Issue 7, 2020

Capture and selective release of multiple types of circulating tumor cells using smart DNAzyme probes

Abstract

The effective capture, release and reanalysis of circulating tumor cells (CTCs) are of great significance to acquire tumor information and promote the progress of tumor therapy. Particularly, the selective release of multiple types of CTCs is critical to further study; however, it is still a great challenge. To meet this challenge, we designed a smart DNAzyme probe-based platform. By combining multiple targeting aptamers and multiple metal ion responsive DNAzymes, efficient capture and selective release of multiple types CTCs were realized. Sgc8c aptamer integrated Cu2+-dependent DNAzyme and TD05 aptamer integrated Mg2+-dependent DNAzyme can capture CCRF-CEM cells and Ramos cells respectively on the substrate. With the addition of Cu2+ or Mg2+, CCRF-CEM cells or Ramos cells will be released from the substrate with specific selectivity. Furthermore, our platform has been successfully demonstrated in the whole blood sample. Therefore, our capture/release platform will benefit research on the molecular analysis of CTCs after release and has great potential for cancer diagnosis and individualized treatment.

Graphical abstract: Capture and selective release of multiple types of circulating tumor cells using smart DNAzyme probes

Supplementary files

Article information

Article type
Edge Article
Submitted
27 Aug 2019
Accepted
06 Jan 2020
First published
09 Jan 2020
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2020,11, 1948-1956

Capture and selective release of multiple types of circulating tumor cells using smart DNAzyme probes

Q. Zhang, W. Wang, S. Huang, S. Yu, T. Tan, J. Zhang and J. Zhu, Chem. Sci., 2020, 11, 1948 DOI: 10.1039/C9SC04309H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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