A cancer cell-activatable aptamer-reporter system for one-step assay of circulating tumor cells

42Citations
Citations of this article
69Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

The current antibody-mediated numeration assays of circulating tumor cells (CTCs) require multiple steps and are timeconsuming. To overcome these technical limitations, a cancer cell-activatable aptamer-reporter was formulated by conjugating a biomarker-specific aptamer sequence with paired fluorochrome-quencher molecules. In contrast to the antibody probes, the intact aptamer-reporter was optically silent in the absence of cells of interest. However, when used in an assay, the aptamer selectively targeted cancer cells through interaction with a specific surface biomarker, which triggered internalization of the aptamer-reporter and, subsequently, into cell lysosomes. Rapid lysosomal degradation of the aptamer-reporter resulted in separation of the paired fluorochrome-quencher molecules. The released fluorochrome emitted bright fluorescent signals exclusively within the targeted cancer cells, with no background noise in the assay. Thus, the assays could be completed in a single step within minutes. By using this one-step assay, CTCs in whole blood and marrow aspirate samples of patients with lymphoma tumors were selectively highlighted and rapidly detected with no off-target signals from background blood cells. The development of the cancer cell-activatable aptamer-reporter system allows for the possibility of a simple and robust point-ofcare test for CTC detection, which is currently unavailable. © 2014 The American Society of Gene & Cell Therapy All rights reserved.

Cite

CITATION STYLE

APA

Zeng, Z., Tung, C. H., & Zu, Y. (2014). A cancer cell-activatable aptamer-reporter system for one-step assay of circulating tumor cells. Molecular Therapy Nucleic Acids, 3, e184. https://doi.org/10.1038/mtna.2014.36

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free