Upregulation of Phosphorylated HSP27, PRDX2, GRP75, GRP78 and GRP94 in Acquired Middle Ear Cholesteatoma Growth
Cholesteatoma is a destructive and expanding growth of keratinizing squamous epithelium in the middle ear or petrous apex. The molecular and cellular processes of the pathogenesis of acquired middle ear cholesteatoma have not been fully understood. In this study, comparative proteomic analysis was c...
Main Authors: | , , , , , , , , , , |
---|---|
Format: | Online |
Language: | English |
Published: |
Molecular Diversity Preservation International (MDPI)
2013
|
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3742253/ |
id |
pubmed-3742253 |
---|---|
recordtype |
oai_dc |
spelling |
pubmed-37422532013-08-13 Upregulation of Phosphorylated HSP27, PRDX2, GRP75, GRP78 and GRP94 in Acquired Middle Ear Cholesteatoma Growth Ho, Kuen Yao Yeh, Tai Sheng Huang, Han Hsiang Hung, Kuo Feng Chai, Chee Yin Chen, Wan Tzu Tsai, Shih Meng Chang, Ning Chia Chien, Chen Yu Wang, Hsun Mo Wu, Yu Jen Article Cholesteatoma is a destructive and expanding growth of keratinizing squamous epithelium in the middle ear or petrous apex. The molecular and cellular processes of the pathogenesis of acquired middle ear cholesteatoma have not been fully understood. In this study, comparative proteomic analysis was conducted to investigate the roles of specific proteins in the pathways regarding keratinocyte proliferation in cholesteatoma. The differential proteins were detected by comparing the two-dimension electrophoresis (2-DE) maps of the epithelial tissues of 12 attic cholesteatomas with those of retroauricular skins. There were 14 upregulated proteins in the epithelial tissues of cholesteatoma in comparison with retroauricular skin. The modulation of five crucial proteins, HSP27, PRDX2, GRP75, GRP78 and GRP94, was further determined by RT-PCR, Western blot and immunohistochemistry. Phosphorylation of HSP27 at Ser-82 was identified by mass spectroscopy. The results of this study suggested that phosphorylated HSP27 is the end expression of two potential signal-transduction pathways, and together with PRDX2, they are very likely involved in the proliferation of keratinocytes in cholesteatoma. Upregulations of GRP75, GRP78 and GRP94 in keratinocytes may be able to counter endoplasmic reticulum stress, to inhibit cell apoptosis, to prevent protein unfolding and to promote cholesteatoma growth. Molecular Diversity Preservation International (MDPI) 2013-07-11 /pmc/articles/PMC3742253/ /pubmed/23852020 http://dx.doi.org/10.3390/ijms140714439 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Ho, Kuen Yao Yeh, Tai Sheng Huang, Han Hsiang Hung, Kuo Feng Chai, Chee Yin Chen, Wan Tzu Tsai, Shih Meng Chang, Ning Chia Chien, Chen Yu Wang, Hsun Mo Wu, Yu Jen |
spellingShingle |
Ho, Kuen Yao Yeh, Tai Sheng Huang, Han Hsiang Hung, Kuo Feng Chai, Chee Yin Chen, Wan Tzu Tsai, Shih Meng Chang, Ning Chia Chien, Chen Yu Wang, Hsun Mo Wu, Yu Jen Upregulation of Phosphorylated HSP27, PRDX2, GRP75, GRP78 and GRP94 in Acquired Middle Ear Cholesteatoma Growth |
author_facet |
Ho, Kuen Yao Yeh, Tai Sheng Huang, Han Hsiang Hung, Kuo Feng Chai, Chee Yin Chen, Wan Tzu Tsai, Shih Meng Chang, Ning Chia Chien, Chen Yu Wang, Hsun Mo Wu, Yu Jen |
author_sort |
Ho, Kuen Yao |
title |
Upregulation of Phosphorylated HSP27, PRDX2, GRP75, GRP78 and GRP94 in Acquired Middle Ear Cholesteatoma Growth |
title_short |
Upregulation of Phosphorylated HSP27, PRDX2, GRP75, GRP78 and GRP94 in Acquired Middle Ear Cholesteatoma Growth |
title_full |
Upregulation of Phosphorylated HSP27, PRDX2, GRP75, GRP78 and GRP94 in Acquired Middle Ear Cholesteatoma Growth |
title_fullStr |
Upregulation of Phosphorylated HSP27, PRDX2, GRP75, GRP78 and GRP94 in Acquired Middle Ear Cholesteatoma Growth |
title_full_unstemmed |
Upregulation of Phosphorylated HSP27, PRDX2, GRP75, GRP78 and GRP94 in Acquired Middle Ear Cholesteatoma Growth |
title_sort |
upregulation of phosphorylated hsp27, prdx2, grp75, grp78 and grp94 in acquired middle ear cholesteatoma growth |
description |
Cholesteatoma is a destructive and expanding growth of keratinizing squamous epithelium in the middle ear or petrous apex. The molecular and cellular processes of the pathogenesis of acquired middle ear cholesteatoma have not been fully understood. In this study, comparative proteomic analysis was conducted to investigate the roles of specific proteins in the pathways regarding keratinocyte proliferation in cholesteatoma. The differential proteins were detected by comparing the two-dimension electrophoresis (2-DE) maps of the epithelial tissues of 12 attic cholesteatomas with those of retroauricular skins. There were 14 upregulated proteins in the epithelial tissues of cholesteatoma in comparison with retroauricular skin. The modulation of five crucial proteins, HSP27, PRDX2, GRP75, GRP78 and GRP94, was further determined by RT-PCR, Western blot and immunohistochemistry. Phosphorylation of HSP27 at Ser-82 was identified by mass spectroscopy. The results of this study suggested that phosphorylated HSP27 is the end expression of two potential signal-transduction pathways, and together with PRDX2, they are very likely involved in the proliferation of keratinocytes in cholesteatoma. Upregulations of GRP75, GRP78 and GRP94 in keratinocytes may be able to counter endoplasmic reticulum stress, to inhibit cell apoptosis, to prevent protein unfolding and to promote cholesteatoma growth. |
publisher |
Molecular Diversity Preservation International (MDPI) |
publishDate |
2013 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3742253/ |
_version_ |
1612002753615233024 |