| Literature DB >> 25920950 |
Steven McClellan1, Jaroslav Slamecka2, Patrick Howze2, Lee Thompson2, Michael Finan2, Rodney Rocconi2, Laurie Owen2.
Abstract
Cancer stem cells (CSC) are a distinct subpopulation within a tumor shown to drive tumor progression, metastasis, and recurrence. A review of the literature reveals poor consensus, with the use of a wide variety of surface markers and functional assays to identify and isolate cancer stem cells. Utilizing a novel technology that enables live-cell mRNA quantitation, we have demonstrated the ability to identify and sort viable CSC based on markers associated with stemness in pluripotent cells. Fresh tumor samples from a variety of cancer types were examined by flow cytometry for Nanog expression. Levels of CSC detected ranged from 6% to 19%. This method of CSC detection was cross-validated with other commonly used surface markers with good correlation. Matrigel invasion assays confirmed that CSC isolated using this method are both highly motile and invasive. This approach simplifies the process of identifying viable CSC from fresh tumor tissue, providing a level of accuracy not previously available. This method may also provide a valuable tool for screening and validating new CSC biomarkers.Entities:
Keywords: Alkaline phosphatase; Cancer stem cell; Live cell mRNA detection; Nanog; SmartFlare nanoprobe
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Year: 2015 PMID: 25920950 DOI: 10.1016/j.ymeth.2015.04.022
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608