2016
DOI: 10.1007/7651_2016_360
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Reporter Systems to Study Cancer Stem Cells

Abstract: Cancer stem cells have been identified in primary tumors, patient derived xenografts, and established cancer cell lines. The development of reporters has enabled investigators to rapidly enrich for these cells and more importantly track these cells in real time. Here we describe the current state of the reporter field and their use and limitations in multiple cancers.

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Cited by 10 publications
(14 citation statements)
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“…This indicates the need to use multiple markers to identify CSCs from different subclones. Reporter-based approaches to functionally define CSCs based on their expression of core pluripotency genes (e.g., NANOG) or CSC-specific signaling pathways (e.g., Wnt pathway) provide another opportunity to study CSCs in pre-clinical models (Saygin et al, 2016). For two decades, these markers have been valuable tools for clinical correlative and prognostic analyses, and their longitudinal assessment during clinical tumor progression improved our understanding of CSC evolution dynamics.…”
Section: Identification Of Cscsmentioning
confidence: 99%
“…This indicates the need to use multiple markers to identify CSCs from different subclones. Reporter-based approaches to functionally define CSCs based on their expression of core pluripotency genes (e.g., NANOG) or CSC-specific signaling pathways (e.g., Wnt pathway) provide another opportunity to study CSCs in pre-clinical models (Saygin et al, 2016). For two decades, these markers have been valuable tools for clinical correlative and prognostic analyses, and their longitudinal assessment during clinical tumor progression improved our understanding of CSC evolution dynamics.…”
Section: Identification Of Cscsmentioning
confidence: 99%
“…For that reason, fluorescence reporter systems driven by portions of promoters where these proteins bind were developed to allow CSCs to be labeled and tracked in various types of cancer. These reporter systems seem to be a powerful tool to identify and study CSCs more efficiently than cell-surface markers (Saygin et al, 2016). Tang et al (2015) developed a flexible lentiviral-based reporter system (SORE6-GFP) that allows direct visualization of CSCs based on SOX2 and OCT4 expression.…”
Section: Transcription Factors As Potential Csc Markersmentioning
confidence: 99%
“…The design of reporter systems is typically based on the fact that transcription factors, such as NANOG, sex-determining region Y-box (SOX)2, organic cation/carnitine transporter (OCT) 4, and self-renewal pathways, such as NOTCH and WNT, are upregulated in CSCs [44]. Reporter systems can mark stem cells based on this upregulated transcription factor expression using a model system that contains a genetic construct that leads to expression of a tagged (typically fluorescent) transcription factor protein when the gene of interest is transcriptionally activated in cells.…”
Section: The Use Of Reporter Systems Based On Stem Cell Transcriptionmentioning
confidence: 99%