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Leveraging ectopic Hsp90 expression to assay the presence of tumor cells and aggressive tumor phenotypes in breast specimens
Hsp90 has been studied extensively as a therapeutic target in breast cancer in pre-clinical and clinical trials, demonstrating a variety of roles in metastatic progression. The evidence to date suggests a compelling opportunity to leverage attributes of Hsp90 expression beyond therapeutics with pote...
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/PMC5727497/ https://www.ncbi.nlm.nih.gov/pubmed/29235516 http://dx.doi.org/10.1038/s41598-017-17832-x |
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author | Crouch, Brian Murphy, Helen Belonwu, Stella Martinez, Amy Gallagher, Jennifer Hall, Allison Soo, Mary Scott Lee, Marianne Hughes, Philip Haystead, Timothy Ramanujam, Nirmala |
author_facet | Crouch, Brian Murphy, Helen Belonwu, Stella Martinez, Amy Gallagher, Jennifer Hall, Allison Soo, Mary Scott Lee, Marianne Hughes, Philip Haystead, Timothy Ramanujam, Nirmala |
author_sort | Crouch, Brian |
collection | PubMed |
description | Hsp90 has been studied extensively as a therapeutic target in breast cancer in pre-clinical and clinical trials, demonstrating a variety of roles in metastatic progression. The evidence to date suggests a compelling opportunity to leverage attributes of Hsp90 expression beyond therapeutics with potential applications in breast cancer diagnosis, prognosis, and recurrence risk assessment. In this study, we developed a completely non-destructive strategy using HS-27, a fluorescently-tethered Hsp90 inhibitor, to assay Hsp90 expression on intact tissue specimens with comparable contrast to in vivo administration routes, and demonstrate the feasibility of our approach in breast cancer patients. In addition to Hsp90 inhibition being most effective in glycolytic tumors, we found ectopic Hsp90 expression to be highest in glycolytic tumors reinforcing its role as an indicator of aggressive disease. This work sets the stage for immediately using Hsp90 to improve outcomes for breast cancer patients without affecting traditional care pathways. |
format | Online Article Text |
id | pubmed-5727497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57274972017-12-18 Leveraging ectopic Hsp90 expression to assay the presence of tumor cells and aggressive tumor phenotypes in breast specimens Crouch, Brian Murphy, Helen Belonwu, Stella Martinez, Amy Gallagher, Jennifer Hall, Allison Soo, Mary Scott Lee, Marianne Hughes, Philip Haystead, Timothy Ramanujam, Nirmala Sci Rep Article Hsp90 has been studied extensively as a therapeutic target in breast cancer in pre-clinical and clinical trials, demonstrating a variety of roles in metastatic progression. The evidence to date suggests a compelling opportunity to leverage attributes of Hsp90 expression beyond therapeutics with potential applications in breast cancer diagnosis, prognosis, and recurrence risk assessment. In this study, we developed a completely non-destructive strategy using HS-27, a fluorescently-tethered Hsp90 inhibitor, to assay Hsp90 expression on intact tissue specimens with comparable contrast to in vivo administration routes, and demonstrate the feasibility of our approach in breast cancer patients. In addition to Hsp90 inhibition being most effective in glycolytic tumors, we found ectopic Hsp90 expression to be highest in glycolytic tumors reinforcing its role as an indicator of aggressive disease. This work sets the stage for immediately using Hsp90 to improve outcomes for breast cancer patients without affecting traditional care pathways. Nature Publishing Group UK 2017-12-13 /pmc/articles/PMC5727497/ /pubmed/29235516 http://dx.doi.org/10.1038/s41598-017-17832-x 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 Crouch, Brian Murphy, Helen Belonwu, Stella Martinez, Amy Gallagher, Jennifer Hall, Allison Soo, Mary Scott Lee, Marianne Hughes, Philip Haystead, Timothy Ramanujam, Nirmala Leveraging ectopic Hsp90 expression to assay the presence of tumor cells and aggressive tumor phenotypes in breast specimens |
title | Leveraging ectopic Hsp90 expression to assay the presence of tumor cells and aggressive tumor phenotypes in breast specimens |
title_full | Leveraging ectopic Hsp90 expression to assay the presence of tumor cells and aggressive tumor phenotypes in breast specimens |
title_fullStr | Leveraging ectopic Hsp90 expression to assay the presence of tumor cells and aggressive tumor phenotypes in breast specimens |
title_full_unstemmed | Leveraging ectopic Hsp90 expression to assay the presence of tumor cells and aggressive tumor phenotypes in breast specimens |
title_short | Leveraging ectopic Hsp90 expression to assay the presence of tumor cells and aggressive tumor phenotypes in breast specimens |
title_sort | leveraging ectopic hsp90 expression to assay the presence of tumor cells and aggressive tumor phenotypes in breast specimens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727497/ https://www.ncbi.nlm.nih.gov/pubmed/29235516 http://dx.doi.org/10.1038/s41598-017-17832-x |
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