cpz_:一种高度敏感的肝细胞癌和肝内胆管癌鉴别诊断标志物,特别是在低分化肝细胞癌中。

IF 4.5 1区 医学 Q1 PATHOLOGY
Minying Deng, Rongkui Luo, Lingli Chen, Huimei Wang, Wen Huang, Qi Song, Dongxian Jiang, Lei Xu, Jieakesu Su, Chen Xu, Yingyong Hou
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引用次数: 0

摘要

羧基肽酶Z (CPZ)是一种新发现的金属肽酶家族成员,主要在大鼠中报道;然而,其在正常人体组织中的分布及在肿瘤组织中的表达特征尚不清楚。本研究利用组织微阵列(tissue microarray, TMA)高通量、大批量生产技术对CPZ进行免疫组化染色,首次描绘CPZ在正常组织及全身各种肿瘤中的分布和表达,探讨其潜在的病理价值。CPZ在正常肝细胞、胰岛和胆囊上皮中均有不同程度的细胞质阳性表达,在其他正常组织中未见表达。CPZ在肝细胞癌(HCC)、肝内cholangiocarcinoma (ICC)、转移性肝肿瘤和正常肝组织中的阳性表达率分别为90.8 %(109/120)、27.7 %(13/47)、0%(0/22)和100%(81/81)。CPZ、精氨酸酶-1 (Arg-1)和hepatocyte石蜡抗原-1 (Hep Par-1) 3种标志物阳性诊断HCC的敏感性和特异性分别为96.7%(116/120)和65.2%(45/69)。3项指标均阳性诊断HCC的敏感性和特异性分别为70.8%(85/120)和100%(69/69)。CPZ和Arg-1同时阳性诊断HCC的敏感性和特异性分别为79.2%(95/120)和95.7%(66/69)。CPZ和Hep Par-1阳性诊断HCC的敏感性和特异性分别为76.7%(92/120)和97.1%(67/69)。Arg-1和Hep Par-1阳性诊断HCC的敏感性和特异性分别为72.5%(87/120)和98.6%(68/69)。ROC曲线显示,CPZ、Arg-1、Hep Par-1联合检测对HCC的诊断价值最佳(AUC=0.939, P = 0.05)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CPZ: A Highly Sensitive Diagnostic Biomarker for the Differentiation Between Hepatocellular Carcinoma and Intrahepatic Cholangiocarcinoma, Particularly in Poorly Differentiated Hepatocellular Carcinoma.

Carboxypeptidase Z (CPZ) is a newly identified member of the metallopeptidase family, primarily reported in rats; however, its distribution in normal human tissues and expression characteristics in tumor tissues remain unclear. This study uses high-throughput and mass production technology for tissue microarray (TMA) to perform immunohistochemical staining of CPZ, for the first time delineating its distribution and expression in normal tissues and various tumors throughout the body, to discuss its potential pathologic value. CPZ exhibited varying degrees of cytoplasmic positive expression in the normal hepatocytes, pancreatic islets, and gallbladder epithelium, with no expression observed in other normal tissues. The positive expression rates of CPZ in hepatocellular carcinoma (HCC), intrahepatic cholangiocarcinoma (ICC), metastatic liver tumors, and normal liver tissue were 90.8% (109/120), 27.7% (13/47), 0% (0/22), and 100% (81/81), respectively. The sensitivity and specificity for diagnosing HCC with any of the 3 markers (CPZ, arginase-1 (Arg-1), and hepatocyte paraffin antigen-1 (Hep Par-1)) positive were 96.7% (116/120) and 65.2% (45/69), respectively. The sensitivity and specificity for diagnosing HCC with all 3 markers positive were 70.8% (85/120) and 100% (69/69), respectively. The sensitivity and specificity for diagnosing HCC with both CPZ and Arg-1 positive were 79.2% (95/120) and 95.7% (66/69), respectively. The sensitivity and specificity for diagnosing HCC with both CPZ and Hep Par-1 positive were 76.7% (92/120) and 97.1% (67/69), respectively. The sensitivity and specificity for diagnosing HCC with both Arg-1 and Hep Par-1 positive were 72.5% (87/120) and 98.6% (68/69), respectively. The ROC curve indicated that the combined detection of CPZ, Arg-1, and Hep Par-1 had the best diagnostic value for HCC (AUC=0.939, P<0.001). However, for individual detection, CPZ had the highest AUC value among the 3 markers (AUC=0.908, P<0.001). CPZ was not observed to be positive in the majority of 897 cases of solid tumors. Utilizing the TMA repository, we propose for the first time that CPZ may serve as a useful adjunctive tool for the diagnosis or differential diagnosis of HCC in routine surgical pathology practice. CPZ shows a trend of superiority over Arg-1 and Hep Par-1, particularly in poorly differentiated HCC.

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来源期刊
CiteScore
10.30
自引率
5.40%
发文量
295
审稿时长
1 months
期刊介绍: The American Journal of Surgical Pathology has achieved worldwide recognition for its outstanding coverage of the state of the art in human surgical pathology. In each monthly issue, experts present original articles, review articles, detailed case reports, and special features, enhanced by superb illustrations. Coverage encompasses technical methods, diagnostic aids, and frozen-section diagnosis, in addition to detailed pathologic studies of a wide range of disease entities. Official Journal of The Arthur Purdy Stout Society of Surgical Pathologists and The Gastrointestinal Pathology Society.
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