Dlxin-1, a member of MAGE family, inhibits cell proliferation, invasion and tumorigenicity of glioma stem cells

被引:19
|
作者
Reddy, E. M. [1 ]
Chettiar, S. T. [1 ]
Kaur, N. [1 ]
Ganeshkumar, R. [1 ]
Shepal, V. [1 ]
Shanbhag, N. C. [1 ]
Shiras, A. [1 ]
机构
[1] NCCS, Pune 411007, Maharashtra, India
关键词
NRAGE; p21; p53; CD133; self-renewal; IN-VITRO; GLIOBLASTOMA CELLS; PROTEIN; IDENTIFICATION; EXPRESSION; APOPTOSIS; SUPPRESSES; MODEL; PHOSPHORYLATION; OVEREXPRESSION;
D O I
10.1038/cgt.2010.71
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have previously reported the presence of Dlxin-1, a member of the melanoma antigen gene (MAGE) family, in the brain and showed its function as a cell cycle arrest protein, suggesting that Dlxin-1 may have anti-proliferative functions in rapidly growing tumors. Using the cancer stem cell hypothesis, which attributes the initiation and progression of brain tumors to the cancer-initiating stem cells, we have investigated the role of Dlxin-1 in the glioma stem cells propagated by us as a cell culture system comprising of HNGC-2 cells. Our studies provide evidence about the role of Dlxin-1 as an anti-tumorigenic protein in the highly chemo-resistant glioma stem cells. Next, we show that these anti-proliferative effects are manifested by Dlxin-1 through down regulation of the activities of MMP-2 and MMP-9, and through interaction of Dlxin-1 with its target protein P311 that is involved in glioma cell invasion. In summary, we establish the roles for Dlxin-1, one as an anti-tumorigenic and anti-invasive protein in high-grade gliomas and the other as an inducer of differentiation of glioma stem cells. These two attributes, in conjunction, result in conversion of the drug-resistant brain tumor stem cells to the tumor-attenuated cells that may now be more amenable to effective therapeutic targeting. Cancer Gene Therapy (2011) 18, 206-218; doi: 10.1038/cgt.2010.71; published online 26 November 2010
引用
收藏
页码:206 / 218
页数:13
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