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Sensitive capture of circulating tumour cells by functionalised graphene oxide nanosheets
The spread of cancer throughout the body is driven by circulating tumour cells (CTCs)(1). These cells detach from the primary tumour and move from the blood stream to a new site of subsequent tumour growth. They also carry information about the primary tumour and have the potential to be valuable bi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017624/ https://www.ncbi.nlm.nih.gov/pubmed/24077027 http://dx.doi.org/10.1038/nnano.2013.194 |
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author | Yoon, Hyeun Joong Kim, Tae Hyun Zhang, Zhuo Azizi, Ebrahim Pham, Trinh M. Paoletti, Costanza Lin, Jules Ramnath, Nithya Wicha, Max S. Hayes, Daniel F. Simeone, Diane M. Nagrath, Sunitha |
author_facet | Yoon, Hyeun Joong Kim, Tae Hyun Zhang, Zhuo Azizi, Ebrahim Pham, Trinh M. Paoletti, Costanza Lin, Jules Ramnath, Nithya Wicha, Max S. Hayes, Daniel F. Simeone, Diane M. Nagrath, Sunitha |
author_sort | Yoon, Hyeun Joong |
collection | PubMed |
description | The spread of cancer throughout the body is driven by circulating tumour cells (CTCs)(1). These cells detach from the primary tumour and move from the blood stream to a new site of subsequent tumour growth. They also carry information about the primary tumour and have the potential to be valuable biomarkers for disease diagnosis and progression, and for the molecular characterization of certain biological properties of the tumour. However, the limited sensitivity and specificity of current methods to measure and study these cells in patient blood samples prevent the realization of their full clinical potential. The use of microfluidic devices is a promising method for isolating CTCs(2, 3); however, the devices are reliant on three-dimensional structures, which limit further characterization and expansion of cells on the chip. Here we demonstrate an effective approach to isolate CTCs from blood samples of pancreatic, breast and lung cancer patients, by using functionalised graphene oxide nanosheets on a patterned gold surface. CTCs were captured with high sensitivity at low concentration of target cells (73% ± 32.4 at 3–5 cells/mL blood). |
format | Online Article Text |
id | pubmed-4017624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-40176242014-05-12 Sensitive capture of circulating tumour cells by functionalised graphene oxide nanosheets Yoon, Hyeun Joong Kim, Tae Hyun Zhang, Zhuo Azizi, Ebrahim Pham, Trinh M. Paoletti, Costanza Lin, Jules Ramnath, Nithya Wicha, Max S. Hayes, Daniel F. Simeone, Diane M. Nagrath, Sunitha Nat Nanotechnol Article The spread of cancer throughout the body is driven by circulating tumour cells (CTCs)(1). These cells detach from the primary tumour and move from the blood stream to a new site of subsequent tumour growth. They also carry information about the primary tumour and have the potential to be valuable biomarkers for disease diagnosis and progression, and for the molecular characterization of certain biological properties of the tumour. However, the limited sensitivity and specificity of current methods to measure and study these cells in patient blood samples prevent the realization of their full clinical potential. The use of microfluidic devices is a promising method for isolating CTCs(2, 3); however, the devices are reliant on three-dimensional structures, which limit further characterization and expansion of cells on the chip. Here we demonstrate an effective approach to isolate CTCs from blood samples of pancreatic, breast and lung cancer patients, by using functionalised graphene oxide nanosheets on a patterned gold surface. CTCs were captured with high sensitivity at low concentration of target cells (73% ± 32.4 at 3–5 cells/mL blood). 2013-09-29 2013-10 /pmc/articles/PMC4017624/ /pubmed/24077027 http://dx.doi.org/10.1038/nnano.2013.194 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Yoon, Hyeun Joong Kim, Tae Hyun Zhang, Zhuo Azizi, Ebrahim Pham, Trinh M. Paoletti, Costanza Lin, Jules Ramnath, Nithya Wicha, Max S. Hayes, Daniel F. Simeone, Diane M. Nagrath, Sunitha Sensitive capture of circulating tumour cells by functionalised graphene oxide nanosheets |
title | Sensitive capture of circulating tumour cells by functionalised graphene oxide nanosheets |
title_full | Sensitive capture of circulating tumour cells by functionalised graphene oxide nanosheets |
title_fullStr | Sensitive capture of circulating tumour cells by functionalised graphene oxide nanosheets |
title_full_unstemmed | Sensitive capture of circulating tumour cells by functionalised graphene oxide nanosheets |
title_short | Sensitive capture of circulating tumour cells by functionalised graphene oxide nanosheets |
title_sort | sensitive capture of circulating tumour cells by functionalised graphene oxide nanosheets |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017624/ https://www.ncbi.nlm.nih.gov/pubmed/24077027 http://dx.doi.org/10.1038/nnano.2013.194 |
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