Immunohistochemical characterization of neuroendocrine cells in prostate cancer

Prostate. 2006 Sep 15;66(13):1399-406. doi: 10.1002/pros.20434.

Abstract

Background: Neuroendocrine (NE) cells increase in high grade/stage prostate cancer (PC) and may contribute to androgen-independent cancer. Their immunohistochemical phenotype has not been studied in detail and conflicting results have been reported.

Methods: PC tissue was stained immunohistochemically for luminal secretory cell-associated cytokeratin, basal cell markers, ki-67, androgen receptor (AR), PSA, prostate acid phosphatase (PAP), and alpha-methylacyl coenzyme A racemase (AMACR).

Results: The NE cells are positive for AE1/AE3, Cam 5.2, and negative for basal cell markers. They are negative for AR, PSA, and Ki-67 but positive for PAP. The benign NE cells are negative for AMACR while the malignant NE cells are positive for AMACR.

Conclusions: NE cells of PC constitute a unique subset of cancer cells, which have a unique immunohistochemical profile. They do not express AR, consistent with their resistance to hormonal therapy. They are post-mitotic cells but are malignant and part of the tumor.

MeSH terms

  • Acid Phosphatase / genetics
  • Acid Phosphatase / metabolism
  • Androgen Antagonists / pharmacology
  • Drug Resistance, Neoplasm
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunohistochemistry
  • Keratins / genetics
  • Keratins / metabolism
  • Ki-67 Antigen / genetics
  • Ki-67 Antigen / metabolism
  • Male
  • Neuroendocrine Tumors / metabolism*
  • Neuroendocrine Tumors / pathology*
  • Phenotype
  • Prostate-Specific Antigen / genetics
  • Prostate-Specific Antigen / metabolism
  • Prostatic Neoplasms / metabolism*
  • Prostatic Neoplasms / pathology*
  • Racemases and Epimerases / genetics
  • Racemases and Epimerases / metabolism
  • Receptors, Androgen / genetics
  • Receptors, Androgen / metabolism

Substances

  • Androgen Antagonists
  • Ki-67 Antigen
  • Receptors, Androgen
  • Keratins
  • Acid Phosphatase
  • Prostate-Specific Antigen
  • Racemases and Epimerases
  • alpha-methylacyl-CoA racemase