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Biostable ssDNA Aptamers Specific for Hodgkin Lymphoma
As a “chemical antibody”, oligonucleotide aptamers can specifically bind to their target molecules. However, clinical potential of aptamers in disease diagnosis is not yet fully explored. Using a tumor cell-based selection protocol, we developed single-stranded DNA aptamers for Hodgkin lymphoma (HL)...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871109/ https://www.ncbi.nlm.nih.gov/pubmed/24233078 http://dx.doi.org/10.3390/s131114543 |
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author | Parekh, Parag Kamble, Sanchit Zhao, Nianxi Zeng, Zihua Wen, Jianguo Yuan, Bin Zu, Youli |
author_facet | Parekh, Parag Kamble, Sanchit Zhao, Nianxi Zeng, Zihua Wen, Jianguo Yuan, Bin Zu, Youli |
author_sort | Parekh, Parag |
collection | PubMed |
description | As a “chemical antibody”, oligonucleotide aptamers can specifically bind to their target molecules. However, clinical potential of aptamers in disease diagnosis is not yet fully explored. Using a tumor cell-based selection protocol, we developed single-stranded DNA aptamers for Hodgkin lymphoma (HL) tumor cells. The aptamers specifically bound to HL cells with a high affinity, reaching maximal cell binding at 10 nM final concentration. Importantly, the aptamers were able to selectively detect HL cells and did not react to other tumor or blood cells in mixed samples, indicating that the aptamers can be used as a specific probe for in vitro analysis of HL cells. Moreover, due to the inherent properties of DNA, the aptamers were stable in human serum, suggesting potential for in vivo detection of HL tumor cells. |
format | Online Article Text |
id | pubmed-3871109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-38711092013-12-26 Biostable ssDNA Aptamers Specific for Hodgkin Lymphoma Parekh, Parag Kamble, Sanchit Zhao, Nianxi Zeng, Zihua Wen, Jianguo Yuan, Bin Zu, Youli Sensors (Basel) Article As a “chemical antibody”, oligonucleotide aptamers can specifically bind to their target molecules. However, clinical potential of aptamers in disease diagnosis is not yet fully explored. Using a tumor cell-based selection protocol, we developed single-stranded DNA aptamers for Hodgkin lymphoma (HL) tumor cells. The aptamers specifically bound to HL cells with a high affinity, reaching maximal cell binding at 10 nM final concentration. Importantly, the aptamers were able to selectively detect HL cells and did not react to other tumor or blood cells in mixed samples, indicating that the aptamers can be used as a specific probe for in vitro analysis of HL cells. Moreover, due to the inherent properties of DNA, the aptamers were stable in human serum, suggesting potential for in vivo detection of HL tumor cells. Molecular Diversity Preservation International (MDPI) 2013-10-25 /pmc/articles/PMC3871109/ /pubmed/24233078 http://dx.doi.org/10.3390/s131114543 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Parekh, Parag Kamble, Sanchit Zhao, Nianxi Zeng, Zihua Wen, Jianguo Yuan, Bin Zu, Youli Biostable ssDNA Aptamers Specific for Hodgkin Lymphoma |
title | Biostable ssDNA Aptamers Specific for Hodgkin Lymphoma |
title_full | Biostable ssDNA Aptamers Specific for Hodgkin Lymphoma |
title_fullStr | Biostable ssDNA Aptamers Specific for Hodgkin Lymphoma |
title_full_unstemmed | Biostable ssDNA Aptamers Specific for Hodgkin Lymphoma |
title_short | Biostable ssDNA Aptamers Specific for Hodgkin Lymphoma |
title_sort | biostable ssdna aptamers specific for hodgkin lymphoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871109/ https://www.ncbi.nlm.nih.gov/pubmed/24233078 http://dx.doi.org/10.3390/s131114543 |
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