Expression of BAG-1 protein correlates with aggressive behavior of prostate cancers

Prostate. 2006 Jun 1;66(8):801-10. doi: 10.1002/pros.20384.

Abstract

Background: Differences in tumor behavior, ranging from indolent to aggressive, create a need for novel prognostic biomarkers. BAG-1 is a co-chaperone that regulates the activity of Hsp70, Bcl-2, Raf-1, growth factor, and steroid receptors (e.g., the Androgen Receptor).

Methods: Using immunohistochemical method, we explored BAG-1 expression in prostate cancers and its association with clinicopathological parameters.

Results: BAG-1 immunostaining was elevated in prostate cancer compared to normal prostatic epithelium. Higher nuclear BAG-1 in hormone-refractory (n = 34) compared to localized untreated tumors (n = 58) (P < 0.0001) suggested that upregulation of the nuclear isoform may contribute to disease progression. In 64 early-stage patients (T2N0M0) treated with external-beam irradiation, cytosolic BAG-1 correlated with higher pretreatment levels of serum Prostate specific antigen (P = 0.04) and shorter time to disease progression (P = 0.00004).

Conclusions: Increased cytosolic and nuclear BAG-1 expression may denote more aggressive variants of prostate cancer.

Publication types

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

MeSH terms

  • Biomarkers, Tumor / analysis
  • Cell Nucleus / chemistry
  • Cytosol / chemistry
  • DNA-Binding Proteins / analysis
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Data Interpretation, Statistical
  • Disease Progression
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunohistochemistry
  • Male
  • Neoplasm Invasiveness
  • Prognosis
  • Prostate / chemistry
  • Prostate-Specific Antigen / blood
  • Prostatic Neoplasms / blood
  • Prostatic Neoplasms / metabolism*
  • Prostatic Neoplasms / pathology*
  • Prostatic Neoplasms / radiotherapy
  • Transcription Factors / analysis
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • BCL2-associated athanogene 1 protein
  • Biomarkers, Tumor
  • DNA-Binding Proteins
  • Transcription Factors
  • Prostate-Specific Antigen