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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
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.
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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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