BTF3 sustains cancer stem-like phenotype of prostate cancer via stabilization of BMI1

J Exp Clin Cancer Res. 2019 May 28;38(1):227. doi: 10.1186/s13046-019-1222-z.

Abstract

Background: Cancer stem-like traits contribute to prostate cancer (PCa) progression and metastasis. Deciphering the novel molecular mechanisms underlying stem-like traits may provide important insight for developing novel therapeutics.

Methods: Immunohistochemistry and immunofluorescence assays in prostatic tissues; gain- and loss-of-function analyses using ectopic overexpression and shRNAs in PCa cell lines; measurements of tumorigenic and stemness properties, and transcription in vitro and in vivo; transcriptional analysis in public databases.

Results: We identified that overexpression of BTF3 in PCa tissues and BTF3 expression highly correlates to stem-like traits. Cancer stem-like characteristics in PCa including self-renewal and metastatic potential were impaired by BTF3 loss and promoted by BTF3 overexpression. Mechanistically, BTF3 could stabilize BMI1, which is a crucial regulator of prostate stem cell self-renewal. More importantly, our data revealed that BTF3 is highly predictive of poor prognosis and may help in risk stratification of PCa patients.

Conclusions: BTF3 promotes PCa progression though modeling stem-like traits in PCa. BTF3 represents a stratification marker in PCa progression and outcomes.

Keywords: BMI1; BTF3; Cancer stem-like traits; Prostate cancer.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cell Proliferation
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Male
  • Mice
  • Neoplasm Grading
  • Neoplasm Invasiveness
  • Neoplasm Transplantation
  • Neoplastic Stem Cells / metabolism
  • Neoplastic Stem Cells / pathology*
  • Nuclear Proteins / metabolism*
  • Polycomb Repressive Complex 1 / chemistry*
  • Polycomb Repressive Complex 1 / metabolism
  • Prostatic Neoplasms / metabolism
  • Prostatic Neoplasms / pathology*
  • Protein Stability
  • Survival Analysis
  • Transcription Factors / metabolism*
  • Up-Regulation

Substances

  • BMI1 protein, human
  • Nuclear Proteins
  • Transcription Factors
  • transcription factor BTF3
  • Polycomb Repressive Complex 1