Cargando…

Characterising the phenotypic evolution of circulating tumour cells during treatment

Real-time monitoring of cancer cells’ phenotypic evolution during therapy can provide vital tumour biology information for treatment management. Circulating tumour cell (CTC) analysis has emerged as a useful monitoring tool, but its routine usage is restricted by either limited multiplexing capabili...

Descripción completa

Detalles Bibliográficos
Autores principales: Tsao, Simon Chang-Hao, Wang, Jing, Wang, Yuling, Behren, Andreas, Cebon, Jonathan, Trau, Matt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902511/
https://www.ncbi.nlm.nih.gov/pubmed/29662054
http://dx.doi.org/10.1038/s41467-018-03725-8
_version_ 1783314766893154304
author Tsao, Simon Chang-Hao
Wang, Jing
Wang, Yuling
Behren, Andreas
Cebon, Jonathan
Trau, Matt
author_facet Tsao, Simon Chang-Hao
Wang, Jing
Wang, Yuling
Behren, Andreas
Cebon, Jonathan
Trau, Matt
author_sort Tsao, Simon Chang-Hao
collection PubMed
description Real-time monitoring of cancer cells’ phenotypic evolution during therapy can provide vital tumour biology information for treatment management. Circulating tumour cell (CTC) analysis has emerged as a useful monitoring tool, but its routine usage is restricted by either limited multiplexing capability or sensitivity. Here, we demonstrate the use of antibody-conjugated and Raman reporter-coated gold nanoparticles for simultaneous labelling and monitoring of multiple CTC surface markers (named as “cell signature”), without the need for isolating individual CTCs. We observe cell heterogeneity and phenotypic changes of melanoma cell lines during molecular targeted treatment. Furthermore, we follow the CTC signature changes of 10 stage-IV melanoma patients receiving immunological or molecular targeted therapies. Our technique maps the phenotypic evolution of patient CTCs sensitively and rapidly, and shows drug-resistant clones having different CTC signatures of potential clinical value. We believe our proposed method is of general interest in the CTC relevant research and translation fields.
format Online
Article
Text
id pubmed-5902511
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-59025112018-04-20 Characterising the phenotypic evolution of circulating tumour cells during treatment Tsao, Simon Chang-Hao Wang, Jing Wang, Yuling Behren, Andreas Cebon, Jonathan Trau, Matt Nat Commun Article Real-time monitoring of cancer cells’ phenotypic evolution during therapy can provide vital tumour biology information for treatment management. Circulating tumour cell (CTC) analysis has emerged as a useful monitoring tool, but its routine usage is restricted by either limited multiplexing capability or sensitivity. Here, we demonstrate the use of antibody-conjugated and Raman reporter-coated gold nanoparticles for simultaneous labelling and monitoring of multiple CTC surface markers (named as “cell signature”), without the need for isolating individual CTCs. We observe cell heterogeneity and phenotypic changes of melanoma cell lines during molecular targeted treatment. Furthermore, we follow the CTC signature changes of 10 stage-IV melanoma patients receiving immunological or molecular targeted therapies. Our technique maps the phenotypic evolution of patient CTCs sensitively and rapidly, and shows drug-resistant clones having different CTC signatures of potential clinical value. We believe our proposed method is of general interest in the CTC relevant research and translation fields. Nature Publishing Group UK 2018-04-16 /pmc/articles/PMC5902511/ /pubmed/29662054 http://dx.doi.org/10.1038/s41467-018-03725-8 Text en © The Author(s) 2018 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
Tsao, Simon Chang-Hao
Wang, Jing
Wang, Yuling
Behren, Andreas
Cebon, Jonathan
Trau, Matt
Characterising the phenotypic evolution of circulating tumour cells during treatment
title Characterising the phenotypic evolution of circulating tumour cells during treatment
title_full Characterising the phenotypic evolution of circulating tumour cells during treatment
title_fullStr Characterising the phenotypic evolution of circulating tumour cells during treatment
title_full_unstemmed Characterising the phenotypic evolution of circulating tumour cells during treatment
title_short Characterising the phenotypic evolution of circulating tumour cells during treatment
title_sort characterising the phenotypic evolution of circulating tumour cells during treatment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902511/
https://www.ncbi.nlm.nih.gov/pubmed/29662054
http://dx.doi.org/10.1038/s41467-018-03725-8
work_keys_str_mv AT tsaosimonchanghao characterisingthephenotypicevolutionofcirculatingtumourcellsduringtreatment
AT wangjing characterisingthephenotypicevolutionofcirculatingtumourcellsduringtreatment
AT wangyuling characterisingthephenotypicevolutionofcirculatingtumourcellsduringtreatment
AT behrenandreas characterisingthephenotypicevolutionofcirculatingtumourcellsduringtreatment
AT cebonjonathan characterisingthephenotypicevolutionofcirculatingtumourcellsduringtreatment
AT traumatt characterisingthephenotypicevolutionofcirculatingtumourcellsduringtreatment