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FGFR1 amplification and the progression of non-invasive to invasive breast cancer

The incidence of invasive breast cancer (IBC) can be dramatically reduced by improving our abilities to detect and treat ductal carcinoma in situ (DCIS). Progress will be based on a detailed understanding of molecular mechanisms responsible for tumor progression. An interesting study by Jang and col...

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Autores principales: Gru, Alejandro A, Allred, D Craig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053127/
https://www.ncbi.nlm.nih.gov/pubmed/23151501
http://dx.doi.org/10.1186/bcr3340
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author Gru, Alejandro A
Allred, D Craig
author_facet Gru, Alejandro A
Allred, D Craig
author_sort Gru, Alejandro A
collection PubMed
description The incidence of invasive breast cancer (IBC) can be dramatically reduced by improving our abilities to detect and treat ductal carcinoma in situ (DCIS). Progress will be based on a detailed understanding of molecular mechanisms responsible for tumor progression. An interesting study by Jang and colleagues evaluated and compared the frequency of amplification of four oncogenes (HER2, c-MYC, CCND1 and FGFR1) in large cohorts of pure DCIS, in the DCIS component of IBC, and in corresponding IBC. Of particular interest, they found a twofold increase in FGFR1 amplification in IBC versus pure DCIS, and significantly reduced disease-free survival in amplified versus unamplified IBC - leading the authors to conclude that FGFR1 plays an important role in the development and progression of IBC. These observations indeed provide hints that FGFR1 is important in this setting, although the issue is very complex and far from resolved.
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spelling pubmed-40531272014-06-12 FGFR1 amplification and the progression of non-invasive to invasive breast cancer Gru, Alejandro A Allred, D Craig Breast Cancer Res Editorial The incidence of invasive breast cancer (IBC) can be dramatically reduced by improving our abilities to detect and treat ductal carcinoma in situ (DCIS). Progress will be based on a detailed understanding of molecular mechanisms responsible for tumor progression. An interesting study by Jang and colleagues evaluated and compared the frequency of amplification of four oncogenes (HER2, c-MYC, CCND1 and FGFR1) in large cohorts of pure DCIS, in the DCIS component of IBC, and in corresponding IBC. Of particular interest, they found a twofold increase in FGFR1 amplification in IBC versus pure DCIS, and significantly reduced disease-free survival in amplified versus unamplified IBC - leading the authors to conclude that FGFR1 plays an important role in the development and progression of IBC. These observations indeed provide hints that FGFR1 is important in this setting, although the issue is very complex and far from resolved. BioMed Central 2012 2012-11-14 /pmc/articles/PMC4053127/ /pubmed/23151501 http://dx.doi.org/10.1186/bcr3340 Text en Copyright © 2012 BioMed Central Ltd
spellingShingle Editorial
Gru, Alejandro A
Allred, D Craig
FGFR1 amplification and the progression of non-invasive to invasive breast cancer
title FGFR1 amplification and the progression of non-invasive to invasive breast cancer
title_full FGFR1 amplification and the progression of non-invasive to invasive breast cancer
title_fullStr FGFR1 amplification and the progression of non-invasive to invasive breast cancer
title_full_unstemmed FGFR1 amplification and the progression of non-invasive to invasive breast cancer
title_short FGFR1 amplification and the progression of non-invasive to invasive breast cancer
title_sort fgfr1 amplification and the progression of non-invasive to invasive breast cancer
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053127/
https://www.ncbi.nlm.nih.gov/pubmed/23151501
http://dx.doi.org/10.1186/bcr3340
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