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Molecular characterization of breast cancer CTCs associated with brain metastasis
The enumeration of EpCAM-positive circulating tumor cells (CTCs) has allowed estimation of overall metastatic burden in breast cancer patients. However, a thorough understanding of CTCs associated with breast cancer brain metastasis (BCBM) is necessary for early identification and evaluation of trea...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543046/ https://www.ncbi.nlm.nih.gov/pubmed/28775303 http://dx.doi.org/10.1038/s41467-017-00196-1 |
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author | Boral, Debasish Vishnoi, Monika Liu, Haowen N. Yin, Wei Sprouse, Marc L. Scamardo, Antonio Hong, David S. Tan, Tuan Z. Thiery, Jean P. Chang, Jenny C. Marchetti, Dario |
author_facet | Boral, Debasish Vishnoi, Monika Liu, Haowen N. Yin, Wei Sprouse, Marc L. Scamardo, Antonio Hong, David S. Tan, Tuan Z. Thiery, Jean P. Chang, Jenny C. Marchetti, Dario |
author_sort | Boral, Debasish |
collection | PubMed |
description | The enumeration of EpCAM-positive circulating tumor cells (CTCs) has allowed estimation of overall metastatic burden in breast cancer patients. However, a thorough understanding of CTCs associated with breast cancer brain metastasis (BCBM) is necessary for early identification and evaluation of treatment response to BCBM. Here we report that BCBM CTCs is enriched in a distinct sub-population of cells identifiable by their biomarker expression and mutational content. Deriving from a comprehensive analysis of CTC transcriptomes, we discovered a unique “circulating tumor cell gene signature” that is distinct from primary breast cancer tissues. Further dissection of the circulating tumor cell gene signature identified signaling pathways associated with BCBM CTCs that may have roles in potentiating BCBM. This study proposes CTC biomarkers and signaling pathways implicated in BCBM that may be used either as a screening tool for brain micro-metastasis detection or for making rational treatment decisions and monitoring therapeutic response in patients with BCBM. |
format | Online Article Text |
id | pubmed-5543046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55430462017-08-09 Molecular characterization of breast cancer CTCs associated with brain metastasis Boral, Debasish Vishnoi, Monika Liu, Haowen N. Yin, Wei Sprouse, Marc L. Scamardo, Antonio Hong, David S. Tan, Tuan Z. Thiery, Jean P. Chang, Jenny C. Marchetti, Dario Nat Commun Article The enumeration of EpCAM-positive circulating tumor cells (CTCs) has allowed estimation of overall metastatic burden in breast cancer patients. However, a thorough understanding of CTCs associated with breast cancer brain metastasis (BCBM) is necessary for early identification and evaluation of treatment response to BCBM. Here we report that BCBM CTCs is enriched in a distinct sub-population of cells identifiable by their biomarker expression and mutational content. Deriving from a comprehensive analysis of CTC transcriptomes, we discovered a unique “circulating tumor cell gene signature” that is distinct from primary breast cancer tissues. Further dissection of the circulating tumor cell gene signature identified signaling pathways associated with BCBM CTCs that may have roles in potentiating BCBM. This study proposes CTC biomarkers and signaling pathways implicated in BCBM that may be used either as a screening tool for brain micro-metastasis detection or for making rational treatment decisions and monitoring therapeutic response in patients with BCBM. Nature Publishing Group UK 2017-08-04 /pmc/articles/PMC5543046/ /pubmed/28775303 http://dx.doi.org/10.1038/s41467-017-00196-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Boral, Debasish Vishnoi, Monika Liu, Haowen N. Yin, Wei Sprouse, Marc L. Scamardo, Antonio Hong, David S. Tan, Tuan Z. Thiery, Jean P. Chang, Jenny C. Marchetti, Dario Molecular characterization of breast cancer CTCs associated with brain metastasis |
title | Molecular characterization of breast cancer CTCs associated with brain metastasis |
title_full | Molecular characterization of breast cancer CTCs associated with brain metastasis |
title_fullStr | Molecular characterization of breast cancer CTCs associated with brain metastasis |
title_full_unstemmed | Molecular characterization of breast cancer CTCs associated with brain metastasis |
title_short | Molecular characterization of breast cancer CTCs associated with brain metastasis |
title_sort | molecular characterization of breast cancer ctcs associated with brain metastasis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5543046/ https://www.ncbi.nlm.nih.gov/pubmed/28775303 http://dx.doi.org/10.1038/s41467-017-00196-1 |
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