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Screening and functional analysis of a differential protein profile of human breast cancer

To improve the understanding of the enriched functions of proteins and to identify potential biomarkers in human breast cancer, the present study constructed a differentially expressed protein profile by screening immunohistochemistry maps of human breast cancer proteins. A total of 1,688 proteins w...

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Detalles Bibliográficos
Autores principales: LIU, FU-JUN, WANG, XUE-BO, CAO, AI-GUO
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049688/
https://www.ncbi.nlm.nih.gov/pubmed/24932247
http://dx.doi.org/10.3892/ol.2014.1978
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author LIU, FU-JUN
WANG, XUE-BO
CAO, AI-GUO
author_facet LIU, FU-JUN
WANG, XUE-BO
CAO, AI-GUO
author_sort LIU, FU-JUN
collection PubMed
description To improve the understanding of the enriched functions of proteins and to identify potential biomarkers in human breast cancer, the present study constructed a differentially expressed protein profile by screening immunohistochemistry maps of human breast cancer proteins. A total of 1,688 proteins were found to be differentially expressed in human breast cancer, including 773 upregulated and 915 downregulated proteins. Of these proteins, secreted and membrane proteins were screened and clustered, and more enriched biological functions and pathways were presented in the upregulated protein profiles. Furthermore, altered serum levels of peroxiredoxin (PRDX)2, PRDX6, cathepsin (CTS)B and CTSD were detected by ELISA assay. The present study provides a novel global mapping of potential breast cancer biomarkers that could be used as background to identify the altered pathways in human breast cancer, as well as potential cancer targets.
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spelling pubmed-40496882014-06-13 Screening and functional analysis of a differential protein profile of human breast cancer LIU, FU-JUN WANG, XUE-BO CAO, AI-GUO Oncol Lett Articles To improve the understanding of the enriched functions of proteins and to identify potential biomarkers in human breast cancer, the present study constructed a differentially expressed protein profile by screening immunohistochemistry maps of human breast cancer proteins. A total of 1,688 proteins were found to be differentially expressed in human breast cancer, including 773 upregulated and 915 downregulated proteins. Of these proteins, secreted and membrane proteins were screened and clustered, and more enriched biological functions and pathways were presented in the upregulated protein profiles. Furthermore, altered serum levels of peroxiredoxin (PRDX)2, PRDX6, cathepsin (CTS)B and CTSD were detected by ELISA assay. The present study provides a novel global mapping of potential breast cancer biomarkers that could be used as background to identify the altered pathways in human breast cancer, as well as potential cancer targets. D.A. Spandidos 2014-06 2014-03-18 /pmc/articles/PMC4049688/ /pubmed/24932247 http://dx.doi.org/10.3892/ol.2014.1978 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
LIU, FU-JUN
WANG, XUE-BO
CAO, AI-GUO
Screening and functional analysis of a differential protein profile of human breast cancer
title Screening and functional analysis of a differential protein profile of human breast cancer
title_full Screening and functional analysis of a differential protein profile of human breast cancer
title_fullStr Screening and functional analysis of a differential protein profile of human breast cancer
title_full_unstemmed Screening and functional analysis of a differential protein profile of human breast cancer
title_short Screening and functional analysis of a differential protein profile of human breast cancer
title_sort screening and functional analysis of a differential protein profile of human breast cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049688/
https://www.ncbi.nlm.nih.gov/pubmed/24932247
http://dx.doi.org/10.3892/ol.2014.1978
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