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Publication : p37δ is a new isoform of PI3K p110δ that increases cell proliferation and is overexpressed in tumors.

First Author  Fransson S Year  2012
Journal  Oncogene Volume  31
Issue  27 Pages  3277-86
PubMed ID  22020336 Mgi Jnum  J:196250
Mgi Id  MGI:5487514 Doi  10.1038/onc.2011.492
Citation  Fransson S, et al. (2012) p37delta is a new isoform of PI3K p110delta that increases cell proliferation and is overexpressed in tumors. Oncogene 31(27):3277-86
abstractText  The phosphatidylinositol 3-kinases (PI3Ks) regulate cell growth, proliferation and survival, and are frequently affected in human cancer. PI3K is composed of a catalytic subunit, p110, and a regulatory subunit, p85. The PI3K catalytic subunit p110delta is encoded by PIK3CD and contains p85- and RAS-binding domains, and a kinase domain. Here we present an alternatively spliced PIK3CD transcript encoding a previously unknown protein, p37delta, and demonstrate that this protein is expressed in human ovarian and colorectal tumors. p37delta retains the p85-binding domain and a fraction of the RAS-binding domain, lacks the catalytic domain, and has a unique carboxyl-terminal region. In contrast to p110delta, which stabilizes p85, p37delta promoted p85 sequestering. Despite the truncated RAS-binding domain, p37delta bound to RAS and we found a strong positive correlation between the protein levels of p37delta and RAS. Overexpressing p37delta, but not p110delta, increased the proliferation and invasive properties of HEK-293 cells and mouse embryonic fibroblasts. Cells overexpressing p37delta showed a quicker phosphorylation response of AKT and ERK1/2 following serum stimulation. Ubiquitous expression of human p37delta in the fruit fly increased body size, DNA content and phosphorylated ERK1/2 levels. Thus, p37delta appears to be a new tumor-specific isoform of p110delta with growth-promoting properties.
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