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Journal of Clinical Pathology 2003;56:892-897; doi:10.1136/jcp.56.12.892
Copyright © 2003 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists.
Journal of Clinical Pathology 2003;56:892-897
© 2003 BMJ Publishing Group Ltd & Association of Clinical Pathologists

REVIEW

{alpha}-Methylacyl CoA racemase (P504S): overview and potential uses in diagnostic pathology as applied to prostate needle biopsies

A J Evans

Correspondence to:
Correspondence to:
Dr A J Evans
Department of Laboratory Medicine and Pathobiology, University of Toronto, University Health Network, Room 4-302, Princess Margaret Hospital, 610 University Avenue, Toronto, Ontario, Canada, M5G 2M9;andrew.evans{at}uhn.on.ca

ABSTRACT

The diagnosis of prostatic adenocarcinoma remains dependent on the recognition of basic haematoxylin and eosin criteria. The discovery of {alpha}-methylacyl CoA racemase/P504S (AMACR/P504S) overexpression in prostate cancer represents a triumph of high throughput microarray technology, and is a powerful demonstration of how this methodology can be used to facilitate the rapid development of diagnostically relevant antibodies. Immunohistochemistry with anti-AMACR/P504S is useful for detecting prostate cancer in the full range of prostate specimens encountered in surgical pathology, be they needle biopsies, transurethral resection of prostate chips, or prostatectomies. In particular, studies to date with AMACR/P504S clearly demonstrate the ability of this marker to support a diagnosis of malignancy in prostate needle biopsies. This is particularly true when it is combined with negative staining for a basal cell marker, such as 34ßE12 or p63. Although it has limitations with respect to sensitivity and specificity, AMACR/P504S will no doubt become a standard adjunctive stain used by pathologists seeking to reach a definitive diagnosis in prostate biopsies considered to be atypical, but not diagnostic of malignancy on haematoxylin and eosin sections alone.

Keywords: {alpha}-Methylacyl CoA racemase; prostate needle biopsies; diagnosis????

Abbreviations: AAH, atypical adenomatous hyperplasia; AMACR, {alpha}-methylacyl CoA racemase; HGPIN, high grade prostatic intraepithelial neoplasia; H&E, haematoxylin and eosin; PSA, prostate specific antigen; TURP, transurethral resection of prostate


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This article has been cited by other articles:

  • Hughes, C, Murphy, A, Martin, C, Sheils, O, O'Leary, J (2005). Molecular pathology of prostate cancer. J. Clin. Pathol. 58: 673-684 [Abstract] [Full Text]  
  • Savolainen, K., Kotti, T. J., Schmitz, W., Savolainen, T. I., Sormunen, R. T., Ilves, M., Vainio, S. J., Conzelmann, E., Hiltunen, J. K. (2004). A mouse model for {alpha}-methylacyl-CoA racemase deficiency: adjustment of bile acid synthesis and intolerance to dietary methyl-branched lipids. Hum Mol Genet 13: 955-965 [Abstract] [Full Text]  

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