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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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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. |
format | Online Article Text |
id | pubmed-4053127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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