A flexible reporter system for direct observation and isolation of cancer stem cells

Stem Cell Reports. 2015 Jan 13;4(1):155-169. doi: 10.1016/j.stemcr.2014.11.002. Epub 2014 Dec 11.

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.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • Asymmetric Cell Division
  • Cell Differentiation
  • Cell Line, Tumor
  • Cell Movement / genetics
  • Cell Tracking
  • Cell Transformation, Neoplastic / genetics
  • Drug Resistance, Neoplasm / genetics
  • Embryonic Stem Cells / cytology
  • Embryonic Stem Cells / metabolism
  • Gene Expression*
  • Gene Order
  • Genes, Reporter*
  • Genetic Vectors
  • Heterografts
  • Humans
  • Immunophenotyping
  • Mice
  • Neoplastic Stem Cells / drug effects
  • Neoplastic Stem Cells / metabolism*
  • Neoplastic Stem Cells / pathology
  • Phenotype
  • Promoter Regions, Genetic
  • Protein Binding
  • Response Elements
  • Transcription Factors / metabolism
  • Tumor Cells, Cultured

Substances

  • Antineoplastic Agents
  • Transcription Factors