Mesenchymal differentiation of glioblastoma stem cells

被引:86
|
作者
Ricci-Vitiani, L. [1 ]
Pallini, R. [2 ]
Larocca, L. M. [3 ]
Lombardi, D. G. [4 ]
Signore, M. [1 ]
Pierconti, F. [3 ]
Petrucci, G. [3 ]
Montano, N. [2 ]
Maira, G. [2 ]
De Maria, R. [1 ,4 ]
机构
[1] Ist Super Sanita, Dept Hematol Oncol & Mol Med, I-00161 Rome, Italy
[2] Univ Cattolica Sacro Cuore, Inst Neurosurg, Rome, Italy
[3] Univ Cattolica Sacro Cuore, Inst Pathol Anat, Rome, Italy
[4] Mediterranean Inst Oncol, Catania, Italy
来源
CELL DEATH AND DIFFERENTIATION | 2008年 / 15卷 / 09期
关键词
cancer stem cells; glioblastoma; mesenchymal potential; differentiation;
D O I
10.1038/cdd.2008.72
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glioblastoma multiforme is a severe form of cancer most likely arising from the transformation of stem or progenitor cells resident in the brain. Although the tumorigenic population in glioblastoma is defined as composed by cancer stem cells (CSCs), the cellular target of the transformation hit remains to be identified. Glioma stem cells (SCs) are thought to have a differentiation potential restricted to the neural lineage. However, using orthotopic versus heterotopic xenograft models and in vitro differentiation assays, we found that a subset of glioblastomas contained CSCs with both neural and mesenchymal potential. Subcutaneous injection of CSCs or single CSC clones from two of seven patients produced tumor xenografts containing osteochondrogenic areas in the context of glioblastoma-like tumor lesions. Moreover, CSC clones from four of seven cases generated both neural and chondrogenic cells in vitro. Interestingly, mesenchymal differentiation of the tumor xenografts was associated with reduction of both growth rate and mitotic index. These findings suggest that in a subclass of glioblastomas the tumorigenic hit occurs on a multipotent stem cell, which may reveal its plasticity under specific environmental stimuli. The discovery of such biological properties might provide considerable information to the development of new therapeutic strategies aimed at forcing glioblastoma stem cell differentiation.
引用
收藏
页码:1491 / 1498
页数:8
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