Genetically Engineered Mice Lacking a Tumor Suppressor Gene in the CNS
- 詳細技術說明
- To overcome the early embryonic lethal phenotype in PTEN(-/-) mice and to study the roles of PTEN in embryonic development, adult tissue function, and tumorigenesis, researchers at UCLA have generated a knockout mouse model with the PTEN gene functionally deleted in neural stem cells. The mouse model can be used in the following applications: 1) preclinical screening for compounds with activities that target the PTEN-controlled signaling pathways in treating cancer and other neurological abnormalities; 2) stemcell research for understanding how PTEN is involved in neural stem cell development, neural regeneration, and neuronal differentiation.
- *Abstract
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None
- *Principal Investigation
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Name: Rebecca Erickson
Department:
Name: Matthias Groszer
Department:
Name: Harley Kornblum
Department:
Name: Xin Liu
Department:
Name: Hong Wu
Department:
- 其他
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Background
Mutation in the PTEN tumor suppressor gene is associated with several human cancers and neurological abnormalities, such as enlarged brain (megacephaly), mental retardation, and malignant brain tumors. Inactivation of PTEN in mouse models confirmed PTEN to be a bona fide tumor suppressor. However, since a null mutation of the gene leads to death during embryogenesis, there hasnt been a defined in vivo model for studying the exact functions of PTEN in brain development and tumor formation.
Related Materials
Negative regulation of neural stem/progenitor cell proliferation by the Pten tumor suppressor gene in vivo. Science. (2001)
Cre/loxP-Mediated Inactivation for the Murine Pten Tumor Suppressor Gene. Genesis. (2002)Additional Technologies by these Inventors
- A Method for In Vivo Visualization of Mutated Mouse Cells
- PTEN Null Cell Lines
- Adipose Tissue-specific PTEN Knockout Mice
- Murine PTEN Null Prostate Cancer Model
Tech ID/UC Case
20321/2003-053-0
Related Cases
2003-053-0
- 國家/地區
- 美國
