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A 3q gene signature associated with triple negative breast cancer organ specific metastasis and response to neoadjuvant chemotherapy
Triple negative breast cancers (TNBC) are aggressive tumors, with high rates of metastatic spread and targeted therapies are critically needed. We aimed to assess the prognostic and predictive value of a 3q 19-gene signature identified previously from lung cancer in a collection of 4,801 breast tumo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384279/ https://www.ncbi.nlm.nih.gov/pubmed/28387221 http://dx.doi.org/10.1038/srep45828 |
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author | Qian, Jun Chen, Heidi Ji, Xiangming Eisenberg, Rosana Chakravarthy, A. Bapsi Mayer, Ingrid A. Massion, Pierre P. |
author_facet | Qian, Jun Chen, Heidi Ji, Xiangming Eisenberg, Rosana Chakravarthy, A. Bapsi Mayer, Ingrid A. Massion, Pierre P. |
author_sort | Qian, Jun |
collection | PubMed |
description | Triple negative breast cancers (TNBC) are aggressive tumors, with high rates of metastatic spread and targeted therapies are critically needed. We aimed to assess the prognostic and predictive value of a 3q 19-gene signature identified previously from lung cancer in a collection of 4,801 breast tumor gene expression data. The 3q gene signature had a strong association with features of aggressiveness such as high grade, hormone receptor negativity, presence of a basal-like or TNBC phenotype and reduced distant metastasis free survival. The 3q gene signature was strongly associated with lung metastasis only in TNBC (P < 0.0001, Hazard ratio (HR) 1.44, 95% confidence interval (CI), 1.31–1.60), significantly associated with brain but not bone metastasis regardless of TNBC status. The association of one 3q driver gene FXR1 with distant metastasis in TNBC (P = 0.01) was further validated by immunohistochemistry. In addition, the 3q gene signature was associated with better response to neoadjuvant chemotherapy in TNBC (P < 0.0001) but not in non-TNBC patients. Our study suggests that the 3q gene signature is a novel prognostic marker for lung and/or brain metastasis and a predictive marker for the response to neoadjuvant chemotherapy in TNBC, implying a potential role for 3q genes in the mechanism of organ-specific metastasis. |
format | Online Article Text |
id | pubmed-5384279 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53842792017-04-11 A 3q gene signature associated with triple negative breast cancer organ specific metastasis and response to neoadjuvant chemotherapy Qian, Jun Chen, Heidi Ji, Xiangming Eisenberg, Rosana Chakravarthy, A. Bapsi Mayer, Ingrid A. Massion, Pierre P. Sci Rep Article Triple negative breast cancers (TNBC) are aggressive tumors, with high rates of metastatic spread and targeted therapies are critically needed. We aimed to assess the prognostic and predictive value of a 3q 19-gene signature identified previously from lung cancer in a collection of 4,801 breast tumor gene expression data. The 3q gene signature had a strong association with features of aggressiveness such as high grade, hormone receptor negativity, presence of a basal-like or TNBC phenotype and reduced distant metastasis free survival. The 3q gene signature was strongly associated with lung metastasis only in TNBC (P < 0.0001, Hazard ratio (HR) 1.44, 95% confidence interval (CI), 1.31–1.60), significantly associated with brain but not bone metastasis regardless of TNBC status. The association of one 3q driver gene FXR1 with distant metastasis in TNBC (P = 0.01) was further validated by immunohistochemistry. In addition, the 3q gene signature was associated with better response to neoadjuvant chemotherapy in TNBC (P < 0.0001) but not in non-TNBC patients. Our study suggests that the 3q gene signature is a novel prognostic marker for lung and/or brain metastasis and a predictive marker for the response to neoadjuvant chemotherapy in TNBC, implying a potential role for 3q genes in the mechanism of organ-specific metastasis. Nature Publishing Group 2017-04-07 /pmc/articles/PMC5384279/ /pubmed/28387221 http://dx.doi.org/10.1038/srep45828 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Qian, Jun Chen, Heidi Ji, Xiangming Eisenberg, Rosana Chakravarthy, A. Bapsi Mayer, Ingrid A. Massion, Pierre P. A 3q gene signature associated with triple negative breast cancer organ specific metastasis and response to neoadjuvant chemotherapy |
title | A 3q gene signature associated with triple negative breast cancer organ specific metastasis and response to neoadjuvant chemotherapy |
title_full | A 3q gene signature associated with triple negative breast cancer organ specific metastasis and response to neoadjuvant chemotherapy |
title_fullStr | A 3q gene signature associated with triple negative breast cancer organ specific metastasis and response to neoadjuvant chemotherapy |
title_full_unstemmed | A 3q gene signature associated with triple negative breast cancer organ specific metastasis and response to neoadjuvant chemotherapy |
title_short | A 3q gene signature associated with triple negative breast cancer organ specific metastasis and response to neoadjuvant chemotherapy |
title_sort | 3q gene signature associated with triple negative breast cancer organ specific metastasis and response to neoadjuvant chemotherapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384279/ https://www.ncbi.nlm.nih.gov/pubmed/28387221 http://dx.doi.org/10.1038/srep45828 |
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