Pereira-Faca Sandra R, Kuick Rork, Puravs Eric, Zhang Qing, Krasnoselsky Alexei L, Phanstiel Douglas, Qiu Ji, Misek David E, Hinderer Robert, Tammemagi Martin, Landi Maria Teresa, Caporaso Neil, Pfeiffer Ruth, Edelstein Cim, Goodman Gary, Barnett Matt, Thornquist Mark, Brenner Dean, Hanash Samir M
Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.
Cancer Res. 2007 Dec 15;67(24):12000-6. doi: 10.1158/0008-5472.CAN-07-2913.
We have implemented a strategy to identify tumor antigens that induce a humoral immune response in lung cancer based on the analysis of tumor cell proteins. Chromatographically fractionated protein extracts from three lung cancer cell lines were subjected to Western blotting and hybridization with individual sera to determine serum antibody binding. Two sets of sera were initially investigated. One set consisted of sera from 19 newly diagnosed subjects with lung adenocarcinoma and 19 matched controls. A second independent set consisted of sera from 26 newly diagnosed subjects with lung adenocarcinoma and 24 controls matched for age, gender, and smoking history. One protein that exhibited significant reactivity with both sets of cancer sera (P = 0.0008) was confidently identified by mass spectrometry as 14-3-3 theta. Remarkably, significant autoantibody reactivity against 14-3-3 theta was also observed in an analysis of a third set consisting of 18 prediagnostic lung cancer sera collected as part of the Beta-Carotene and Retinol Efficacy Trial cohort study, relative to 19 matched controls (P = 0.0042). A receiver operating characteristic curve constructed with a panel of three proteins consisting of 14-3-3 theta identified in this study, plus annexin 1 and protein gene product 9.5 proteins previously identified as associated with autoantibodies in lung cancer, gave a sensitivity of 55% at 95% specificity (area under the curve, 0.838) in discriminating lung cancer at the preclinical stage from matched controls.
基于对肿瘤细胞蛋白质的分析,我们实施了一项策略来鉴定可在肺癌中诱导体液免疫反应的肿瘤抗原。从三种肺癌细胞系中通过色谱法分离得到的蛋白质提取物,进行了蛋白质印迹分析,并与个体血清杂交以确定血清抗体结合情况。最初研究了两组血清。一组由19名新诊断的肺腺癌患者的血清和19名匹配的对照血清组成。第二组独立血清由26名新诊断的肺腺癌患者的血清和24名年龄、性别及吸烟史相匹配的对照血清组成。通过质谱法确切鉴定出一种与两组癌症血清均表现出显著反应性的蛋白质(P = 0.0008)为14-3-3θ。值得注意的是,在对作为β-胡萝卜素和视黄醇功效试验队列研究一部分收集的18份肺癌诊断前血清组成的第三组进行分析时,相对于19名匹配对照,也观察到了针对14-3-3θ的显著自身抗体反应性(P = 0.0042)。利用本研究中鉴定出的14-3-3θ以及先前确定与肺癌自身抗体相关的膜联蛋白1和蛋白基因产物9.5这三种蛋白质组成的蛋白组构建的受试者工作特征曲线,在区分临床前阶段的肺癌与匹配对照时,在95%特异性下灵敏度为55%(曲线下面积为0.838)。