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Abstract
The prevailing dogma is that heterotrimeric G proteins exclusively transduce signals from the seven-transmembrane motif–containing cell surface receptors, also known as G protein–coupled receptors (GPCRs). New evidence indicates that Gα13, the α subunit of the G protein G13, breaks away from this traditional exclusive signaling alliance with GPCRs to transmit signals from receptor tyrosine kinases (RTKs), such as platelet-derived growth factor receptor (PDGFR), epidermal growth factor receptor (EGFR), and vascular endothelial growth factor receptor (VEGFR). Gα13 is involved in cell migration in response to GPCRs activated by lysophosphatidic acid (LPA) or thrombin. A new report indicates that Gα13 is also required for cell migration induced by the growth factors, such as PDGF, EGF, or VEGF. GPCR coupling is not required for such RTK-to-Gα13 signaling. This new identity for Gα13 as a signal transducer for both GPCRs and RTKs may be a forerunner for similar findings involving other Gα subunits. This expanding role of G proteins in both GPCR signaling and RTK signaling is likely to have a great impact not only on our understanding of cell signaling in general, but also more specifically where the dysregulation of signaling by GPCRs, RTKs, and G proteins cause pathophysiological changes such as in the case of tumorigenesis, tumor progression and/or metastasis.
