Hic-5 influences genomic and non-genomic actions of the androgen receptor in prostate myofibroblasts

Mol Cell Endocrinol. 2014 Mar 25;384(1-2):185-99. doi: 10.1016/j.mce.2014.01.004. Epub 2014 Jan 17.

Abstract

There is extensive knowledge of androgen receptor (AR) signaling in cancer cells, but less regarding androgen action in stromal cells of the tumor microenvironment. We report here the genome-wide effects of a stromal cell specific molecular adapter and AR coregulator, hydrogen peroxide-inducible gene 5 (Hic-5/TGFB1I1), on AR function in prostate myofibroblasts. Following androgen stimulation, Hic-5 rapidly translocates to the nucleus, coincident with increased phosphorylation of focal adhesion kinase. As a coregulator, Hic-5 acted to amplify or inhibit regulation of approximately 50% of AR target genes, affected androgen regulation of growth, cell adhesion, motility and invasion. These data suggest Hic-5 as a transferable adaptor between focal adhesions and the nucleus of prostate myofibroblasts, where it acts a key mediator of the specificity and sensitivity of AR signaling. We propose a model in which Hic-5 coordinates AR signaling with adhesion and extracellular matrix contacts to regulate cell behavior in the tumor microenvironment.

Keywords: Androgen receptor; Fibroblasts; Focal adhesions; Microenvironment; Prostate cancer; Stroma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Androgens / pharmacology
  • Cell Adhesion
  • Cell Line, Transformed
  • Cell Movement
  • Cell Nucleus / metabolism
  • Focal Adhesion Protein-Tyrosine Kinases / genetics*
  • Focal Adhesion Protein-Tyrosine Kinases / metabolism
  • Focal Adhesions / metabolism
  • Gene Expression Regulation
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Intracellular Signaling Peptides and Proteins / metabolism
  • LIM Domain Proteins / genetics*
  • LIM Domain Proteins / metabolism
  • Male
  • Molecular Sequence Annotation
  • Myofibroblasts / cytology
  • Myofibroblasts / drug effects
  • Myofibroblasts / metabolism*
  • Phosphorylation
  • Prostate / metabolism
  • Prostate / pathology
  • Protein Transport
  • Receptors, Androgen / genetics*
  • Receptors, Androgen / metabolism
  • Signal Transduction
  • Stromal Cells / cytology
  • Stromal Cells / drug effects
  • Stromal Cells / metabolism*
  • Testosterone / pharmacology
  • Tumor Microenvironment

Substances

  • AR protein, human
  • Androgens
  • Intracellular Signaling Peptides and Proteins
  • LIM Domain Proteins
  • Receptors, Androgen
  • TGFB1I1 protein, human
  • Testosterone
  • Focal Adhesion Protein-Tyrosine Kinases