Wnt-responsive cancer stem cells are located close to distorted blood vessels and not in hypoxic regions in a p53-null mouse model of human breast cancer

  • Tegy J. Vadakkan
  • , John D. Landua
  • , Wen Bu
  • , Wei Wei
  • , Fuhai Li
  • , Stephen T.C. Wong
  • , Mary E. Dickinson
  • , Jeffrey M. Rosen
  • , Michael T. Lewis
  • , Mei Zhang

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Cancer stem cells (CSCs, or tumor-initiating cells) may be responsible for tumor formation in many types of cancer, including breast cancer. Using high-resolution imaging techniques, we analyzed the relationship between a Wnt-responsive, CSC-enriched population and the tumor vasculature using p53-null mouse mammary tumors transduced with a lentiviral Wnt signaling reporter. Consistent with their localization in the normal mammary gland, Wnt-responsive cells in tumors were enriched in the basal/myoepithelial population and generally located in close proximity to blood vessels. The Wnt-responsive CSCs did not colocalize with the hypoxia-inducible factor 1α-positive cells in these p53-null basal-like tumors. Average vessel diameter and vessel tortuosity were increased in p53-null mouse tumors, as well as in a human tumor xenograft as compared with the normal mammary gland. The combined strategy of monitoring the fluorescently labeled CSCs and vasculature using high-resolution imaging techniques provides a unique opportunity to study the CSC and its surrounding vasculature.

Original languageEnglish
Pages (from-to)857-866
Number of pages10
JournalStem Cells Translational Medicine
Volume3
Issue number7
DOIs
StatePublished - 2014

Keywords

  • Cancer stem cells
  • In vivo optical imaging
  • Microvasculature
  • P53
  • Signal transduction
  • Stem cell microenvironment

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