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Effect of nimesulide on proliferation,apoptosis and protein expression related to STAT3 signaling pathway in SGC-7901 cells

Chen Min

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Abstract

Objective:To investigate the inhibition effect of proliferation of gastric cancer cell line SGC7901 treated with selective cyclooxgenase 2(COX-2)inhibitor,nimesulide,and the probable mechanism of cell signal transduction.Methods: SGC7901 cells were treated with nimesulide.MTT assay was used to measure the cell proliferation;Flow cytometry was used to detect cell cycle and apoptosis.The protein expression related to STAT3 signaling pathway in SGC7901 cells was examined by Western blot.Results:The growth of gastric cancer cells was obviously inhibited in a time-and dose-dependent manner after nimesulide treatment;the percentage of apoptosis was increased significantly(P0.05);the proportion of SGC7901 in G_0/G_1 phase was hoisted significantly(P0.05);Western blot analysis showed that:the protein expression of phosphorylated STAT3(P-STAT3), CyclinD1,Bcl-2 in SGC-7901 cells was decreased significantly(P0.05).Conclusions:The proliferation of gastric cancer cell line SGC7901 could be inhibited;the course of cell cycle could be prevented;cell apoptosis could be induced by nimesulide through down-regulating the protein expression of P-STAT3,CyclinD1,Bcl-2,which was probably one of its molecular mechanisms.

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Objective:To investigate the inhibition effect of proliferation of gastric cancer cell line SGC7901 treated with selective cyclooxgenase 2(COX-2)inhibitor,nimesulide,and the probable mechanism of cell signal transduction.Methods: SGC7901 cells were treated with nimesulide.MTT assay was used to measure the cell proliferation;Flow cytometry was used to detect cell cycle and apoptosis.The protein expression related to STAT3 signaling pathway in SGC7901 cells was examined by Western blot.Results:The growth of gastric cancer cells was obviously inhibited in a time-and dose-dependent manner after nimesulide treatment;the percentage of apoptosis was increased significantly(P0.05);the proportion of SGC7901 in G_0/G_1 phase was hoisted significantly(P0.05);Western blot analysis showed that:the protein expression of phosphorylated STAT3(P-STAT3), CyclinD1,Bcl-2 in SGC-7901 cells was decreased significantly(P0.05).Conclusions:The proliferation of gastric cancer cell line SGC7901 could be inhibited;the course of cell cycle could be prevented;cell apoptosis could be induced by nimesulide through down-regulating the protein expression of P-STAT3,CyclinD1,Bcl-2,which was probably one of its molecular mechanisms.

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Available abstract

Objective:To investigate the inhibition effect of proliferation of gastric cancer cell line SGC7901 treated with selective cyclooxgenase 2(COX-2)inhibitor,nimesulide,and the probable mechanism of cell signal transduction.Methods: SGC7901 cells were treated with nimesulide.MTT assay was used to measure the cell proliferation;Flow cytometry was used to detect cell cycle and apoptosis.The protein expression related to STAT3 signaling pathway in SGC7901 cells was examined by Western blot.Results:The growth of gastric cancer cells was obviously inhibited in a time-and dose-dependent manner after nimesulide treatment;the percentage of apoptosis was increased significantly(P0.05);the proportion of SGC7901 in G_0/G_1 phase was hoisted significantly(P0.05);Western blot analysis showed that:the protein expression of phosphorylated STAT3(P-STAT3), CyclinD1,Bcl-2 in SGC-7901 cells was decreased significantly(P0.05).Conclusions:The proliferation of gastric cancer cell line SGC7901 could be inhibited;the course of cell cycle could be prevented;cell apoptosis could be induced by nimesulide through down-regulating the protein expression of P-STAT3,CyclinD1,Bcl-2,which was probably one of its molecular mechanisms.

Key concepts: Nimesulide, Apoptosis, Cell cycle, Western blot, Cell growth, Flow cytometry, Signal transduction, Molecular biology

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Effect of nimesulide on proliferation,apoptosis and protein expression related to STAT3 signaling pathway in SGC-7901 cells — Research Paper | ScholarLens