaway, Mohammad
Gasdermin D: A potential mediator and prognostic marker of bladder cancer
title Gasdermin D: A potential mediator and prognostic marker of bladder cancer
title_full Gasdermin D: A potential mediator and prognostic marker of bladder cancer
title_fullStr Gasdermin D: A potential mediator and prognostic marker of bladder cancer
title_full_unstemmed Gasdermin D: A potential mediator and prognostic marker of bladder cancer
title_short Gasdermin D: A potential mediator and prognostic marker of bladder cancer
title_sort gasdermin d: a potential mediator and prognostic marker of bladder cancer
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474890/
https://www.ncbi.nlm.nih.gov/pubmed/36120543
http://dx.doi.org/10.3389/fmolb.2022.972087
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