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Heterogeneity of miR-10b expression in circulating tumor cells
Circulating tumor cells (CTCs) in the blood of cancer patients are recognized as important potential targets for future anticancer therapies. As mediators of metastatic spread, CTCs are also promising to be used as ‘liquid biopsy’ to aid clinical decision-making. Recent work has revealed potentially...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629160/ https://www.ncbi.nlm.nih.gov/pubmed/26522916 http://dx.doi.org/10.1038/srep15980 |
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author | Gasch, Christin Plummer, Prue N. Jovanovic, Lidija McInnes, Linda M. Wescott, David Saunders, Christobel M. Schneeweiss, Andreas Wallwiener, Markus Nelson, Colleen Spring, Kevin J. Riethdorf, Sabine Thompson, Erik W. Pantel, Klaus Mellick, Albert S. |
author_facet | Gasch, Christin Plummer, Prue N. Jovanovic, Lidija McInnes, Linda M. Wescott, David Saunders, Christobel M. Schneeweiss, Andreas Wallwiener, Markus Nelson, Colleen Spring, Kevin J. Riethdorf, Sabine Thompson, Erik W. Pantel, Klaus Mellick, Albert S. |
author_sort | Gasch, Christin |
collection | PubMed |
description | Circulating tumor cells (CTCs) in the blood of cancer patients are recognized as important potential targets for future anticancer therapies. As mediators of metastatic spread, CTCs are also promising to be used as ‘liquid biopsy’ to aid clinical decision-making. Recent work has revealed potentially important genotypic and phenotypic heterogeneity within CTC populations, even within the same patient. MicroRNAs (miRNAs) are key regulators of gene expression and have emerged as potentially important diagnostic markers and targets for anti-cancer therapy. Here, we describe a robust in situ hybridization (ISH) protocol, incorporating the CellSearch(®) CTC detection system, enabling clinical investigation of important miRNAs, such as miR-10b on a cell by cell basis. We also use this method to demonstrate heterogeneity of such as miR-10b on a cell-by-cell basis. We also use this method to demonstrate heterogeneity of miR-10b in individual CTCs from breast, prostate and colorectal cancer patients. |
format | Online Article Text |
id | pubmed-4629160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46291602015-11-05 Heterogeneity of miR-10b expression in circulating tumor cells Gasch, Christin Plummer, Prue N. Jovanovic, Lidija McInnes, Linda M. Wescott, David Saunders, Christobel M. Schneeweiss, Andreas Wallwiener, Markus Nelson, Colleen Spring, Kevin J. Riethdorf, Sabine Thompson, Erik W. Pantel, Klaus Mellick, Albert S. Sci Rep Article Circulating tumor cells (CTCs) in the blood of cancer patients are recognized as important potential targets for future anticancer therapies. As mediators of metastatic spread, CTCs are also promising to be used as ‘liquid biopsy’ to aid clinical decision-making. Recent work has revealed potentially important genotypic and phenotypic heterogeneity within CTC populations, even within the same patient. MicroRNAs (miRNAs) are key regulators of gene expression and have emerged as potentially important diagnostic markers and targets for anti-cancer therapy. Here, we describe a robust in situ hybridization (ISH) protocol, incorporating the CellSearch(®) CTC detection system, enabling clinical investigation of important miRNAs, such as miR-10b on a cell by cell basis. We also use this method to demonstrate heterogeneity of such as miR-10b on a cell-by-cell basis. We also use this method to demonstrate heterogeneity of miR-10b in individual CTCs from breast, prostate and colorectal cancer patients. Nature Publishing Group 2015-11-02 /pmc/articles/PMC4629160/ /pubmed/26522916 http://dx.doi.org/10.1038/srep15980 Text en Copyright © 2015, Macmillan Publishers Limited 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 Gasch, Christin Plummer, Prue N. Jovanovic, Lidija McInnes, Linda M. Wescott, David Saunders, Christobel M. Schneeweiss, Andreas Wallwiener, Markus Nelson, Colleen Spring, Kevin J. Riethdorf, Sabine Thompson, Erik W. Pantel, Klaus Mellick, Albert S. Heterogeneity of miR-10b expression in circulating tumor cells |
title | Heterogeneity of miR-10b expression in circulating tumor cells |
title_full | Heterogeneity of miR-10b expression in circulating tumor cells |
title_fullStr | Heterogeneity of miR-10b expression in circulating tumor cells |
title_full_unstemmed | Heterogeneity of miR-10b expression in circulating tumor cells |
title_short | Heterogeneity of miR-10b expression in circulating tumor cells |
title_sort | heterogeneity of mir-10b expression in circulating tumor cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4629160/ https://www.ncbi.nlm.nih.gov/pubmed/26522916 http://dx.doi.org/10.1038/srep15980 |
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