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Clinical application of high-throughput genomic technologies for treatment selection in breast cancer

Large-scale collaborative initiatives using next-generation DNA sequencing and other high-throughput technologies have begun to characterize the genomic landscape of breast cancer. These landmark studies have identified infrequent driver mutations that are potential targets for therapeutic intervent...

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Detalles Bibliográficos
Autores principales: Hansen, Aaron R, Bedard, Philippe L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979162/
https://www.ncbi.nlm.nih.gov/pubmed/24135425
http://dx.doi.org/10.1186/bcr3558
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author Hansen, Aaron R
Bedard, Philippe L
author_facet Hansen, Aaron R
Bedard, Philippe L
author_sort Hansen, Aaron R
collection PubMed
description Large-scale collaborative initiatives using next-generation DNA sequencing and other high-throughput technologies have begun to characterize the genomic landscape of breast cancer. These landmark studies have identified infrequent driver mutations that are potential targets for therapeutic intervention with approved or investigational drug treatments, among other important discoveries. Recently, many institutions have launched molecular screening programs that apply high-throughput genomic technologies to patients with advanced solid malignancies, including breast cancer, to inform clinical decision-making. This article provides an overview of the recent molecular insights in breast cancer, including potentially actionable somatic alterations, the technological platforms currently available in a clinical diagnostics setting to detect these alterations, and ongoing institutional or regional molecular screening programs in advanced breast cancer.
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spelling pubmed-39791622014-04-18 Clinical application of high-throughput genomic technologies for treatment selection in breast cancer Hansen, Aaron R Bedard, Philippe L Breast Cancer Res Review Large-scale collaborative initiatives using next-generation DNA sequencing and other high-throughput technologies have begun to characterize the genomic landscape of breast cancer. These landmark studies have identified infrequent driver mutations that are potential targets for therapeutic intervention with approved or investigational drug treatments, among other important discoveries. Recently, many institutions have launched molecular screening programs that apply high-throughput genomic technologies to patients with advanced solid malignancies, including breast cancer, to inform clinical decision-making. This article provides an overview of the recent molecular insights in breast cancer, including potentially actionable somatic alterations, the technological platforms currently available in a clinical diagnostics setting to detect these alterations, and ongoing institutional or regional molecular screening programs in advanced breast cancer. BioMed Central 2013 2013-10-18 /pmc/articles/PMC3979162/ /pubmed/24135425 http://dx.doi.org/10.1186/bcr3558 Text en Copyright © 2013 BioMed Central Ltd.
spellingShingle Review
Hansen, Aaron R
Bedard, Philippe L
Clinical application of high-throughput genomic technologies for treatment selection in breast cancer
title Clinical application of high-throughput genomic technologies for treatment selection in breast cancer
title_full Clinical application of high-throughput genomic technologies for treatment selection in breast cancer
title_fullStr Clinical application of high-throughput genomic technologies for treatment selection in breast cancer
title_full_unstemmed Clinical application of high-throughput genomic technologies for treatment selection in breast cancer
title_short Clinical application of high-throughput genomic technologies for treatment selection in breast cancer
title_sort clinical application of high-throughput genomic technologies for treatment selection in breast cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979162/
https://www.ncbi.nlm.nih.gov/pubmed/24135425
http://dx.doi.org/10.1186/bcr3558
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