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Grading Breast Cancer Tissues Using Molecular Portraits

Tumor progression and prognosis in breast cancer patients are difficult to assess using current clinical and laboratory parameters, where a pathological grading is indicative of tumor aggressiveness. This grading is based on assessments of nuclear grade, tubule formation, and mitotic rate. We report...

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Autores principales: Olsson, Niclas, Carlsson, Petter, James, Peter, Hansson, Karin, Waldemarson, Sofia, Malmström, Per, Fernö, Mårten, Ryden, Lisa, Wingren, Christer, Borrebaeck, Carl A. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Biochemistry and Molecular Biology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3861711/
https://www.ncbi.nlm.nih.gov/pubmed/23982162
http://dx.doi.org/10.1074/mcp.M113.030379
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author Olsson, Niclas
Carlsson, Petter
James, Peter
Hansson, Karin
Waldemarson, Sofia
Malmström, Per
Fernö, Mårten
Ryden, Lisa
Wingren, Christer
Borrebaeck, Carl A. K.
author_facet Olsson, Niclas
Carlsson, Petter
James, Peter
Hansson, Karin
Waldemarson, Sofia
Malmström, Per
Fernö, Mårten
Ryden, Lisa
Wingren, Christer
Borrebaeck, Carl A. K.
author_sort Olsson, Niclas
collection PubMed
description Tumor progression and prognosis in breast cancer patients are difficult to assess using current clinical and laboratory parameters, where a pathological grading is indicative of tumor aggressiveness. This grading is based on assessments of nuclear grade, tubule formation, and mitotic rate. We report here the first protein signatures associated with histological grades of breast cancer, determined using a novel affinity proteomics approach. We profiled 52 breast cancer tissue samples by combining nine antibodies and label-free LC-MS/MS, which generated detailed quantified proteomic maps representing 1,388 proteins. The results showed that we could define in-depth molecular portraits of histologically graded breast cancer tumors. Consequently, a 49-plex candidate tissue protein signature was defined that discriminated between histological grades 1, 2, and 3 of breast cancer tumors with high accuracy. Highly biologically relevant proteins were identified, and the differentially expressed proteins indicated further support for the current hypothesis regarding remodeling of the tumor microenvironment during tumor progression. The protein signature was corroborated using meta-analysis of transcriptional profiling data from an independent patient cohort. In addition, the potential for using the markers to estimate the likelihood of long-term metastasis-free survival was also indicated. Taken together, these molecular portraits could pave the way for improved classification and prognostication of breast cancer.
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spelling pubmed-38617112013-12-17 Grading Breast Cancer Tissues Using Molecular Portraits Olsson, Niclas Carlsson, Petter James, Peter Hansson, Karin Waldemarson, Sofia Malmström, Per Fernö, Mårten Ryden, Lisa Wingren, Christer Borrebaeck, Carl A. K. Mol Cell Proteomics Research Tumor progression and prognosis in breast cancer patients are difficult to assess using current clinical and laboratory parameters, where a pathological grading is indicative of tumor aggressiveness. This grading is based on assessments of nuclear grade, tubule formation, and mitotic rate. We report here the first protein signatures associated with histological grades of breast cancer, determined using a novel affinity proteomics approach. We profiled 52 breast cancer tissue samples by combining nine antibodies and label-free LC-MS/MS, which generated detailed quantified proteomic maps representing 1,388 proteins. The results showed that we could define in-depth molecular portraits of histologically graded breast cancer tumors. Consequently, a 49-plex candidate tissue protein signature was defined that discriminated between histological grades 1, 2, and 3 of breast cancer tumors with high accuracy. Highly biologically relevant proteins were identified, and the differentially expressed proteins indicated further support for the current hypothesis regarding remodeling of the tumor microenvironment during tumor progression. The protein signature was corroborated using meta-analysis of transcriptional profiling data from an independent patient cohort. In addition, the potential for using the markers to estimate the likelihood of long-term metastasis-free survival was also indicated. Taken together, these molecular portraits could pave the way for improved classification and prognostication of breast cancer. The American Society for Biochemistry and Molecular Biology 2013-12 2013-08-27 /pmc/articles/PMC3861711/ /pubmed/23982162 http://dx.doi.org/10.1074/mcp.M113.030379 Text en © 2013 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version full access.
spellingShingle Research
Olsson, Niclas
Carlsson, Petter
James, Peter
Hansson, Karin
Waldemarson, Sofia
Malmström, Per
Fernö, Mårten
Ryden, Lisa
Wingren, Christer
Borrebaeck, Carl A. K.
Grading Breast Cancer Tissues Using Molecular Portraits
title Grading Breast Cancer Tissues Using Molecular Portraits
title_full Grading Breast Cancer Tissues Using Molecular Portraits
title_fullStr Grading Breast Cancer Tissues Using Molecular Portraits
title_full_unstemmed Grading Breast Cancer Tissues Using Molecular Portraits
title_short Grading Breast Cancer Tissues Using Molecular Portraits
title_sort grading breast cancer tissues using molecular portraits
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3861711/
https://www.ncbi.nlm.nih.gov/pubmed/23982162
http://dx.doi.org/10.1074/mcp.M113.030379
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