Cargando…

Remodeling Factors, Transcription Factors and Angiogenetic Factors in Cholesteatoma in Ontogenetic Aspect

INTRODUCTION: The main goal of our study was to describe the transcription factor (NF-κβ), angiogenetic factor (VEGF), and remodeling markers (MMP-9 and TIMP-4) of the cholesteatoma tissue compared to control skin tissue. There are still uncertainties how transcription, angiogenetic and remodeling f...

Descripción completa

Detalles Bibliográficos
Autores principales: Dambergs, Kristaps, Sumeraga, Gunta, Pilmane, Māra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9119338/
https://www.ncbi.nlm.nih.gov/pubmed/35655767
http://dx.doi.org/10.22038/IJORL.2021.53716.2842
_version_ 1784710682533429248
author Dambergs, Kristaps
Sumeraga, Gunta
Pilmane, Māra
author_facet Dambergs, Kristaps
Sumeraga, Gunta
Pilmane, Māra
author_sort Dambergs, Kristaps
collection PubMed
description INTRODUCTION: The main goal of our study was to describe the transcription factor (NF-κβ), angiogenetic factor (VEGF), and remodeling markers (MMP-9 and TIMP-4) of the cholesteatoma tissue compared to control skin tissue. There are still uncertainties how transcription, angiogenetic and remodeling factors affect the cholesteatoma course. MATERIALS AND METHODS: Eight cholesteatoma tissue specimens were retrieved from children, seven – from adults, seven skin controls – from cadavers. Obtained material immunohistochemically were stained for NF-κβ, MMP-9, TIMP-4, VEGF. Non-parametric statistic methods were used. RESULTS: A statistically significant higher numbers of NF-κβ and TIMP-4 immunoreactive cells in the cholesteatoma compared to control group. A very strong positive correlation between MMP-9 and TIMP-4 was seen in the patient group. A strong positive correlation - between MMP-9 in matrix and MMP-9, VEGF in perimatrix, between TIMP-4 in matrix and TIMP-4 in perimatrix, NF-κβ in the matrix and VEGF; between TIMP-4 in perimatrix and NF-κβ in the matrix. CONCLUSIONS: Correlation between MMP-9 and TIMP-4 suggests that TIMP-4 in cholesteatoma tissue intercorrelates to MMP-9. TIMP-4 likely regulates the development of cholesteatoma. Disbalance between MMPs and TIMPs affects NF-κβ and causes uncontrolled cell proliferation and immune response in this tumor. There is a lack of VEGF strong expression in cholesteatoma perimatrix.
format Online
Article
Text
id pubmed-9119338
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Mashhad University of Medical Sciences
record_format MEDLINE/PubMed
spelling pubmed-91193382022-06-01 Remodeling Factors, Transcription Factors and Angiogenetic Factors in Cholesteatoma in Ontogenetic Aspect Dambergs, Kristaps Sumeraga, Gunta Pilmane, Māra Iran J Otorhinolaryngol Original Article INTRODUCTION: The main goal of our study was to describe the transcription factor (NF-κβ), angiogenetic factor (VEGF), and remodeling markers (MMP-9 and TIMP-4) of the cholesteatoma tissue compared to control skin tissue. There are still uncertainties how transcription, angiogenetic and remodeling factors affect the cholesteatoma course. MATERIALS AND METHODS: Eight cholesteatoma tissue specimens were retrieved from children, seven – from adults, seven skin controls – from cadavers. Obtained material immunohistochemically were stained for NF-κβ, MMP-9, TIMP-4, VEGF. Non-parametric statistic methods were used. RESULTS: A statistically significant higher numbers of NF-κβ and TIMP-4 immunoreactive cells in the cholesteatoma compared to control group. A very strong positive correlation between MMP-9 and TIMP-4 was seen in the patient group. A strong positive correlation - between MMP-9 in matrix and MMP-9, VEGF in perimatrix, between TIMP-4 in matrix and TIMP-4 in perimatrix, NF-κβ in the matrix and VEGF; between TIMP-4 in perimatrix and NF-κβ in the matrix. CONCLUSIONS: Correlation between MMP-9 and TIMP-4 suggests that TIMP-4 in cholesteatoma tissue intercorrelates to MMP-9. TIMP-4 likely regulates the development of cholesteatoma. Disbalance between MMPs and TIMPs affects NF-κβ and causes uncontrolled cell proliferation and immune response in this tumor. There is a lack of VEGF strong expression in cholesteatoma perimatrix. Mashhad University of Medical Sciences 2022-03 /pmc/articles/PMC9119338/ /pubmed/35655767 http://dx.doi.org/10.22038/IJORL.2021.53716.2842 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Dambergs, Kristaps
Sumeraga, Gunta
Pilmane, Māra
Remodeling Factors, Transcription Factors and Angiogenetic Factors in Cholesteatoma in Ontogenetic Aspect
title Remodeling Factors, Transcription Factors and Angiogenetic Factors in Cholesteatoma in Ontogenetic Aspect
title_full Remodeling Factors, Transcription Factors and Angiogenetic Factors in Cholesteatoma in Ontogenetic Aspect
title_fullStr Remodeling Factors, Transcription Factors and Angiogenetic Factors in Cholesteatoma in Ontogenetic Aspect
title_full_unstemmed Remodeling Factors, Transcription Factors and Angiogenetic Factors in Cholesteatoma in Ontogenetic Aspect
title_short Remodeling Factors, Transcription Factors and Angiogenetic Factors in Cholesteatoma in Ontogenetic Aspect
title_sort remodeling factors, transcription factors and angiogenetic factors in cholesteatoma in ontogenetic aspect
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9119338/
https://www.ncbi.nlm.nih.gov/pubmed/35655767
http://dx.doi.org/10.22038/IJORL.2021.53716.2842
work_keys_str_mv AT dambergskristaps remodelingfactorstranscriptionfactorsandangiogeneticfactorsincholesteatomainontogeneticaspect
AT sumeragagunta remodelingfactorstranscriptionfactorsandangiogeneticfactorsincholesteatomainontogeneticaspect
AT pilmanemara remodelingfactorstranscriptionfactorsandangiogeneticfactorsincholesteatomainontogeneticaspect