Cancer Biomarkers Development Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 305-806, Korea.
BMB Rep. 2012 Dec;45(12):677-85. doi: 10.5483/bmbrep.2012.45.12.236.
In the process of tumorigenesis, normal cells are remodeled to cancer cells and protein expression patterns are changed to those of tumor cells. A newly formed tumor microenvironment elicits the immune system and, as a result, a humoral immune response takes place. Although the tumor antigens are undetectable in sera at the early stage of tumorigenesis, the nature of an antibody amplification response to antigens makes tumor-associated autoantibodies as promising early biomarkers in cancer diagnosis. Moreover, the recent development of proteomic techniques that make neo-epitopes of tumor-associated autoantigens discovered concomitantly has opened a new area of 'immuno-proteomics', which presents tumor-associated autoantibody signatures and confers information to redefine the process of tumorigenesis. In this article, the strategies recently used to identify and validate serum autoantibodies are outlined and tumor-associated antigens suggested until now as diagnostic/prognostic biomarkers in various tumor types are reviewed. Also, the meaning of autoantibody signatures and their clinical utility in personalized medicine are discussed.
在肿瘤发生过程中,正常细胞被重塑为癌细胞,蛋白表达模式发生改变,成为肿瘤细胞的特征。新形成的肿瘤微环境会引发免疫系统,从而引发体液免疫反应。尽管在肿瘤发生的早期阶段,血清中的肿瘤抗原无法检测到,但针对抗原的抗体扩增反应的性质使得肿瘤相关自身抗体成为癌症诊断中有前途的早期生物标志物。此外,最近蛋白质组学技术的发展使得肿瘤相关自身抗原的新表位同时被发现,开辟了“免疫蛋白质组学”的新领域,它呈现了肿瘤相关自身抗体的特征,并提供了信息来重新定义肿瘤发生的过程。在本文中,概述了最近用于鉴定和验证血清自身抗体的策略,并回顾了迄今为止在各种肿瘤类型中作为诊断/预后生物标志物的肿瘤相关抗原。此外,还讨论了自身抗体特征的意义及其在个性化医学中的临床应用。