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Hsp74, a Potential Bladder Cancer Marker, Has Direct Interaction with Keratin 1
Early diagnosis and prognosis monitoring are very important for the survival of patients with bladder cancer. To identify candidate biomarkers of bladder cancer, we used a combination of techniques including 2-DE, co-IP, western blot, LC-MS/MS, and immunohistochemistry. Hsp74 was identified with hig...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094855/ https://www.ncbi.nlm.nih.gov/pubmed/25050384 http://dx.doi.org/10.1155/2014/492849 |
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author | Chen, Ling Wang, YaRong Zhao, Le Chen, Wei Dong, Chunhui Zhao, Xinhan Li, Xu |
author_facet | Chen, Ling Wang, YaRong Zhao, Le Chen, Wei Dong, Chunhui Zhao, Xinhan Li, Xu |
author_sort | Chen, Ling |
collection | PubMed |
description | Early diagnosis and prognosis monitoring are very important for the survival of patients with bladder cancer. To identify candidate biomarkers of bladder cancer, we used a combination of techniques including 2-DE, co-IP, western blot, LC-MS/MS, and immunohistochemistry. Hsp74 was identified with high expression in bladder cancer. The cellular location of expression products of gene Hsp74 showed that they were distributed into cytoplasm and keratin 1 was found to be associated with Hsp74. The results provide a new idea to understand the molecular basis of bladder cancer progression and pinpoint new potential molecular target for early diagnosis and therapeutic monitoring of bladder cancer. |
format | Online Article Text |
id | pubmed-4094855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-40948552014-07-21 Hsp74, a Potential Bladder Cancer Marker, Has Direct Interaction with Keratin 1 Chen, Ling Wang, YaRong Zhao, Le Chen, Wei Dong, Chunhui Zhao, Xinhan Li, Xu J Immunol Res Research Article Early diagnosis and prognosis monitoring are very important for the survival of patients with bladder cancer. To identify candidate biomarkers of bladder cancer, we used a combination of techniques including 2-DE, co-IP, western blot, LC-MS/MS, and immunohistochemistry. Hsp74 was identified with high expression in bladder cancer. The cellular location of expression products of gene Hsp74 showed that they were distributed into cytoplasm and keratin 1 was found to be associated with Hsp74. The results provide a new idea to understand the molecular basis of bladder cancer progression and pinpoint new potential molecular target for early diagnosis and therapeutic monitoring of bladder cancer. Hindawi Publishing Corporation 2014 2014-06-23 /pmc/articles/PMC4094855/ /pubmed/25050384 http://dx.doi.org/10.1155/2014/492849 Text en Copyright © 2014 Ling Chen et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Chen, Ling Wang, YaRong Zhao, Le Chen, Wei Dong, Chunhui Zhao, Xinhan Li, Xu Hsp74, a Potential Bladder Cancer Marker, Has Direct Interaction with Keratin 1 |
title | Hsp74, a Potential Bladder Cancer Marker, Has Direct Interaction with Keratin 1 |
title_full | Hsp74, a Potential Bladder Cancer Marker, Has Direct Interaction with Keratin 1 |
title_fullStr | Hsp74, a Potential Bladder Cancer Marker, Has Direct Interaction with Keratin 1 |
title_full_unstemmed | Hsp74, a Potential Bladder Cancer Marker, Has Direct Interaction with Keratin 1 |
title_short | Hsp74, a Potential Bladder Cancer Marker, Has Direct Interaction with Keratin 1 |
title_sort | hsp74, a potential bladder cancer marker, has direct interaction with keratin 1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094855/ https://www.ncbi.nlm.nih.gov/pubmed/25050384 http://dx.doi.org/10.1155/2014/492849 |
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