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Mu Yuanyuan, Wu Huichao, Yang Yingying, Su Wei. Effects of Gastrin and Its Antagonist on Cell Proliferation and Expression of HB-EGF in Human Gastric Cancer Line MKN45[J]. Cancer Research on Prevention and Treatment, 2012, 39(02): 133-136. DOI: 10.3971/j.issn.1000-8578.2012.02.004
Citation: Mu Yuanyuan, Wu Huichao, Yang Yingying, Su Wei. Effects of Gastrin and Its Antagonist on Cell Proliferation and Expression of HB-EGF in Human Gastric Cancer Line MKN45[J]. Cancer Research on Prevention and Treatment, 2012, 39(02): 133-136. DOI: 10.3971/j.issn.1000-8578.2012.02.004

Effects of Gastrin and Its Antagonist on Cell Proliferation and Expression of HB-EGF in Human Gastric Cancer Line MKN45

  • Objective To explore the effects of gastrin-17 and its antagonist PGL on cell proliferation and the expression of HB-EGF in human gastric cancer line MKN-45. Methods MKN45 cells were incubated in the medium with gastrin-17 (10-6~10-10 mol/L),proglumide(10-2~10-4 mol/L) or combination of two agents (10-8 mol/L gastrin-17 and 10-2~10-4 mol/L proglumide).Cell growth and proliferation of MKN45 were analyzed by MTT assay,and expression of HB-EGF by Western blot. Results MTT showed gastrin-17 significantly promoted cell proliferation at the concentration of 10-6~10-9 mol/L (P<0.05),PGL at the concentration of 10-2~10-3 mol/L significantly inhibited the proliferation of MKN45 cells (P<0.05).In the combination of two agents,PGL (10-2~10-3 mol/L) significantly inhibite the proliferation of MKN-45 cells induced by gastrin-17 (P<0.05).Meanwhile,MKN45 had the expression of HB-EGF protein which significantly up-regulated by Gastrin-17 at the concertration of 10-6~10-9 mol/L.In the combination of two agents,PGL (10-2~10-3 mol/L) significantly inhibited the expression of HB-EGF stimulated by gastrin-17(P<0.05). Conclusion Gastrin-17 could promote cell proliferation of MKN45 cells in human gastric cancer,which strongly down-regulated by its antagonist PGL.Gastrin-17 significantly promoted the expression of HB-EGF,contrastly and inhibited an antagonist PGL.
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