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A flexible reporter system for direct observation and isolation of cancer stem cells.
Tang, Binwu; Raviv, Asaf; Esposito, Dominic; Flanders, Kathleen C; Daniel, Catherine; Nghiem, Bao Tram; Garfield, Susan; Lim, Langston; Mannan, Poonam; Robles, Ana I; Smith, William I; Zimmerberg, Joshua; Ravin, Rea; Wakefield, Lalage M.
Afiliación
  • Tang B; Laboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, MD 20892, USA.
  • Raviv A; Laboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, MD 20892, USA.
  • Esposito D; Protein Expression Laboratory, Advanced Technology Program, Frederick National Laboratory for Cancer Research, Frederick, MD 21701, USA.
  • Flanders KC; Laboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, MD 20892, USA.
  • Daniel C; Laboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, MD 20892, USA.
  • Nghiem BT; Laboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, MD 20892, USA.
  • Garfield S; Confocal Microscopy Core, National Cancer Institute, Bethesda, MD 20892, USA.
  • Lim L; Confocal Microscopy Core, National Cancer Institute, Bethesda, MD 20892, USA.
  • Mannan P; Confocal Microscopy Core, National Cancer Institute, Bethesda, MD 20892, USA.
  • Robles AI; Laboratory of Human Carcinogenesis, National Cancer Institute, Bethesda, MD 20892 USA.
  • Smith WI; Department of Pathology, Suburban Hospital, Bethesda, MD 20814, USA.
  • Zimmerberg J; Program in Physical Biology, National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.
  • Ravin R; Program in Physical Biology, National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.
  • Wakefield LM; Laboratory of Cancer Biology and Genetics, National Cancer Institute, Bethesda, MD 20892, USA. Electronic address: lw34g@nih.gov.
Stem Cell Reports ; 4(1): 155-169, 2015 Jan 13.
Article en En | MEDLINE | ID: mdl-25497455
ABSTRACT
Many tumors are hierarchically organized with a minority cell population that has stem-like properties and enhanced ability to initiate tumorigenesis and drive therapeutic relapse. These cancer stem cells (CSCs) are typically identified by complex combinations of cell-surface markers that differ among tumor types. Here, we developed a flexible lentiviral-based reporter system that allows direct visualization of CSCs based on functional properties. The reporter responds to the core stem cell transcription factors OCT4 and SOX2, with further selectivity and kinetic resolution coming from use of a proteasome-targeting degron. Cancer cells marked by this reporter have the expected properties of self-renewal, generation of heterogeneous offspring, high tumor- and metastasis-initiating activity, and resistance to chemotherapeutics. With this approach, the spatial distribution of CSCs can be assessed in settings that retain microenvironmental and structural cues, and CSC plasticity and response to therapeutics can be monitored in real time.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Asunto principal: Células Madre Neoplásicas / Expresión Génica / Genes Reporteros Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Stem Cell Reports Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Asunto principal: Células Madre Neoplásicas / Expresión Génica / Genes Reporteros Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Stem Cell Reports Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos