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An ‘activatable’ aptamer-based fluorescence probe for the detection of HepG2 cells

It is significant to develop a probe with sensitivity and specificity for the detection of cancer cells. The present study aimed to develop an ‘activatable’ aptamer-based fluorescence probe (AAFP) to detect cancer cells and frozen cancer tissue. This AAFP consisted of two fragments: aptamer TLS11a t...

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Autores principales: Lai, Zongqiang, Tan, Juntao, Wan, Ruirong, Tan, Jie, Zhang, Zhenghua, Hu, Zixi, Li, Jieping, Yang, Wei, Wang, Yiwei, Jiang, Yafeng, He, Jian, Yang, Nuo, Lu, Xiaoling, Zhao, Yongxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428880/
https://www.ncbi.nlm.nih.gov/pubmed/28339076
http://dx.doi.org/10.3892/or.2017.5527
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author Lai, Zongqiang
Tan, Juntao
Wan, Ruirong
Tan, Jie
Zhang, Zhenghua
Hu, Zixi
Li, Jieping
Yang, Wei
Wang, Yiwei
Jiang, Yafeng
He, Jian
Yang, Nuo
Lu, Xiaoling
Zhao, Yongxiang
author_facet Lai, Zongqiang
Tan, Juntao
Wan, Ruirong
Tan, Jie
Zhang, Zhenghua
Hu, Zixi
Li, Jieping
Yang, Wei
Wang, Yiwei
Jiang, Yafeng
He, Jian
Yang, Nuo
Lu, Xiaoling
Zhao, Yongxiang
author_sort Lai, Zongqiang
collection PubMed
description It is significant to develop a probe with sensitivity and specificity for the detection of cancer cells. The present study aimed to develop an ‘activatable’ aptamer-based fluorescence probe (AAFP) to detect cancer cells and frozen cancer tissue. This AAFP consisted of two fragments: aptamer TLS11a that targets HepG2 cells, and two short extending complementary DNA sequences with a 5′- and 3′-terminus that make the aptamer in hairpin structure a capable quencher to fluorophore. The ability of the AAFP to bind specifically to cancer cells was assessed using flow cytometry, fluorescence spectroscopy and fluorescence microscopy. Its ability to bind to frozen cancer tissue was assessed using fluorescence microscopy. As a result, in the absence of cancer cells, AAFP showed minimal fluorescence, reflecting auto-quenching. In the presence of cancer cells, however, AAFP showed a strong fluorescent signal. Therefore, this AAFP may be a promising tool for sensitive and specific detection of cancer.
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spelling pubmed-54288802017-05-15 An ‘activatable’ aptamer-based fluorescence probe for the detection of HepG2 cells Lai, Zongqiang Tan, Juntao Wan, Ruirong Tan, Jie Zhang, Zhenghua Hu, Zixi Li, Jieping Yang, Wei Wang, Yiwei Jiang, Yafeng He, Jian Yang, Nuo Lu, Xiaoling Zhao, Yongxiang Oncol Rep Articles It is significant to develop a probe with sensitivity and specificity for the detection of cancer cells. The present study aimed to develop an ‘activatable’ aptamer-based fluorescence probe (AAFP) to detect cancer cells and frozen cancer tissue. This AAFP consisted of two fragments: aptamer TLS11a that targets HepG2 cells, and two short extending complementary DNA sequences with a 5′- and 3′-terminus that make the aptamer in hairpin structure a capable quencher to fluorophore. The ability of the AAFP to bind specifically to cancer cells was assessed using flow cytometry, fluorescence spectroscopy and fluorescence microscopy. Its ability to bind to frozen cancer tissue was assessed using fluorescence microscopy. As a result, in the absence of cancer cells, AAFP showed minimal fluorescence, reflecting auto-quenching. In the presence of cancer cells, however, AAFP showed a strong fluorescent signal. Therefore, this AAFP may be a promising tool for sensitive and specific detection of cancer. D.A. Spandidos 2017-05 2017-03-24 /pmc/articles/PMC5428880/ /pubmed/28339076 http://dx.doi.org/10.3892/or.2017.5527 Text en Copyright: © Lai et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Lai, Zongqiang
Tan, Juntao
Wan, Ruirong
Tan, Jie
Zhang, Zhenghua
Hu, Zixi
Li, Jieping
Yang, Wei
Wang, Yiwei
Jiang, Yafeng
He, Jian
Yang, Nuo
Lu, Xiaoling
Zhao, Yongxiang
An ‘activatable’ aptamer-based fluorescence probe for the detection of HepG2 cells
title An ‘activatable’ aptamer-based fluorescence probe for the detection of HepG2 cells
title_full An ‘activatable’ aptamer-based fluorescence probe for the detection of HepG2 cells
title_fullStr An ‘activatable’ aptamer-based fluorescence probe for the detection of HepG2 cells
title_full_unstemmed An ‘activatable’ aptamer-based fluorescence probe for the detection of HepG2 cells
title_short An ‘activatable’ aptamer-based fluorescence probe for the detection of HepG2 cells
title_sort ‘activatable’ aptamer-based fluorescence probe for the detection of hepg2 cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428880/
https://www.ncbi.nlm.nih.gov/pubmed/28339076
http://dx.doi.org/10.3892/or.2017.5527
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