Tumor Pathophysiology, OncoRay, National Center for Radiation Research in Oncology, Dresden University of Technology, Fetscherstrasse 74, Dresden, Germany.
J Pathol. 2013 Feb;229(3):355-78. doi: 10.1002/path.4086. Epub 2012 Nov 20.
The cancer stem cell (CSC) hypothesis, despite the limitations of the currently available models and assays, has ushered in a new era of excitement in cancer research. The development of novel strategies for anti-tumour therapy relies on the use of biomarkers to identify, enrich, and/or isolate the cell population(s) of interest. In this context, various cell characteristics and antigen expression profiles are discussed as surrogate markers. The cell surface expression of the human prominin-1 (CD133) antigen, in particular of the AC133 epitope, is among those that have been most frequently studied in solid cancers, although no mechanism has yet been proposed to link CD133 expression with the CSC phenotype. Some inconsistencies between published data can be ascribed to different analytical tools as well as methodological limitations and pitfalls, highlighted in the present review. Therefore, a comprehensive overview on the current state of knowledge in this growing and exciting field with an emphasis on the most recent studies is presented. We highlight the link between the tumour microenvironment, tumour cell plasticity, and CD133 expression, and evaluate the utility of CD133 expression as a prognostic marker.
癌症干细胞 (CSC) 假说,尽管目前可用的模型和检测方法存在局限性,但它为癌症研究带来了一个新的令人兴奋的时代。新型抗肿瘤治疗策略的开发依赖于使用生物标志物来识别、富集和/或分离感兴趣的细胞群体。在这种情况下,各种细胞特征和抗原表达谱被讨论为替代标志物。人 Prominin-1(CD133)抗原的细胞表面表达,特别是 AC133 表位的表达,是实体瘤中研究最多的标志物之一,尽管尚未提出将 CD133 表达与 CSC 表型联系起来的机制。发表的数据之间的一些不一致可以归因于不同的分析工具以及方法学限制和陷阱,本综述强调了这一点。因此,本文对这个不断发展和令人兴奋的领域的最新研究进展进行了全面概述。我们强调了肿瘤微环境、肿瘤细胞可塑性和 CD133 表达之间的联系,并评估了 CD133 表达作为预后标志物的效用。