Limits of CD133 as a marker of glioma self-renewing cells

被引:86
作者
Clement, Virginie [1 ]
Dutoit, Valerie [2 ]
Marino, Denis [1 ]
Dietrich, Pierre-Yves [2 ]
Radovanovic, Ivan [1 ]
机构
[1] Univ Hosp Geneva, Ctr Romand Neurochirurg, Dept Neurosurg, CH-1211 Geneva, Switzerland
[2] Univ Hosp Geneva, Dept Oncol, CH-1211 Geneva, Switzerland
关键词
AC133; antigen; brain tumor; glioma self-renewing cells; stem cell marker; CANCER STEM-CELLS; HEMATOPOIETIC STEM; IDENTIFICATION; GROWTH; TUMORS; AC133;
D O I
10.1002/ijc.24352
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In human gliomas, self-renewing and tumor-initiating cells are characterized by the expression marker CD133. Although, widely used, the validity of CD133 is debated as recent data show that CD133(+) and Cb133(-) cells share similar stemness and tumorigenic properties. To clarify this "CD133 controversy", we reexamined the methods of purification and the stem behavior of both CD133 compartments in fresh gliomas and gliomasphere cultures. Using human anti-CD133-coupled microbeads and magnetic activated cell sorting, we observed a nonspecific sorting of glioma cells irrespective of their CD133 expression. In contrast, when purified by fluorescence activating cell sorting, a specific expression and enrichment of CD133 was successfully observed in fresh human gliomas and gliomasphere cultures. However, neither the expression of stemness genes nor the long-term self-renewal capacities of CD133(+) and CD133(-) cells were significantly different, even after fresh isolation. Altogether, our data show that purification of CD133(+) glioma cells using hCD133-microbeads presents a lack of specificity and demonstrate that the use of CD133 as a unique glioma stem cell marker is likely not sufficient to tag the whole self-renewing tumor cell reservoir. (C) 2009 UICC
引用
收藏
页码:244 / 248
页数:5
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