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使用表面增强激光解吸/电离飞行时间质谱法鉴定肝细胞癌的血清生物标志物。

Identifying serological biomarkers of hepatocellular carcinoma using surface-enhanced laser desorption/ionization-time-of-flight mass spectroscopy.

作者信息

Wu Fei-Xiang, Wang Qi, Zhang Zhi-Ming, Huang Shang, Yuan Wei-Ping, Liu Jian-Yong, Ban Ke-Chen, Zhao Yin-Nong

机构信息

Department of Hepatobiliary Surgery, Tumor Hospital of Guangxi Medical University, Nanning, Guangxi 530021, PR China.

出版信息

Cancer Lett. 2009 Jul 8;279(2):163-70. doi: 10.1016/j.canlet.2009.01.034. Epub 2009 Mar 5.

Abstract

Lack of sensitive and specific biomarkers is a major reason for the high rate of hepatocellular carcinoma (HCC) related mortality. The aim of this study was to use surface-enhanced laser desorption/ionization-time-of-flight mass spectroscopy (SELDI-TOF-MS) technology to identify potential protein patterns specific for HCC. Eighty-one patients with hepatitis B-related HCC and 80 healthy controls were randomly divided into a training set (48 HCC, 47 controls) and a testing set (33 HCC, 33 controls). Serum proteomic profiles were measured using SELDI-TOF-MS. A classification tree was established by Biomarker Pattern Software. Candidate biomarkers were separated by HPLC and identified by MALDI-MS/MS and database searching. Forty-eight HCC cases, 54 liver cirrhosis cases and 42 healthy people were clinically validated using candidate biomarkers by SELDI-Immunoassay. Two up-regulated protein peaks were automatically chosen as a classification tree in the training set. These biomarkers were identified as thrombin light chain and growth related oncogene-alpha (GRO-alpha). The sensitivity and specificity of this classification tree were 89.6%. The multivariate model using the two biomarkers and AFP resulted in a sensitivity of 91.7% and specificity of 92.7%, which was significantly better than that of alpha-fetoprotein alone. We conclude that thrombin light chain and GRO-alpha are potential biomarkers of HCC.

摘要

缺乏敏感且特异的生物标志物是肝细胞癌(HCC)相关死亡率居高不下的主要原因。本研究旨在运用表面增强激光解吸/电离飞行时间质谱(SELDI-TOF-MS)技术来识别HCC特异的潜在蛋白质模式。81例乙型肝炎相关HCC患者和80例健康对照被随机分为训练集(48例HCC,47例对照)和测试集(33例HCC,33例对照)。采用SELDI-TOF-MS测定血清蛋白质组图谱。通过生物标志物模式软件建立分类树。候选生物标志物经高效液相色谱分离,基质辅助激光解吸电离串联质谱(MALDI-MS/MS)及数据库检索鉴定。采用候选生物标志物通过SELDI免疫分析对48例HCC病例、54例肝硬化病例和42例健康人进行临床验证。在训练集中自动选择两个上调的蛋白质峰作为分类树。这些生物标志物被鉴定为凝血酶轻链和生长相关癌基因α(GRO-α)。该分类树的敏感性和特异性为89.6%。使用这两种生物标志物和甲胎蛋白的多变量模型的敏感性为91.7%,特异性为92.7%,显著优于单独使用甲胎蛋白。我们得出结论,凝血酶轻链和GRO-α是HCC的潜在生物标志物。

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