Qiu Ji, Choi Gina, Li Lin, Wang Hong, Pitteri Sharon J, Pereira-Faca Sandra R, Krasnoselsky Alexei L, Randolph Timothy W, Omenn Gilbert S, Edelstein Cim, Barnett Matt J, Thornquist Mark D, Goodman Gary E, Brenner Dean E, Feng Ziding, Hanash Samir M
Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
J Clin Oncol. 2008 Nov 1;26(31):5060-6. doi: 10.1200/JCO.2008.16.2388. Epub 2008 Sep 15.
We have implemented a high throughput platform for quantitative analysis of serum autoantibodies, which we have applied to lung cancer for discovery of novel antigens and for validation in prediagnostic sera of autoantibodies to antigens previously defined based on analysis of sera collected at the time of diagnosis.
Proteins from human lung adenocarcinoma cell line A549 lysates were subjected to extensive fractionation. The resulting 1,824 fractions were spotted in duplicate on nitrocellulose-coated slides. The microarrays produced were used in a blinded validation study to determine whether annexin I, PGP9.5, and 14-3-3 theta antigens previously found to be targets of autoantibodies in newly diagnosed patients with lung cancer are associated with autoantibodies in sera collected at the presymptomatic stage and to determine whether additional antigens may be identified in prediagnostic sera. Individual sera collected from 85 patients within 1 year before a diagnosis of lung cancer and 85 matched controls from the Carotene and Retinol Efficacy Trial (CARET) cohort were hybridized to individual microarrays.
We present evidence for the occurrence in lung cancer sera of autoantibodies to annexin I, 14-3-3 theta, and a novel lung cancer antigen, LAMR1, which precede onset of symptoms and diagnosis.
Our findings suggest potential utility of an approach to diagnosis of lung cancer before onset of symptoms that includes screening for autoantibodies to defined antigens.
我们已实施了一个用于血清自身抗体定量分析的高通量平台,并将其应用于肺癌研究,以发现新的抗原,并在基于诊断时采集的血清分析预先确定的抗原的自身抗体的预诊断血清中进行验证。
对人肺腺癌细胞系A549裂解物中的蛋白质进行广泛分级分离。将得到的1824个级分一式两份点样于硝酸纤维素包被的载玻片上。所制备的微阵列用于一项盲法验证研究,以确定先前在新诊断的肺癌患者中发现的作为自身抗体靶标的膜联蛋白I、PGP9.5和14-3-3θ抗原是否与症状前期采集的血清中的自身抗体相关,并确定是否可在预诊断血清中鉴定出其他抗原。将从85例肺癌诊断前1年内采集的个体血清以及来自胡萝卜素和视黄醇功效试验(CARET)队列的85例匹配对照的血清与个体微阵列进行杂交。
我们提供了证据,证明在肺癌血清中存在针对膜联蛋白I、14-3-3θ和一种新的肺癌抗原LAMR1的自身抗体,这些自身抗体在症状出现和诊断之前就已存在。
我们的研究结果表明,一种在症状出现前诊断肺癌的方法具有潜在实用性,该方法包括筛查针对特定抗原的自身抗体。