Jiang Zhong, Woda Bruce A, Wu Chin-Lee, Yang Ximing J
Department of Pathology, University of Massachusetts Medical School, Worcester 01655, USA.
Am J Clin Pathol. 2004 Aug;122(2):275-89. doi: 10.1309/EJUY-UQPE-X1MG-68MK.
The recent discovery of the overexpression of P504S/alpha-methylacyl coenzyme A racemase (AMACR) in prostate cancer is a successful example of translating an advanced molecular finding into clinical practice. AMACR (P504S) has been proven to be one of the few biomarkers that can help distinguish cancer from benign cells, with high sensitivity and specificity for prostate carcinoma. It is the first gene identified by the analysis of complementary DNA microarray profiles from prostate tissue to be used as a tissue tumor marker in clinical practice and to improve the diagnosis of prostate cancer. This review focuses on the study of AMACR (P504S) expression in prostate cancer, premalignant lesions, benign prostate tissues, and other normal and malignant tissues and a discussion of its clinical usefulness. We emphasize the interpretation of the AMACR immunohistochemical results in routine surgical pathology practice and also discuss the potential future applications of this marker and the possible role of AMACR in the pathogenesis of cancer development.
近期发现P504S/α-甲基酰基辅酶A消旋酶(AMACR)在前列腺癌中过表达,这是将先进分子研究成果转化为临床实践的成功范例。AMACR(P504S)已被证明是少数能够帮助区分癌细胞与良性细胞的生物标志物之一,对前列腺癌具有高敏感性和特异性。它是通过对前列腺组织互补DNA微阵列图谱分析鉴定出的首个基因,可在临床实践中用作组织肿瘤标志物,以改善前列腺癌的诊断。本文综述聚焦于AMACR(P504S)在前列腺癌、癌前病变、良性前列腺组织以及其他正常和恶性组织中的表达研究,并探讨其临床应用价值。我们着重阐述在常规外科病理实践中对AMACR免疫组化结果的解读,同时讨论该标志物未来可能的应用以及AMACR在癌症发生发展机制中可能发挥的作用。