A chimeric virus-based probe unambiguously detects live circulating tumor cells with high specificity and sensitivity
The current methods for detecting circulating tumor cells (CTCs) suffer from several drawbacks. We report a novel method that is based on a chimeric virus probe and can detect CTCs with extremely high specificity and sensitivity. Moreover, it exclusively detects live CTCs, and its detection efficacy...
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2021-12-01
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doaj-fc8471d0e6d84a4085c28401103e58a72021-09-27T04:26:42ZengElsevierMolecular Therapy: Methods & Clinical Development2329-05012021-12-01237886A chimeric virus-based probe unambiguously detects live circulating tumor cells with high specificity and sensitivityXinping Fu0Lihua Tao1Xiaoliu Zhang2Department of Biology and Biochemistry and Center for Nuclear Receptor and Cell Signaling, University of Houston, Houston, TX 77204, USADepartment of Biology and Biochemistry and Center for Nuclear Receptor and Cell Signaling, University of Houston, Houston, TX 77204, USADepartment of Biology and Biochemistry and Center for Nuclear Receptor and Cell Signaling, University of Houston, Houston, TX 77204, USA; Corresponding author: Xiaoliu Zhang, Department of Biology and Biochemistry and Center for Nuclear Receptor and Cell Signaling, University of Houston, Houston, TX 77204, USA.The current methods for detecting circulating tumor cells (CTCs) suffer from several drawbacks. We report a novel method that is based on a chimeric virus probe and can detect CTCs with extremely high specificity and sensitivity. Moreover, it exclusively detects live CTCs, and its detection efficacy is not impacted by the variation of epithelial cell adhesion molecule (EpCAM) expression. The chimeric virus probe is composed of a capsid from human papillomavirus that provides the detection with high specificity and an SV40-based genome that can amplify extensively inside CTCs and, hence, endows the detection with high sensitivity. Furthermore, different marker genes can be incorporated into the probe to provide detection with versatility. These unique capabilities will likely improve the validity and utility of this CTC detection in several clinical applications, which is one of the drawbacks suffered by many of the current CTC detection methods.http://www.sciencedirect.com/science/article/pii/S2329050121001339circulating tumor cellschimeric viral vectorhuman papillomavirusSV40probeGFP |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xinping Fu Lihua Tao Xiaoliu Zhang |
spellingShingle |
Xinping Fu Lihua Tao Xiaoliu Zhang A chimeric virus-based probe unambiguously detects live circulating tumor cells with high specificity and sensitivity Molecular Therapy: Methods & Clinical Development circulating tumor cells chimeric viral vector human papillomavirus SV40 probe GFP |
author_facet |
Xinping Fu Lihua Tao Xiaoliu Zhang |
author_sort |
Xinping Fu |
title |
A chimeric virus-based probe unambiguously detects live circulating tumor cells with high specificity and sensitivity |
title_short |
A chimeric virus-based probe unambiguously detects live circulating tumor cells with high specificity and sensitivity |
title_full |
A chimeric virus-based probe unambiguously detects live circulating tumor cells with high specificity and sensitivity |
title_fullStr |
A chimeric virus-based probe unambiguously detects live circulating tumor cells with high specificity and sensitivity |
title_full_unstemmed |
A chimeric virus-based probe unambiguously detects live circulating tumor cells with high specificity and sensitivity |
title_sort |
chimeric virus-based probe unambiguously detects live circulating tumor cells with high specificity and sensitivity |
publisher |
Elsevier |
series |
Molecular Therapy: Methods & Clinical Development |
issn |
2329-0501 |
publishDate |
2021-12-01 |
description |
The current methods for detecting circulating tumor cells (CTCs) suffer from several drawbacks. We report a novel method that is based on a chimeric virus probe and can detect CTCs with extremely high specificity and sensitivity. Moreover, it exclusively detects live CTCs, and its detection efficacy is not impacted by the variation of epithelial cell adhesion molecule (EpCAM) expression. The chimeric virus probe is composed of a capsid from human papillomavirus that provides the detection with high specificity and an SV40-based genome that can amplify extensively inside CTCs and, hence, endows the detection with high sensitivity. Furthermore, different marker genes can be incorporated into the probe to provide detection with versatility. These unique capabilities will likely improve the validity and utility of this CTC detection in several clinical applications, which is one of the drawbacks suffered by many of the current CTC detection methods. |
topic |
circulating tumor cells chimeric viral vector human papillomavirus SV40 probe GFP |
url |
http://www.sciencedirect.com/science/article/pii/S2329050121001339 |
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