Zhang Jian-Ying
Department of Biological Sciences, The University of Texas at El Paso, 500 West University Avenue, El Paso, Texas 79968, USA.
Cancer Detect Prev. 2004;28(2):114-8. doi: 10.1016/j.cdp.2003.12.006.
Cancer sera contain antibodies which react with a unique group of autologous cellular antigens called tumor-associated antigens (TAAs). Cancer has long been recognized as a multi-step process which involves not only genetic changes conferring growth advantage but also factors which disrupt regulation of growth and differentiation. It is possible that some of these factors could be identified and their functions evaluated with the aid of autoantibodies arising during tumorigenesis. The multi-factorial and multi-step nature in the molecular pathogenesis of human cancers must be taken into account in both the design and interpretation of studies to identify biomarkers which will be useful for early detection of cancer. Our recent studies suggest that the combination of antibodies against a group of TAAs might acquire higher sensitivity for diagnosis of cancer. It is conceivable that autoantibody profiles involving different panels or arrays of TAAs might be developed in the future and the results could be useful for cancer diagnosis.
癌症血清中含有与一组独特的自体细胞抗原发生反应的抗体,这些抗原被称为肿瘤相关抗原(TAAs)。长期以来,癌症一直被认为是一个多步骤过程,不仅涉及赋予生长优势的基因变化,还涉及破坏生长和分化调节的因素。有可能识别出其中一些因素,并借助肿瘤发生过程中产生的自身抗体评估它们的功能。在设计和解释旨在识别对癌症早期检测有用的生物标志物的研究时,必须考虑人类癌症分子发病机制中的多因素和多步骤性质。我们最近的研究表明,针对一组肿瘤相关抗原的抗体组合可能对癌症诊断具有更高的敏感性。可以想象,未来可能会开发出涉及不同肿瘤相关抗原组合或阵列的自身抗体谱,其结果可能对癌症诊断有用。