Cargando…
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...
Autores principales: | , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783235924224638976 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5428880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT laizongqiang anactivatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT tanjuntao anactivatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT wanruirong anactivatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT tanjie anactivatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT zhangzhenghua anactivatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT huzixi anactivatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT lijieping anactivatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT yangwei anactivatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT wangyiwei anactivatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT jiangyafeng anactivatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT hejian anactivatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT yangnuo anactivatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT luxiaoling anactivatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT zhaoyongxiang anactivatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT laizongqiang activatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT tanjuntao activatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT wanruirong activatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT tanjie activatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT zhangzhenghua activatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT huzixi activatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT lijieping activatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT yangwei activatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT wangyiwei activatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT jiangyafeng activatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT hejian activatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT yangnuo activatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT luxiaoling activatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells AT zhaoyongxiang activatableaptamerbasedfluorescenceprobeforthedetectionofhepg2cells |