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用于筛选乙肝病毒诱导的肝细胞癌血清标志物的表面增强激光解吸电离飞行时间质谱蛋白质芯片技术

SELDI-TOF MS proteinchip technology for screening of serum markers of HBV-induced hepatocellular carcinoma.

作者信息

Geng X, Wang F, Li Y G, Zhu G P, Zhang W M

机构信息

Basic Medical School, Tianjin Medical University, Tianjin, China.

出版信息

J Exp Clin Cancer Res. 2007 Dec;26(4):505-8.

Abstract

The incidence of hepatocellular carcinoma (HCC) is highest among primary liver cancer. HBV and HBV-induced liver cirrhosis may lead to HCC (1). At present, it is difficult to diagnose HCC at early stage or to differentiate HCC. Therefore, it is much needed to explore and develop a simple, rapid diagnostic method, which has higher sensitivity and specificity for HCC at early stage (2, 3). Surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF MS) is a novel non-electrophoresis-based proteomic technology. SELDI offers the advantages of rapid and simple examination as well as high specificity and sensitivity (4, 5). To our knowledge,there has been little study reported using SELDI-TOF-MS technology to investigate HCC. In this study, 25 cases of HCC patients not receiving any therapy, 25 cases receiving the interposition chemotherapy and 50 cases of the healthy people were tested by Weak cationic exchange (WCX2) protein chip and SELDI-TOF-MS. The differentially expressed peptides or proteins were analyzed by BioMarker Wizard software. At the different M/Z value range, seven peptides/ proteins were obviously different among these three groups. Four peptides including 6489.48Da, 6662.34Da, 8593.75Da and 8720.23Da were up-regulated in healthy controls, two including 7777.27Da and 9250.00Da were up-regulated in the patients with HCC without receiving any therapy and one protein of 16200.17Da was up-regulated in the patients with HCC receiving the interposition chemotherapy. Using Biomarker Pattern software, one pattern including two peptides (7777.27Da, 9250.00Da) can separate HCC without receiving any therapy from normal controls. This diagnosis pattern gave the much-improved sensitivity of 92% and the specificity of 100%. Through searching protein database, these seven peptides or proteins were identified as possible Galanin related peptide, Pro-neuregulin-4 protein, small inducible cytokine A15 precursor, 9 kDa protein, CSL-zincfinger protein 1, mitochondrial hinge protein, actin related protein, respectively. Using SELDI-TOF MS, the method of sieving the tumor markers from HCC becomes quick and valid. These differentially expressed peptides or proteins could be biomarkers of HCC in the serum and drug targets for treating HCC.

摘要

肝细胞癌(HCC)在原发性肝癌中发病率最高。乙肝病毒(HBV)及HBV诱导的肝硬化可导致HCC(1)。目前,HCC的早期诊断及鉴别诊断仍存在困难。因此,迫切需要探索并开发一种简便、快速的诊断方法,该方法对早期HCC具有更高的敏感性和特异性(2,3)。表面增强激光解吸/电离飞行时间质谱(SELDI-TOF MS)是一种新型的基于非电泳的蛋白质组学技术。SELDI具有检测快速简便、特异性和敏感性高的优点(4,5)。据我们所知,很少有研究报道使用SELDI-TOF-MS技术研究HCC。本研究采用弱阳离子交换(WCX2)蛋白质芯片和SELDI-TOF-MS对25例未接受任何治疗的HCC患者、25例接受介入化疗的患者及50例健康人进行检测。通过BioMarker Wizard软件分析差异表达的肽段或蛋白质。在不同的质荷比(M/Z)值范围内,三组之间有7种肽段/蛋白质存在明显差异。其中,6489.48Da、6662.34Da、8593.75Da和8720.23Da这4种肽段在健康对照组中上调,7777.27Da和9250.00Da这2种在未接受任何治疗的HCC患者中上调,16200.17Da的一种蛋白质在接受介入化疗的HCC患者中上调。使用Biomarker Pattern软件,一种包含2种肽段(7777.27Da、9250.00Da)的模式可将未接受任何治疗的HCC与正常对照区分开来。该诊断模式的敏感性提高到92%,特异性为100%。通过检索蛋白质数据库,这7种肽段或蛋白质分别被鉴定为可能的甘丙肽相关肽、前神经调节蛋白-4、小诱导细胞因子A15前体、9 kDa蛋白、CSL锌指蛋白1、线粒体铰链蛋白、肌动蛋白相关蛋白。利用SELDI-TOF MS从HCC中筛选肿瘤标志物的方法快速有效。这些差异表达的肽段或蛋白质可能成为HCC血清中的生物标志物及治疗HCC的药物靶点。

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