Egloff Ann Marie, Weissfeld Joel, Land Stephanie R, Finn Olivera J
University of Pittsburgh School of Medicine, E1040 Biomedical Science Tower, Pittsburgh, PA 15261, USA.
Ann N Y Acad Sci. 2005 Dec;1062:29-40. doi: 10.1196/annals.1358.005.
The primary aims of this study were to establish a high-throughput assay and analytic procedures that would allow us to assess with accuracy and reproducibility the presence of anti-cyclin B1 antibodies in a large cohort of subjects at-risk for development of lung cancer. The overall goal is to identify factors significantly associated with immune responses against this lung tumor antigen and to evaluate the relationship between anticyclin B1 antibodies and lung cancer risk in a prospective cohort. Successful cancer treatment relies on early detection. The immune system could respond to tumor antigens arising from altered host factors and provide an early readout for cancer presence. This study examines immune responses to the tumor antigen cyclin B1. Lung cancer patients have antibodies against cyclin B1. Unscheduled overexpression of this cell cycle regulator occurs early in tumorigenesis and might be detected by the immune system long before clinical diagnosis of cancer. Antibodies recognizing cyclin B1 were measured using semiautomated ELISAs in sera samples from subjects without detectable lung cancer enrolled in the Pittsburgh Lung Screening Study (PLuSS), a longitudinal study of long-term smokers over age 50. Factors significantly associated with antibody presence were identified using linear regression analysis. We have established a highly reproducible, semiautomated ELISA-based assay for the high-throughput assessment of serum antibody titers. Using this technology and a small subset of PluSS subjects, cyclin B1 antibody levels were found to be high in a small proportion of subjects tested. Regression analysis identified gender as well as age in women smokers to be significant determinants of cyclin B1 antibody levels, association not seen in male subjects. This work represents an important first step toward defining the importance of the presence of anticyclin B1 antibodies in an at-risk population and assessing the predictive value of serum cyclin B1 antibody as relates to lung cancer risk.
本研究的主要目的是建立一种高通量检测方法和分析程序,使我们能够准确且可重复地评估一大群有肺癌发病风险的受试者中抗细胞周期蛋白B1抗体的存在情况。总体目标是确定与针对这种肺肿瘤抗原的免疫反应显著相关的因素,并在前瞻性队列中评估抗细胞周期蛋白B1抗体与肺癌风险之间的关系。成功的癌症治疗依赖于早期检测。免疫系统可以对由宿主因素改变产生的肿瘤抗原做出反应,并为癌症的存在提供早期信号。本研究检测了对肿瘤抗原细胞周期蛋白B1的免疫反应。肺癌患者有抗细胞周期蛋白B1抗体。这种细胞周期调节因子的异常过表达在肿瘤发生早期就会出现,可能早在癌症临床诊断之前就被免疫系统检测到。使用半自动酶联免疫吸附测定法(ELISA)检测了匹兹堡肺癌筛查研究(PLuSS)中未检测出肺癌的受试者血清样本中识别细胞周期蛋白B1的抗体。PLuSS是一项针对50岁以上长期吸烟者的纵向研究。使用线性回归分析确定了与抗体存在显著相关的因素。我们已经建立了一种基于ELISA的高度可重复的半自动检测方法,用于高通量评估血清抗体滴度。使用这项技术和一小部分PLuSS受试者,发现一小部分受试对象的细胞周期蛋白B1抗体水平较高。回归分析确定性别以及女性吸烟者的年龄是细胞周期蛋白B1抗体水平的重要决定因素,而在男性受试者中未发现这种关联。这项工作是确定抗细胞周期蛋白B1抗体在高危人群中存在的重要性以及评估血清细胞周期蛋白B1抗体与肺癌风险相关的预测价值的重要第一步。