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Differential tissue-specific protein markers of vaginal carcinoma
The objective was to identify proteins differentially expressed in vaginal cancer to elucidate relevant cancer-related proteins. A total of 16 fresh-frozen tissue biopsies, consisting of 5 biopsies from normal vaginal epithelium, 6 from primary vaginal carcinomas and 5 from primary cervical carcinom...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2676541/ https://www.ncbi.nlm.nih.gov/pubmed/19367286 http://dx.doi.org/10.1038/sj.bjc.6604975 |
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author | Hellman, K Alaiya, A A Becker, S Lomnytska, M Schedvins, K Steinberg, W Hellström, A-C Andersson, S Hellman, U Auer, G |
author_facet | Hellman, K Alaiya, A A Becker, S Lomnytska, M Schedvins, K Steinberg, W Hellström, A-C Andersson, S Hellman, U Auer, G |
author_sort | Hellman, K |
collection | PubMed |
description | The objective was to identify proteins differentially expressed in vaginal cancer to elucidate relevant cancer-related proteins. A total of 16 fresh-frozen tissue biopsies, consisting of 5 biopsies from normal vaginal epithelium, 6 from primary vaginal carcinomas and 5 from primary cervical carcinomas, were analysed using two-dimensional gel electrophoresis (2-DE) and MALDI-TOF mass spectrometry. Of the 43 proteins identified with significant alterations in protein expression between non-tumourous and tumourous tissue, 26 were upregulated and 17 were downregulated. Some were similarly altered in vaginal and cervical carcinoma, including cytoskeletal proteins, tumour suppressor proteins, oncoproteins implicated in apoptosis and proteins in the ubiquitin–proteasome pathway. Three proteins were uniquely altered in vaginal carcinoma (DDX48, erbB3-binding protein and biliverdin reductase) and five in cervical carcinoma (peroxiredoxin 2, annexin A2, sarcomeric tropomyosin kappa, human ribonuclease inhibitor and prolyl-4-hydrolase beta). The identified proteins imply involvement of multiple different cellular pathways in the carcinogenesis of vaginal carcinoma. Similar protein alterations were found between vaginal and cervical carcinoma suggesting common tumourigenesis. However, the expression level of some of these proteins markedly differs among the three tissue specimens indicating that they might be useful molecular markers. |
format | Text |
id | pubmed-2676541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-26765412010-04-21 Differential tissue-specific protein markers of vaginal carcinoma Hellman, K Alaiya, A A Becker, S Lomnytska, M Schedvins, K Steinberg, W Hellström, A-C Andersson, S Hellman, U Auer, G Br J Cancer Molecular Diagnostics The objective was to identify proteins differentially expressed in vaginal cancer to elucidate relevant cancer-related proteins. A total of 16 fresh-frozen tissue biopsies, consisting of 5 biopsies from normal vaginal epithelium, 6 from primary vaginal carcinomas and 5 from primary cervical carcinomas, were analysed using two-dimensional gel electrophoresis (2-DE) and MALDI-TOF mass spectrometry. Of the 43 proteins identified with significant alterations in protein expression between non-tumourous and tumourous tissue, 26 were upregulated and 17 were downregulated. Some were similarly altered in vaginal and cervical carcinoma, including cytoskeletal proteins, tumour suppressor proteins, oncoproteins implicated in apoptosis and proteins in the ubiquitin–proteasome pathway. Three proteins were uniquely altered in vaginal carcinoma (DDX48, erbB3-binding protein and biliverdin reductase) and five in cervical carcinoma (peroxiredoxin 2, annexin A2, sarcomeric tropomyosin kappa, human ribonuclease inhibitor and prolyl-4-hydrolase beta). The identified proteins imply involvement of multiple different cellular pathways in the carcinogenesis of vaginal carcinoma. Similar protein alterations were found between vaginal and cervical carcinoma suggesting common tumourigenesis. However, the expression level of some of these proteins markedly differs among the three tissue specimens indicating that they might be useful molecular markers. Nature Publishing Group 2009-04-21 2009-03-24 /pmc/articles/PMC2676541/ /pubmed/19367286 http://dx.doi.org/10.1038/sj.bjc.6604975 Text en Copyright © 2009 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular Diagnostics Hellman, K Alaiya, A A Becker, S Lomnytska, M Schedvins, K Steinberg, W Hellström, A-C Andersson, S Hellman, U Auer, G Differential tissue-specific protein markers of vaginal carcinoma |
title | Differential tissue-specific protein markers of vaginal carcinoma |
title_full | Differential tissue-specific protein markers of vaginal carcinoma |
title_fullStr | Differential tissue-specific protein markers of vaginal carcinoma |
title_full_unstemmed | Differential tissue-specific protein markers of vaginal carcinoma |
title_short | Differential tissue-specific protein markers of vaginal carcinoma |
title_sort | differential tissue-specific protein markers of vaginal carcinoma |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2676541/ https://www.ncbi.nlm.nih.gov/pubmed/19367286 http://dx.doi.org/10.1038/sj.bjc.6604975 |
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