| Literature DB >> 29778888 |
Yingying Geng1, Hira L Goel2, Ngoc B Le3, Tatsuyuki Yoshii3, Rubul Mout3, Gulen Y Tonga3, John J Amante2, Arthur M Mercurio2, Vincent M Rotello4.
Abstract
Cancer stem cells (CSCs) contribute to multidrug resistance, tumor recurrence and metastasis, making them prime therapeutic targets. Their ability to differentiate and lose stem cell properties makes them challenging to study. Currently, there is no simple assay that can quickly capture and trace the dynamic phenotypic changes on the CSC surface. Here, we report rapid discrimination of breast CSCs from non-CSCs using a nanoparticle-fluorescent-protein based sensor. This nanosensor was employed to discriminate CSCs from non-CSCs, as well as CSCs that had differentiated in vitro in two breast cancer models. Importantly, the sensor platform could also discriminate CSCs from the bulk population of cells in patient-derived xenografts of human breast cancer. Taken together, the results obtained demonstrate the feasibility of using the nanosensor to phenotype CSCs and monitor their fate. Furthermore, this approach provides a novel area for therapeutic interventions against these challenging targets.Entities:
Keywords: Array-based sensing; Cancer stem cell; Discrimination; Patient-derived xenografts; Personalized medicine
Mesh:
Year: 2018 PMID: 29778888 PMCID: PMC6535092 DOI: 10.1016/j.nano.2018.05.009
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307