CD133 Is Essential for Glioblastoma Stem Cell Maintenance

被引:190
|
作者
Brescia, Paola [1 ]
Ortensi, Barbara [1 ]
Fornasari, Lorenzo [1 ]
Levi, Daniel [2 ]
Broggi, Giovanni [2 ]
Pelicci, Giuliana [1 ]
机构
[1] European Inst Oncol, Dept Expt Oncol, I-20139 Milan, Italy
[2] Fdn IRCCS Ist Neurol C Besta, Dept Neurosurg, Milan, Italy
关键词
Cancer stem cell; CD133; Glioblastoma; Self-renewal; HEMATOPOIETIC STEM; GROWTH-CHARACTERISTICS; IN-VITRO; EXPRESSION; MARKER; IDENTIFICATION; DIFFERENTIATION; PROMOTES; TUMORS; AC133;
D O I
10.1002/stem.1317
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The role of the cell surface CD133 as a cancer stem cell marker in glioblastoma (GBM) has been widely investigated, since it identifies cells that are able to initiate neuro-sphere growth and form heterogeneous tumors when transplanted in immune-compromised mice. However, evidences of CD133-negative cells exhibiting similar properties have also been reported. Moreover, the functional role of CD133 in cancer stem/progenitor cells remains poorly understood. We studied the biological effects of CD133 downregulation in GBM patient-derived neurospheres. Our results indicate that there is not a hierarchical relation between CD133-positive and CD133-negative cells composing the neurospheres. Indeed, CD133 appears in an interconvertible state, changing its subcellular localization between the cytoplasm and the plasmamembrane of neurosphere cells. Silencing of CD133 in human GBM neurospheres using lentivirus-mediated short hairpin RNA impairs the self-renewal and tumorigenic capacity of neurosphere cells. These results imply that CD133 could be used as a therapeutic target in GBMs. STEM CELLS 2013;31:857-869
引用
收藏
页码:857 / 869
页数:13
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