Yamanaka Y, Ishida H, Okada K, Nemoto N
Department of Urology, Nihon University School of Medicine.
Nihon Hinyokika Gakkai Zasshi. 2001 Jul;92(5):545-53. doi: 10.5980/jpnjurol1989.92.545.
We performed immunohistochemical studies of the prostatic epithelium using three different anti-cytokeratin monoclonal antibodies (35 beta-H11, RCK108, and 34 beta-E12), and also investigated the immunoreactivity of various prostatic lesions with basal cell specific anti-cytokeratin antibody (34 beta-E12).
One hundred and thirty one prostatic specimens were obtained at surgery or biopsy. H-E stained sections were available for review in all cases. They were classified according to histopathology; benign prostatic hyperplasia (BPH), prostatic cancer (PCA), atrophic acini, atypical adenomatous hyperplasia (AAH), and prostatic intraepithelial neoplasia (PIN). ABC or LSAB method was utilized for immunohistochemical staining with 3 anti-cytokeratin monoclonal antibodies.
35 beta-H11 was mainly stained in the luminal cells and RCK108 was stained both in the luminal and the basal cells in BPH. 35 beta-H11 showed highly positive staining in the prostatic cancer regardless of degree of differentiation. RCK108 tended to be less stained in the prostatic cancer cells with lower grades of tumor differentiation compared to those with higher grades. 34 beta-E12 was stained only in the basal cells, but neither in the normal luminal cells nor the cancer cells. Using 34 beta-E 12, basal cells were positively stained in most of the cases with BPH, while not in PCA. Atrophic acini and AAH was stained with 34 beta-E12 as positively as BPH. Basal cells were discontinuously or negatively stained in many cases with high-grade PIN.
The luminal cells in BPH were highly positively stained using 35 beta-H11 or RCK108. RCK108 tended to be less stained in the prostatic cancer cells with lower grades of tumor differentiation. Positive staining of 34 beta-E12 strongly suggested a benign lesion, therefore immunohistochemistry using this antibody would be useful as an aid for pathological diagnosis.
我们使用三种不同的抗细胞角蛋白单克隆抗体(35β-H11、RCK108和34β-E12)对前列腺上皮进行免疫组织化学研究,并使用基底细胞特异性抗细胞角蛋白抗体(34β-E12)研究各种前列腺病变的免疫反应性。
通过手术或活检获取131份前列腺标本。所有病例均有苏木精-伊红(H-E)染色切片可供复查。根据组织病理学将其分类为:良性前列腺增生(BPH)、前列腺癌(PCA)、萎缩性腺泡、非典型腺瘤样增生(AAH)和前列腺上皮内瘤变(PIN)。采用ABC或LSAB法用3种抗细胞角蛋白单克隆抗体进行免疫组织化学染色。
在良性前列腺增生中,35β-H11主要染色于管腔细胞,RCK108在管腔细胞和基底细胞中均有染色。无论分化程度如何,35β-H11在前列腺癌中均显示高度阳性染色。与高分化的前列腺癌细胞相比,低分化的前列腺癌细胞中RCK108的染色往往较少。34β-E12仅在基底细胞中染色,在正常管腔细胞和癌细胞中均不染色。使用34β-E12时,大多数良性前列腺增生病例的基底细胞呈阳性染色,而前列腺癌病例则不然。萎缩性腺泡和非典型腺瘤样增生与良性前列腺增生一样,34β-E12染色呈阳性。在许多高级别前列腺上皮内瘤变病例中,基底细胞呈间断性或阴性染色。
使用35β-H11或RCK108时,良性前列腺增生中的管腔细胞呈高度阳性染色。低分化的前列腺癌细胞中RCK108的染色往往较少。34β-E12的阳性染色强烈提示为良性病变,因此使用该抗体进行免疫组织化学检查有助于病理诊断。