Title | A cancer cell-activatable aptamer-reporter system for one-step assay of circulating tumor cells. |
Publication Type | Journal Article |
Year of Publication | 2014 |
Authors | Zeng Z, Tung C-H, Zu Y |
Journal | Mol Ther Nucleic Acids |
Volume | 3 |
Pagination | e184 |
Date Published | 2014 Aug 12 |
ISSN | 2162-2531 |
Abstract | The current antibody-mediated numeration assays of circulating tumor cells (CTCs) require multiple steps and are time-consuming. 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-of-care test for CTC detection, which is currently unavailable. |
DOI | 10.1038/mtna.2014.36 |
Alternate Journal | Mol Ther Nucleic Acids |
PubMed ID | 25118170 |
PubMed Central ID | PMC4221596 |
Grant List | R01 CA151955 / CA / NCI NIH HHS / United States R33 CA173382 / CA / NCI NIH HHS / United States |
Related Institute:
Molecular Imaging Innovations Institute (MI3)