The p75 neurotrophin receptor is a central regulator of glioma invasion

被引:140
|
作者
Johnston, Angela L. M.
Lun, Xueqing
Rahn, Jennifer J.
Liacini, Abdelhamid
Wang, Limei
Hamilton, Mark G.
Parney, Ian F.
Hempstead, Barbara L.
Robbins, Stephen M.
Forsyth, Peter A. [1 ]
Senger, Donna L.
机构
[1] Univ Calgary, Dept Biochem & Mol Biol, Calgary, AB, Canada
[2] So Alberta Canc Res Inst, Calgary, AB, Canada
[3] Clark H Smith Integrat Brain Tumour Res Ctr, Calgary, AB, Canada
[4] Univ Calgary, Dept Oncol, Calgary, AB, Canada
[5] Univ Calgary, Dept Clin Neurosci, Calgary, AB, Canada
[6] Cornell Univ, Coll Med, Div Hematol, New York, NY 10021 USA
来源
PLOS BIOLOGY | 2007年 / 5卷 / 08期
关键词
D O I
10.1371/journal.pbio.0050212
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
The invasive nature of cancers in general, and malignant gliomas in particular, is a major clinical problem rendering tumors incurable by conventional therapies. Using a novel invasive glioma mouse model established by serial in vivo selection, we identified the p75 neurotrophin receptor (p75(NTR)) as a critical regulator of glioma invasion. Through a series of functional, biochemical, and clinical studies, we found that p75(NTR) dramatically enhanced migration and invasion of genetically distinct glioma and frequently exhibited robust expression in highly invasive glioblastoma patient specimens. Moreover, we found that p75(NTR)-mediated invasion was neurotrophin dependent, resulting in the activation of downstream pathways and producing striking cytoskeletal changes of the invading cells. These results provide the first evidence for p75(NTR) as a major contributor to the highly invasive nature of malignant gliomas and identify a novel therapeutic target.
引用
收藏
页码:1723 / 1737
页数:15
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