Alpha-methylacyl-CoA racemase (AMACR) in fine-needle aspiration specimens of prostate lesions

Gordana Kaić1, Cedna Tomasović-Loncarić

  • 1Department of Clinical Cytology and Cytometry, University Hospital Dubrava, Zagreb, Croatia. gordana.kaic@zg.t-com.hr

Insights

The P504S gene and alpha-methylacyl-CoA racemase (AMACR) show potential as prostate cancer markers. Their expression in fine-needle aspirates correlates with cell differentiation, aiding cytodiagnosis.

Area of Science:

  • Oncology
  • Molecular Pathology
  • Urology

Background:

  • Prostate cancer diagnosis relies on accurate cytological evaluation.
  • The P504S gene and its protein product, alpha-methylacyl-CoA racemase (AMACR), are implicated in prostate cancer development.
  • Identifying reliable molecular markers is crucial for improving diagnostic accuracy.

Purpose of the Study:

  • To investigate the expression of P504S/AMACR in fine-needle aspiration (FNA) smears of prostate lesions.
  • To correlate P504S/AMACR expression patterns with cytological diagnoses, including carcinoma, atypia, and benign hyperplasia.
  • To assess the utility of P504S/AMACR as a molecular marker in prostate cancer cytodiagnosis.

Main Methods:

  • Immunocytochemistry was employed to detect P504S/AMACR expression.
  • The study included 35 patients with FNA diagnoses: prostate carcinoma (n=16), atypia (n=15), and benign hyperplasia (n=4).
  • Expression was analyzed qualitatively (focal/diffuse) and quantitatively (percentage of positive cells).

Main Results:

  • Benign cases exhibited no P504S/AMACR expression.
  • 75% of malignant cases showed positive P504S/AMACR staining, often weak and focal or diffuse in a small cell percentage.
  • Intensive staining was observed in low-grade carcinomas and some atypical cases, suggesting a correlation with cell differentiation.

Conclusions:

  • P504S/AMACR expression correlates with the differentiation of prostate cells.
  • P504S/AMACR staining in FNA smears may significantly enhance the cytodiagnosis of prostate lesions.
  • This approach offers molecular-level characterization of prostate tissues obtained via FNA.

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