Medulloblastoma, the most common pediatric malignant tumor, arises from the granule cell precursors (GCPs) in the cerebellum. Sonic hedgehog (Shh)/Patched signaling tightly regulates the proliferation of the GCPs during development. Deregulation of this pathway results in uncontrolled growth and subsequent medulloblastoma formation in both humans and mice. Using a mouse model of medulloblastoma with reduced Patchedl function, we have identified molecular events contributing to early and late tumor lesions in the cerebellum through expression analyses. This proposal is focused on determining the roles of these factors in the developing cerebellum, the mechanisms by which they regulate cell division of the GCPs, and how they cooperate with the Shh/Patched signaling pathway to promote cellular proliferation during normal development and tumorigenesis of the cerebellum. A deeper understanding of the complex signaling networks underlying the proliferation and oncogenic transformation of the cerebellar precursor cells will reveal new targets for developing effective treatments. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32CA117775-03
Application #
7289823
Study Section
Special Emphasis Panel (ZRG1-F09 (20))
Program Officer
Jakowlew, Sonia B
Project Start
2005-09-01
Project End
2008-04-28
Budget Start
2007-09-01
Budget End
2008-04-28
Support Year
3
Fiscal Year
2007
Total Cost
$32,256
Indirect Cost
Name
Stanford University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
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Lee, Eunice Y; Ji, Hongkai; Ouyang, Zhengqing et al. (2010) Hedgehog pathway-regulated gene networks in cerebellum development and tumorigenesis. Proc Natl Acad Sci U S A 107:9736-41
Corcoran, Ryan B; Bachar Raveh, Tal; Barakat, Monique T et al. (2008) Insulin-like growth factor 2 is required for progression to advanced medulloblastoma in patched1 heterozygous mice. Cancer Res 68:8788-95