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Diagnostic technologies for circulating tumour cells and exosomes

Circulating tumour cells (CTCs) and exosomes are promising circulating biomarkers. They exist in easily accessible blood and carry large diversity of molecular information. As such, they can be easily and repeatedly obtained for minimally invasive cancer diagnosis and monitoring. Because of their in...

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Detalles Bibliográficos
Autores principales: Shao, Huilin, Chung, Jaehoon, Issadore, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741183/
https://www.ncbi.nlm.nih.gov/pubmed/26604322
http://dx.doi.org/10.1042/BSR20150180
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author Shao, Huilin
Chung, Jaehoon
Issadore, David
author_facet Shao, Huilin
Chung, Jaehoon
Issadore, David
author_sort Shao, Huilin
collection PubMed
description Circulating tumour cells (CTCs) and exosomes are promising circulating biomarkers. They exist in easily accessible blood and carry large diversity of molecular information. As such, they can be easily and repeatedly obtained for minimally invasive cancer diagnosis and monitoring. Because of their intrinsic differences in counts, size and molecular contents, CTCs and exosomes pose unique sets of technical challenges for clinical translation–CTCs are rare whereas exosomes are small. Novel technologies are underway to overcome these specific challenges to fully harness the clinical potential of these circulating biomarkers. Herein, we will overview the characteristics of CTCs and exosomes as valuable circulating biomarkers and their associated technical challenges for clinical adaptation. Specifically, we will describe emerging technologies that have been developed to address these technical obstacles and the unique clinical opportunities enabled by technological innovations.
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spelling pubmed-47411832016-02-22 Diagnostic technologies for circulating tumour cells and exosomes Shao, Huilin Chung, Jaehoon Issadore, David Biosci Rep Review Articles Circulating tumour cells (CTCs) and exosomes are promising circulating biomarkers. They exist in easily accessible blood and carry large diversity of molecular information. As such, they can be easily and repeatedly obtained for minimally invasive cancer diagnosis and monitoring. Because of their intrinsic differences in counts, size and molecular contents, CTCs and exosomes pose unique sets of technical challenges for clinical translation–CTCs are rare whereas exosomes are small. Novel technologies are underway to overcome these specific challenges to fully harness the clinical potential of these circulating biomarkers. Herein, we will overview the characteristics of CTCs and exosomes as valuable circulating biomarkers and their associated technical challenges for clinical adaptation. Specifically, we will describe emerging technologies that have been developed to address these technical obstacles and the unique clinical opportunities enabled by technological innovations. Portland Press Ltd. 2016-02-03 /pmc/articles/PMC4741183/ /pubmed/26604322 http://dx.doi.org/10.1042/BSR20150180 Text en © 2016 Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article published by Portland Press Limited and distributed under the Creative Commons Attribution Licence 3.0 (http://creativecommons.org/licenses/by/3.0/) .
spellingShingle Review Articles
Shao, Huilin
Chung, Jaehoon
Issadore, David
Diagnostic technologies for circulating tumour cells and exosomes
title Diagnostic technologies for circulating tumour cells and exosomes
title_full Diagnostic technologies for circulating tumour cells and exosomes
title_fullStr Diagnostic technologies for circulating tumour cells and exosomes
title_full_unstemmed Diagnostic technologies for circulating tumour cells and exosomes
title_short Diagnostic technologies for circulating tumour cells and exosomes
title_sort diagnostic technologies for circulating tumour cells and exosomes
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741183/
https://www.ncbi.nlm.nih.gov/pubmed/26604322
http://dx.doi.org/10.1042/BSR20150180
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