Abstract
Aim: To investigate whether Src, JAK2 and phosphatidylinositol 3-kinase (PI3K) pathways are involved in the proliferation of human colonic tumour cells induced by glycine-extended gastrin (G-gly), the precursor of the mature amidated gastrin and to elucidate the molecular interaction between these three kinases in response to this peptide. Methods: Using the human colonic tumour cell line HCT116 as a model, we first measured the activation of PI3K, p60-Src and JAK2 in response to G-gly by in vitro kinase assays. Then we investigated the involvement of these kinases in G-gly-induced cell proliferation by MTT test. Results: G-gly stimulation induced p60-Src, JAK2 and PI3K activation in HCT-116. The different pathways were involved in proliferation of human colon cancer cells induced by G-gly. Furthermore, we found that both Src and JAK2 were necessary to PI3K regulation by this peptide. However, we did not find any cross-talk between the two tyrosine kinases. Conclusion: Our results suggest that the p60-Srq/PI3K and JAK2/PI3K pathways act independently to mediate G-gly proliferative effect on human colonic tumour cells. © 2006 The WJG Press. All rights reserved.
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Ferrand, A., Kowalski-Chauvel, A., Pannequin, J., Bertrand, C., Fourmy, D., Dufresne, M., & Seva, C. (2006). Glycine-extended gastrin activates two independent tyrosine-kinases in upstream of p85/p110 phosphatidylinositol 3-kinase in human colonic tumour cells. World Journal of Gastroenterology, 12(12), 1859–1864. https://doi.org/10.3748/wjg.v12.i12.1859
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