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在405份前列腺标本(包括376份18号针穿刺活检标本)中进行P504S免疫组化检测。

P504S immunohistochemical detection in 405 prostatic specimens including 376 18-gauge needle biopsies.

作者信息

Beach R, Gown A M, De Peralta-Venturina M N, Folpe A L, Yaziji H, Salles P G, Grignon D J, Fanger G R, Amin M B

机构信息

Department of Pathology and Laboratory Medicine, Emory University Hospital, 1364 Clifton Road NE, Atlanta, GA 30322, USA.

出版信息

Am J Surg Pathol. 2002 Dec;26(12):1588-96. doi: 10.1097/00000478-200212000-00006.

Abstract

P504S is a recently described, prostate cancer-specific gene that encodes a protein involved in the beta-oxidation of branched chain fatty acids. A recent study has shown that immunohistochemical detection of P504S gene product is a sensitive and specific marker of prostatic carcinoma in formalin-fixed, paraffin-embedded tissues. We performed a detailed analysis of P504S protein expression in a large series of prostate and bladder specimens with special emphasis on staining in specific morphologic patterns of prostatic adenocarcinoma, posthormonal and radiation therapy cases, and invasive urothelial carcinoma. A total of 366 prostate needle core biopsies from 124 patients with prostate cancer, 10 biopsies from 2 patients without prostate cancer, 28 prostatectomy specimens (16 with specific morphologic patterns, 7 posthormonal therapy and 5 postradiation therapy specimens), 5 bladder specimens with invasive urothelial carcinoma, and a single transurethral resection specimen from a patient with hormonally treated prostate cancer and invasive urothelial carcinoma were stained with P504S monoclonal antibody at a 1:250 dilution using standard heat-induced epitope retrieval and avidin-biotin technique. Extent (0, no staining; 1+, 1-10% staining; 2+, 11-50% staining; 3+, > or =51% staining) and location (luminal, subluminal, and diffuse cytoplasmic) of immunoreactivity in carcinoma and benign tissues were recorded. A total of 153 of 186 biopsies (82%) with prostatic adenocarcinoma stained for P504S. Pseudohyperplastic, atrophic, ductal, and mucinous prostatic carcinomas stained similarly, as did cases treated with hormone or radiotherapy. In 81 of 377 (21%) foci of benign prostatic tissue there was staining that was almost always focal, faint, and noncircumferential. Seminal vesicles did not stain for P504S. Five of six (83%) specimens with invasive urothelial carcinoma had 2+ staining and one case had focal staining. We conclude that immunohistochemistry for P504S has potential utility in the diagnosis of prostate cancer, including those treated by hormones and radiation. Circumferential luminal to subluminal and diffuse cytoplasmic staining is the most specific staining pattern for prostatic carcinoma and is almost never associated with benign prostatic tissue. However, a negative P504S immunostain does not automatically rule out prostate cancer, as 18% of cases were negative. Additionally, occasional benign glands, high-grade prostatic intraepithelial neoplasia, atypical adenomatous hyperplasia, and urothelial carcinoma may express P504S. Therefore, we think that P504S is best used only in conjunction with strict light microscopic correlation and preferably with high molecular weight cytokeratin immunostaining.

摘要

P504S是一种最近被描述的前列腺癌特异性基因,它编码一种参与支链脂肪酸β-氧化的蛋白质。最近一项研究表明,在福尔马林固定、石蜡包埋的组织中,P504S基因产物的免疫组化检测是前列腺癌的一种敏感且特异的标志物。我们对大量前列腺和膀胱标本中的P504S蛋白表达进行了详细分析,特别着重于前列腺腺癌特定形态学模式、激素治疗和放疗病例以及浸润性尿路上皮癌中的染色情况。对124例前列腺癌患者的366份前列腺穿刺活检标本、2例无前列腺癌患者的10份活检标本、28份前列腺切除标本(16份具有特定形态学模式、7份激素治疗后标本和5份放疗后标本)、5份浸润性尿路上皮癌膀胱标本以及1例接受激素治疗的前列腺癌合并浸润性尿路上皮癌患者的经尿道切除标本,使用标准热诱导抗原修复和抗生物素蛋白-生物素技术,以1:250稀释度的P504S单克隆抗体进行染色。记录癌组织和良性组织中免疫反应的程度(0,无染色;1+,1%-10%染色;2+,11%-50%染色;3+,≥51%染色)和位置(管腔、管腔下和弥漫性细胞质)。186份前列腺腺癌活检标本中有153份(82%)P504S染色阳性。假增生性、萎缩性、导管性和黏液性前列腺癌染色情况相似,激素或放疗治疗的病例也是如此。在377个良性前列腺组织灶中的81个(21%)有染色,几乎总是局灶性、淡染且非环状的。精囊P504S不染色。6份浸润性尿路上皮癌标本中有5份(83%)为2+染色,1例有局灶性染色。我们得出结论,P504S免疫组化在前列腺癌诊断中具有潜在应用价值,包括那些接受激素和放疗治疗的病例。从管腔到管腔下的环状以及弥漫性细胞质染色是前列腺癌最具特异性染色模式,几乎从不与良性前列腺组织相关。然而,P504S免疫染色阴性并不能自动排除前列腺癌,因为18%的病例为阴性。此外,偶尔良性腺体、高级别前列腺上皮内瘤变、非典型腺瘤样增生和尿路上皮癌可能表达P504S。因此,我们认为P504S最好仅与严格的光学显微镜观察相结合使用,最好同时进行高分子量细胞角蛋白免疫染色。

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