Wang Y, Hou M Y, Fu Y, Meng K, Wu H Y, Chen J, Xu Y M, Shi J, Fan X S
Department of Pathology, the Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing 210008, China.
Zhonghua Bing Li Xue Za Zhi. 2023 Apr 8;52(4):358-363. doi: 10.3760/cma.j.cn112151-20220711-00594.
To investigate the expression of glycoprotein non metastatic melanoma protein B (GPNMB) in renal eosinophilic tumors and to compare the value of GPNMB with CK20, CK7 and CD117 in the differential diagnosis of renal eosinophilic tumors. Traditional renal tumor eosinophil subtypes, including 22 cases of renal clear cell carcinoma eosinophil subtype (e-ccRCC), 19 cases of renal papillary cell carcinoma eosinophil subtype (e-papRCC), 17 cases of renal chromophobe cell carcinoma eosinophil subtype (e-chRCC), 12 cases of renal oncocytoma (RO) and emerging renal tumor types with eosinophil characteristics [3 cases of eosinophilic solid cystic renal cell carcinoma (ESC RCC), 3 cases of renal low-grade eosinophil tumor (LOT), 4 cases of fumarate hydratase-deficient renal cell carcinoma (FH-dRCC) and 5 cases of renal epithelioid angiomyolipoma (E-AML)], were collected at the Affiliated Drum Tower Hospital of Nanjing University Medical School from January 2017 to March 2022. The expression of GPNMB, CK20, CK7 and CD117 was detected by immunohistochemistry and statistically analyzed. GPNMB was expressed in all emerging renal tumor types with eosinophil characteristics (ESC RCC, LOT, FH-dRCC) and E-AML, while the expression rates in traditional renal eosinophil subtypes e-papRCC, e-chRCC, e-ccRCC and RO were very low or zero (1/19, 1/17, 0/22 and 0/12, respectively); the expression rate of CK7 in LOT (3/3), e-chRCC (15/17), e-ccRCC (4/22), e-papRCC (2/19), ESC RCC (0/3), RO (4/12), E-AML(1/5), and FH-dRCC (2/4) variedly; the expression of CK20 was different in ESC RCC (3/3), LOT(3/3), e-chRCC(1/17), RO(9/12), e-papRCC(4/19), FH-dRCC(1/4), e-ccRCC(0/22) and E-AML(0/5), and so did that of CD117 in e-ccRCC(2/22), e-papRCC(1/19), e-chRCC(16/17), RO(10/12), ESC RCC(0/3), LOT(1/3), E-AML(2/5) and FH-dRCC(1/4). GPNMB had 100% sensitivity and 97.1% specificity in distinguishing E-AML and emerging renal tumor types (such as ESC RCC, LOT, FH-dRCC) from traditional renal tumor types (such as e-ccRCC, e-papRCC, e-chRCC, RO),respectively. Compared with CK7, CK20 and CD117 antibodies, GPNMB was more effective in the differential diagnosis (<0.05). As a new renal tumor marker, GPNMB can effectively distinguish E-AML and emerging renal tumor types with eosinophil characteristics such as ESC RCC, LOT, FH-dRCC from traditional renal tumor eosinophil subtypes such as e-ccRCC, e-papRCC, e-chRCC and RO, which is helpful for the differential diagnosis of renal eosinophilic tumors.
探讨糖蛋白非转移性黑色素瘤蛋白B(GPNMB)在肾嗜酸性肿瘤中的表达,并比较GPNMB与细胞角蛋白20(CK20)、细胞角蛋白7(CK7)和CD117在肾嗜酸性肿瘤鉴别诊断中的价值。收集南京大学医学院附属鼓楼医院2017年1月至2022年3月的传统肾肿瘤嗜酸性粒细胞亚型,包括22例肾透明细胞癌嗜酸性粒细胞亚型(e-ccRCC)、19例肾乳头状细胞癌嗜酸性粒细胞亚型(e-papRCC)、17例肾嫌色细胞癌嗜酸性粒细胞亚型(e-chRCC)、12例肾嗜酸细胞瘤(RO)以及具有嗜酸性特征的新型肾肿瘤类型[3例嗜酸性实性囊性肾细胞癌(ESC RCC)、3例肾低度嗜酸性肿瘤(LOT)、4例富马酸水合酶缺陷型肾细胞癌(FH-dRCC)和5例肾上皮样血管平滑肌脂肪瘤(E-AML)]。采用免疫组织化学法检测GPNMB、CK20、CK7和CD117的表达,并进行统计学分析。GPNMB在所有具有嗜酸性特征的新型肾肿瘤类型(ESC RCC、LOT、FH-dRCC)和E-AML中均有表达,而在传统肾嗜酸性粒细胞亚型e-papRCC、e-chRCC、e-ccRCC和RO中的表达率极低或为零(分别为1/19、1/17、0/22和0/12);CK7在LOT(3/3)、e-chRCC(15/17)、e-ccRCC(4/22)、e-papRCC(2/19)、ESC RCC(0/3)、RO(4/12)、E-AML(1/5)和FH-dRCC(2/4)中的表达各不相同;CK20在ESC RCC(3/3)、LOT(3/3)、e-chRCC(1/17)、RO(9/12)、e-papRCC(4/19)、FH-dRCC(1/4)、e-ccRCC(0/22)和E-AML(0/5)中的表达不同,CD117在e-ccRCC(2/22)、e-papRCC(1/19)、e-chRCC(16/17)、RO(10/12)、ESC RCC(0/3)、LOT(1/3)、E-AML(2/5)和FH-dRCC(1/4)中的表达也不同。GPNMB在区分E-AML和新型肾肿瘤类型(如ESC RCC、LOT、FH-dRCC)与传统肾肿瘤类型(如e-ccRCC、e-papRCC、e-chRCC、RO)方面分别具有100%的敏感性和97.1%的特异性。与CK7、CK20和CD117抗体相比,GPNMB在鉴别诊断中更有效(<0.05)。作为一种新型肾肿瘤标志物,GPNMB可有效区分E-AML和具有嗜酸性特征的新型肾肿瘤类型,如ESC RCC、LOT、FH-dRCC与传统肾肿瘤嗜酸性粒细胞亚型,如e-ccRCC、e-papRCC、e-chRCC和RO,这有助于肾嗜酸性肿瘤的鉴别诊断。