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Brain tumors and mouse models: New insight into the development of gliomas

r. Holland and colleagues discovered that the timing of PDGF expression can determine which characteristics a particular glioma displays. Dr. Holland found that excess PDGF expression in mature astrocytes may generate gliomas by dedifferentiating the astrocytes into glial progenitor-like cells. Further experiments showed that the severity of the gliomas in both strains of mice could be increased by the loss of an important cell cycle arrest gene. Dr. Holland and colleagues conclude that some low grade gliomas are made up of proliferating glial progenitor cells that are somehow blocked in their ability to differentiate. Meanwhile, high grade malignant gliomas are likely to have acquired additional mutations in genes important in regulating the cell cycle.

Identifying pathways that lead to gliomas is a key step towards the design of new therapeutic strategies for the treatment of these tumors. The fact that the low grade gliomas in these mice consisted of undifferentiated glial progenitor-like cells suggests that these types of tumor may respond well to drugs that promote glial cell differentiation. These mice provide an excellent model for testing such drugs and offer hope for a new generation of glioma therapies.


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Contact: Nora Poppito
poppito@cshl.org
Cold Spring Harbor Laboratory
31-Jul-2001


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