| Literature DB >> 25462559 |
Cindy Hodakoski1, Barry Fine2, Benjamin Hopkins1, Ramon Parsons3.
Abstract
The tumor suppressor PTEN dephosphorylates PIP3 to inhibit PI3K signaling in cells. Altering PTEN intracellular signaling can therefore significantly affect cell behavior. Two novel mechanisms of PTEN regulation including the secretion and entry of the translational variant PTEN-L, and enzymatic inhibition by the interacting protein P-REX2, have been shown to modulate PI3K signaling, cellular proliferation and survival, and glucose metabolism. Here, we review the methods used to identify and validate the existence of both PTEN-L and the P-REX2-PTEN complex, to determine their effects on PTEN phosphatase activity, and to examine their role in cellular physiology.Entities:
Keywords: P-REX2; PTEN; PTEN-L; Secretion
Mesh:
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Year: 2014 PMID: 25462559 PMCID: PMC4861994 DOI: 10.1016/j.ymeth.2014.11.008
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608