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MAGI-2 Is a Sensitive and Specific Marker of Prostatic Adenocarcinoma: A Comparison With AMACR.
Goldstein, Jeffery; Goyal, Rajen; Roland, Joseph T; Gellert, Lan L; Clark, Peter E; Hameed, Omar; Giannico, Giovanna A.
Affiliation
  • Goldstein J; From the Department of Pathology, Microbiology, and Immunology.
  • Goyal R; From the Department of Pathology, Microbiology, and Immunology.
  • Roland JT; Department of Surgery.
  • Gellert LL; From the Department of Pathology, Microbiology, and Immunology.
  • Clark PE; Department of Urologic Surgery, Vanderbilt University Medical Center, Nashville, TN.
  • Hameed O; From the Department of Pathology, Microbiology, and Immunology Department of Urologic Surgery, Vanderbilt University Medical Center, Nashville, TN. omar.hameed@vanderbilt.edu.
  • Giannico GA; From the Department of Pathology, Microbiology, and Immunology.
Am J Clin Pathol ; 146(3): 294-302, 2016 Sep.
Article in En | MEDLINE | ID: mdl-27543977
ABSTRACT

OBJECTIVES:

We compared the utility of membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 (MAGI-2) and α-methylacyl CoA (AMACR) by immunohistochemistry in diagnosing prostatic adenocarcinoma.

METHODS:

Seventy-eight radical prostatectomies were used to construct three tissue microarrays with 512 cores, including benign prostatic tissue, benign prostatic hyperplasia, high-grade prostatic intraepithelial neoplasia (HGPIN), and adenocarcinoma. AMACR and MAGI-2 immunohistochemistry were evaluated by visual and image analysis.

RESULTS:

MAGI-2 and AMACR were significantly higher in adenocarcinoma and HGPIN compared with benign tissue. At H-score cutoffs of 300 and 200, MAGI-2 was more accurate in distinguishing benign from malignant glands than AMACR. Areas under the curve by image and visual analysis were 0.846 and 0.818 for MAGI-2 and 0.937 and 0.924 for AMACR, respectively. The accuracy of MAGI-2 in distinguishing benign from malignant glands on the same core was higher (95% vs 88%).

CONCLUSIONS:

MAGI-2 could represent a useful adjunct for diagnosis of prostatic adenocarcinoma, especially when AMACR is not discriminatory.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostate / Prostatic Hyperplasia / Prostatic Neoplasms / Adenocarcinoma / Carrier Proteins / Biomarkers, Tumor / Prostatic Intraepithelial Neoplasia / Racemases and Epimerases Type of study: Diagnostic_studies Limits: Humans / Male Language: En Journal: Am J Clin Pathol Year: 2016 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostate / Prostatic Hyperplasia / Prostatic Neoplasms / Adenocarcinoma / Carrier Proteins / Biomarkers, Tumor / Prostatic Intraepithelial Neoplasia / Racemases and Epimerases Type of study: Diagnostic_studies Limits: Humans / Male Language: En Journal: Am J Clin Pathol Year: 2016 Document type: Article