Phosphatase and tensin homolog deleted on chromosome 10 () is one of the most frequently mutated, deleted, and functionally inactivated tumor suppressor genes in human cancer. is found mutated both somatically and in the germline of patients with PTEN hamartoma tumor syndrome (PHTS). encodes a dual lipid and protein phosphatase that dephosphorylates the lipid phosphatidylinositol-3,4,5-trisphosphate (PIP), in turn negatively regulating the oncogenic PI3K-AKT pathway, a key proto-oncogenic player in cancer development and progression. Because of importance of PTEN in tumorigenesis, a large number of sophisticated genetically engineered mouse models (GEMMs) has been designed to elucidate the underlying mechanisms by which the "PTEN pathway" promotes tumorigenesis, while simultaneously providing a well-tailored system for the identification of novel therapies and offering platforms for new drug discoveries. This review summarizes the major cancer mouse models through which the PTEN pathway has been genetically deconstructed, and outlines the rapid development of GEMMs toward more detailed functional and tissue-specific analysis.
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| http://dx.doi.org/10.1101/cshperspect.a037283 | DOI Listing |
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