首页> 外文期刊>Hepatitis Monthly >DEVELOPMENT OF A CHEMILUMINESCENCE IMMUNOASSAY FOR SERUM YB-1 AND ITS CLINICAL APPLICATION AS A POTENTIAL DIAGNOSTIC MARKER FOR HEPATOCELLULAR CARCINOMA
【24h】

DEVELOPMENT OF A CHEMILUMINESCENCE IMMUNOASSAY FOR SERUM YB-1 AND ITS CLINICAL APPLICATION AS A POTENTIAL DIAGNOSTIC MARKER FOR HEPATOCELLULAR CARCINOMA

机译:血清YB-1的化学发光免疫分析方法的开发及其在肝细胞癌潜在诊断方面的临床应用

获取原文
           

摘要

Background: Y-box binding protein 1 (YB-1) overexpression has been shown in various tumor cells including hepatocellular carcinoma (HCC), moreover, this protein can be actively secreted.Objectives: The aim of this study was to establish a method to quantify serum YB-1 and evaluate its clinical application in the clinical diagnosis of HCC.Patients and Methods: Recombinant YB-1 and two populations of its antibodies were prepared. A monoclonal antibody was specific to the N-terminus of YB-1 amino acids 134-160, and another was a polyclonal antibody. A sandwich-type chemiluminescence immunoassay (CLIA) was developed and evaluated. Levels of YB-1 and alpha fetoprotein (AFP) in serum samples from 105 HCC patients, 25 hepatitis B virus patients, 25 cirrhosis patients, and 50 healthy donors were detected using the established method and an AFP electro chemiluminescence kit.Results: The developed method was linear to 150 m g/L of YB-1 with a minimum detection limit of 0.01 m g/L. The average recoveries were between 93.9% and 109.0%. The mean intra- and inter-assay coefficients of variation (CVs) were 4.0-4.8% and 8.2-10.2%, respectively. The relationship between the concentration of diluted YB-1 and the dilution ratios gave a good linear correlation coefficient of 0.9986. The YB-1 concentration was increased in serum of HCC patients (33.0±23.39 m g/L) compared to healthy individuals (13.2±5.29 m g/L, PConclusions: The established method has an acceptable performance in quantifying YB-1. In addition, serum YB-1 may aid in the diagnosis of HCC.
机译:背景:Y-box结合蛋白1(YB-1)的表达已在包括肝细胞癌(HCC)在内的各种肿瘤细胞中表达,而且该蛋白可以被主动分泌。目的:本研究的目的是建立一种方法定量检测血清YB-1,并评价其在肝癌临床诊断中的临床应用。病人与方法:制备重组YB-1及其两个抗体群。单克隆抗体对YB-1氨基酸134-160的N端具有特异性,另一个是多克隆抗体。开发并评估了夹心型化学发光免疫分析法(CLIA)。使用建立的方法和AFP电化学发光试剂盒检测了105例HCC患者,25例乙型肝炎病毒患者,25例肝硬化患者和50例健康供体的血清中YB-1和甲胎蛋白(AFP)的水平。该方法与150 mg / L的YB-1呈线性关系,最低检出限为0.01 mg / L。平均回收率在93.9%至109.0%之间。批内和批间平均变异系数(CVs)分别为4.0-4.8%和8.2-10.2%。稀释的YB-1的浓度与稀释比之间的关系给出了良好的线性相关系数0.9986。与健康人(13.2±5.29 mg / L)相比,HCC患者血清中的YB-1浓度增加(33.0±23.39 mg / L),PConclusions:该建立的方法在定量YB-1方面具有可接受的性能。血清YB-1可能有助于肝癌的诊断。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号