Bmi1 marks distinct castration-resistant luminal progenitor cells competent for prostate regeneration and tumour initiation

Nat Commun. 2016 Oct 5:7:12943. doi: 10.1038/ncomms12943.

Abstract

Identification of defined cell populations with stem/progenitor properties is key for understanding prostate development and tumorigenesis. Here we show that the polycomb repressor protein Bmi1 marks a population of castration-resistant luminal epithelial cells enriched in the mouse proximal prostate. We employ lineage tracing to show that these castration-resistant Bmi1-expressing cells (or CARBs) are capable of tissue regeneration and self-renewal. Notably, CARBs are distinct from the previously described luminal castration-resistant Nkx3.1-expressing cells (CARNs). CARBs can serve as a prostate cancer cell-of-origin upon Pten deletion, yielding luminal prostate tumours. Clonal analysis using the R26R-confetti allele indicates preferential tumour initiation from CARBs localized to the proximal prostate. These studies identify Bmi1 as a marker for a distinct population of castration-resistant luminal epithelial cells enriched in the proximal prostate that can serve as a cell of origin for prostate cancer.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Androgens / metabolism
  • Animals
  • Cell Lineage
  • Cell Transformation, Neoplastic / pathology
  • Epithelial Cells / metabolism
  • Male
  • Mice
  • Neoplastic Stem Cells / metabolism
  • PTEN Phosphohydrolase / metabolism
  • Polycomb Repressive Complex 1 / metabolism*
  • Prostate / cytology*
  • Prostatic Neoplasms, Castration-Resistant / drug therapy
  • Prostatic Neoplasms, Castration-Resistant / metabolism*
  • Proto-Oncogene Proteins / metabolism*
  • Recombination, Genetic
  • Regeneration*

Substances

  • Androgens
  • Bmi1 protein, mouse
  • Proto-Oncogene Proteins
  • Polycomb Repressive Complex 1
  • PTEN Phosphohydrolase
  • Pten protein, mouse