Therapeutic Targeting of Developmental Signaling Pathways in Medulloblastoma: Hedgehog, Notch, Wnt and Myc

被引:0
|
作者
Raabe, Eric [1 ,2 ,3 ,4 ]
Eberhart, Charles G.
机构
[1] Johns Hopkins Univ, Dept Pediat, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Oncol, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Dept Pathol, Baltimore, MD 21218 USA
[4] Johns Hopkins Univ, Dept Ophthalmol, Baltimore, MD 21218 USA
关键词
Non-genotoxic therapy; primitive neuroectodermal tumor; gamma secretase; tankyrase; glutamine; cyclopamine; itraconazole; PRIMITIVE NEUROECTODERMAL TUMORS; LOVASTATIN-INDUCED APOPTOSIS; GRANULE NEURON PRECURSORS; SMALL-MOLECULE INHIBITORS; EMBRYONAL BRAIN-TUMORS; CENTRAL-NERVOUS-SYSTEM; BETA-CATENIN STATUS; CANCER-CELL-GROWTH; C-MYC; MOUSE MODEL;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
During development of the cerebellum, a large number of molecular factors interact to produce an intricate brain structure. Many of these developmentally significant genes are members of signaling cascades implicated in the formation and growth of the embryonal brain tumor medulloblastoma. Genes controlling critical developmental pathways such as Hedgehog, Notch, Wnt, and Myc are known to be overexpressed and/or genetically altered in subsets of medulloblastoma. These pathways are also linked by their ability to induce or maintain stem-cell phenotypes in normal development. Their over-activation in tumors can lead to proliferation, invasion, altered metabolism, and evasion of treatment-induced cell death. The importance of these signaling cascades in medulloblastoma cells makes them attractive targets for therapeutic intervention. The development of therapeutic agents targeting these pathways may lead to improvement in patient survival and a reduction in the intensity of highly morbid radiation and chemotherapy that patients currently receive. In this review, we discuss a number of approaches to targeting these pathways in medulloblastoma.
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收藏
页码:55 / 66
页数:12
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