Crosstalk Between Androgen-sensitive and Androgen-insensitive Prostate Cancer Cells

Anticancer Res. 2018 Apr;38(4):2045-2055. doi: 10.21873/anticanres.12444.

Abstract

Aim: To investigate how androgen-sensitive LNCaP cells crosstalk with androgen-insensitive DU145 or PC-3 cells.

Materials and methods: The numbers of LNCaP cells were counted when co-cultured with DU145 or PC-3 cells and vise versa. Androgen receptor (AR) activity in LNCaP cells was examined by luciferase reporter assay after transfection with a luciferase reporter driven by PSA promoter in the presence of DU145 or PC-3 cells. Concentration of androgens in the medium was measured by liquid chromatography-mass spectrometry (LC-MS/MS). The ability of migration and invasion of PC-3 and DU145 cells was investigated using a 2-layer chamber, in the presence of LNCaP cells.

Results: Co-culture of LNCaP cells with DU145 cells resulted in the conversion of dehydroepiandrosterone (DHEA) to dihydrotestosterone (DHT), which stimulated cell proliferation and PSA promoter activity in LNCaP cells. The increased cell proliferation rate and AR activity, induced in LNCaP cells after DHT treatment, was further enhanced by co-culture with DU145 cells. LNCaP cells also stimulated the proliferation of DU145 and PC-3 cells, via secreting soluble factors. Finally, LNCaP cells promoted migration and invasion of PC-3 cells, in a co-culture system; however inhibited migration and invasion of DU145 cells.

Conclusion: Crosstalk between androgen-sensitive PCa cells and androgen-insensitive PCa cells might develop the progression of PCa.

Keywords: Prostate cancer; androgen; androgen-insensitive; androgen-sensitive.

MeSH terms

  • Androgen Antagonists / pharmacology
  • Androgen Antagonists / therapeutic use
  • Androgens / metabolism*
  • Cell Communication / drug effects
  • Cell Communication / physiology*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Coculture Techniques
  • Drug Resistance, Neoplasm
  • Humans
  • Male
  • Prostatic Neoplasms / metabolism*
  • Prostatic Neoplasms / pathology*
  • Prostatic Neoplasms, Castration-Resistant / metabolism*
  • Prostatic Neoplasms, Castration-Resistant / pathology*
  • Receptors, Androgen / metabolism
  • Signal Transduction / drug effects

Substances

  • Androgen Antagonists
  • Androgens
  • Receptors, Androgen