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Uroplakin II Is a More Sensitive Immunohistochemical Marker Than Uroplakin III in Urothelial Carcinoma and Its Variants.

与尿路上皮分化有关的特异糖蛋白III相比,尿路上皮分化有关的特异糖蛋白II对尿路上皮癌及其变异型是一种更敏感的免疫组化标记。

Li W,Liang Y,Deavers MT,Kamat AM,Matin SF,Dinney CP,Czerniak B,Guo CC

Abstract

Uroplakin (UP) II and UPIII are highly specific immunohistochemical markers for urothelial differentiation. Here we studied the sensitivity of UPII and UPIII in conventional and variant urothelial carcinomas (UCs).
Immunohistochemical staining for UPII and UPIII was performed on tissue microarray slides, including 105 conventional bladder UCs (BUCs), 90 upper urinary tract UCs (UUTUCs), and 47 micropapillary, 16 plasmacytoid, 22 small cell carcinoma, and 41 sarcomatoid UC variants.
UPII expression was significantly higher than UPIII expression in conventional BUC (44% vs 17%, P < .001) and UUTUC (67% vs 46%, P = .045). UPIII expression was significantly higher in UUTUC than in BUC (P < .001). In UC variants, UPII expression was significantly higher than UPIII expression in micropapillary (91% vs 25%, P < .001), plasmacytoid (63% vs 6%, P < .001), and sarcomatoid (29% vs 5%, P = .032) variants. Only rare cases of the small cell carcinoma variant had focal UPII and UPIII expression. Compared with conventional UC, the sarcomatoid variant had significantly lower UPII expression, whereas the micropapillary variant had significantly higher UPII expression (P < .001).
UPII demonstrates a significantly higher sensitivity than UPIII in conventional and variant UCs. Thus, UPII is a more valuable marker than UPIII in immunohistochemical analyses for confirming the urothelial origin of carcinomas.

摘要

尿路上皮分化有关的特异糖蛋白(UP)II和UPIII是对尿路上皮分化具有高度特异性的免疫组化标记。我们研究了UPII和UPIII在普通型和变异型尿路上皮癌(UC)的中敏感性。
对组织芯片样本进行UPII和UPIII免疫组化染色,其中包括105例普通型膀胱UC(BUC),90例上尿路UC(UUTUC),和47例微乳头型,16例浆细胞样型,22例小细胞癌和41例肉瘤样型UC。
在普通型BUC和UUTUC中,UPII表达显着高于UPIII表达(在普通型BUC中,44%比17%,P<0.001;< span="">在UUTUC中,67%比46%,P =0.045)。在UUTUC中UPIII表达显着高于在BUC中(P<0.001)。在UC的变异型里,微乳头型、浆细胞样型和肉瘤样型的UPII表达显着高于UPIII表达(在微乳头型中,91%比25%,P <0.001;在浆细胞样型中,63%比6%,P <0.001;在肉瘤样型中,29%比5%, P =.032)。而小细胞癌变异型只有极少数病例有局灶UPII和UPIII表达。与普通型UC相比,肉瘤样型的UPII表达显着降低,而微乳头型的UPII表达显着增高(P<0.001)。
研究表明,UPII在常规和变异UC中比UPIII具有显着更高的灵敏度。因此,与UPIII相比,UPII对确定尿路上皮起源的癌是一种更有价值的免疫组化标记。

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