P F Kue1, Y Daaka. 1. Department of Surgery, Duke University Medical Center, Durham, North Carolina 27710, USA.
Abstract
PURPOSE: G proteins are involved in the regulation of multiple cellular functions, including metabolism and proliferation. We studied the role of Gi/o protein subunits in the growth and survival of prostate cancer cells. MATERIALS AND METHODS: We investigated the effects of pertussis toxin and the G beta gamma sequestrant peptide G protein coupled receptor kinase 2 carboxy terminus on the growth and mitogenic signaling of prostate cells. RESULTS: Pertussis toxin treatment inhibited the lysophosphatidic acid and serum mediated growth of prostate cancer PC-3 cells by 70% to 80% but showed no effect on insulin-like growth factor 1 (IGF-1) or epidermal growth factor (EGF) mediated growth of these cells. Growth and survival of cells are dependent on activation of intracellular signaling cascades, including those of the mitogen activated protein kinase and Akt pathways. Treatment of the PC-3 cells with lysophosphatidic acid, EGF or serum induced an 8-fold increase in the phosphorylation levels of the mitogen activated protein kinases Erk 1 and 2, and a 3-fold increase in the phosphorylation level of Akt. Erk 1/2 and Akt phosphorylation by lysophosphatidic acid and serum was inhibited by pertussis toxin, suggesting a Gi/o subunit dependent mechanism. EGF and IGF-1 mediated increase in phosphorylation of Erk 1/2 and Akt was independent of pertussis toxin action. Expression of the G beta gamma sequestrant peptide G protein coupled receptor kinase 2 carboxy terminus inhibited the lysophosphatidic acid and serum mediated activation of Erk 1/2 and Akt but showed no effect on the IGF-1 or EGF mediated response. Finally, we showed that activation of the Erk 1/2 pathway in the prostate cancer cells by lysophosphatidic acid and serum is dependent on the EGF receptor and c-Src protein tyrosine kinases. Whereas activation of Akt by these stimuli is not dependent on protein tyrosine kinase activation, it is mediated by PI3K. CONCLUSIONS: These data indicate that lysophosphatidic acid and serum induce proliferation and mitogenic signaling of prostate cancer cells. Importantly, the serum mediated growth of these cells is dependent on Gi beta gamma subunits, suggesting an important regulatory role for G proteins in the growth of prostate cancer cells.
PURPOSE: G proteins are involved in the regulation of multiple cellular functions, including metabolism and proliferation. We studied the role of Gi/o protein subunits in the growth and survival of prostate cancer cells. MATERIALS AND METHODS: We investigated the effects of pertussis toxin and the G beta gamma sequestrant peptide G protein coupled receptor kinase 2 carboxy terminus on the growth and mitogenic signaling of prostate cells. RESULTS: Pertussis toxin treatment inhibited the lysophosphatidic acid and serum mediated growth of prostate cancer PC-3 cells by 70% to 80% but showed no effect on insulin-like growth factor 1 (IGF-1) or epidermal growth factor (EGF) mediated growth of these cells. Growth and survival of cells are dependent on activation of intracellular signaling cascades, including those of the mitogen activated protein kinase and Akt pathways. Treatment of the PC-3 cells with lysophosphatidic acid, EGF or serum induced an 8-fold increase in the phosphorylation levels of the mitogen activated protein kinases Erk 1 and 2, and a 3-fold increase in the phosphorylation level of Akt. Erk 1/2 and Akt phosphorylation by lysophosphatidic acid and serum was inhibited by pertussis toxin, suggesting a Gi/o subunit dependent mechanism. EGF and IGF-1 mediated increase in phosphorylation of Erk 1/2 and Akt was independent of pertussis toxin action. Expression of the G beta gamma sequestrant peptide G protein coupled receptor kinase 2 carboxy terminus inhibited the lysophosphatidic acid and serum mediated activation of Erk 1/2 and Akt but showed no effect on the IGF-1 or EGF mediated response. Finally, we showed that activation of the Erk 1/2 pathway in the prostate cancer cells by lysophosphatidic acid and serum is dependent on the EGF receptor and c-Src protein tyrosine kinases. Whereas activation of Akt by these stimuli is not dependent on protein tyrosine kinase activation, it is mediated by PI3K. CONCLUSIONS: These data indicate that lysophosphatidic acid and serum induce proliferation and mitogenic signaling of prostate cancer cells. Importantly, the serum mediated growth of these cells is dependent on Gi beta gamma subunits, suggesting an important regulatory role for G proteins in the growth of prostate cancer cells.
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