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作 者:胡孙宽[1] 周琴[1] 林铁素[1] 杨云秀[2] 潘钰婷[3] 陈必成[2] 金嵘[4]
机构地区:[1]温州医学院附属第一医院消化内科,浙江温州325000 [2]温州医学院附属第一医院肝胆胰外科,浙江温州325000 [3]九江市第一人民医院ICU,江西九江332000 [4]温州医学院附属第一医院流行病学教研室,浙江温州325000
出 处:《中国药理学与毒理学杂志》2013年第1期72-76,共5页Chinese Journal of Pharmacology and Toxicology
基 金:浙江省自然科学基金(Y2101458);温州市高层次人才创新技术项目重点资助(201011)~~
摘 要:目的观察选择性环氧化酶2(COX-2)抑制剂NS-398对胃癌细胞AGS增殖的抑制作用,并探讨其相关机制。方法 NS-398 25,50和100μmol·L-1作用于AGS细胞0~48 h,用CCK-8法检测细胞存活率。NS-398 50μmol·L-1作用于AGS细胞48 h,用流式细胞仪检测细胞凋亡率,实时荧光定量PCR检测Notch信号通路相关基因的表达,Western印迹法检测Notch胞内结构域(NICD)及下游靶基因NF-κB和毛蛋白和断裂1增强子(Hes-1)蛋白表达。结果 NS-398 25,50和100μmol·L-1能抑制胃癌细胞AGS增殖,并呈时间(r时间=-1.00,P=0.003,50μmol·L-1)和浓度(r浓度=-0.999,P=0.027,48 h)依赖性。NS-39850μmol·L-1作用48 h,AGS细胞凋亡率为(20.1±3.5)%,比正常对照组(3.5±1.4)%明显增加(P<0.05);Notch信号通路受体Notch1和Notch2及Notch信号通路配体δ样1(DLL1)和锯齿状1(JAG1)mRNA表达无明显变化,Notch下游靶基因Hes-1和NF-κB mRNA表达较正常对照组明显减少(P<0.05);NICD,Hes-1和NF-κB蛋白表达明显减少(P<0.05)。结论选择性COX-2抑制剂NS-398可能通过抑制Notch信号途径抑制胃癌细胞AGS增殖。OBJECTIVE To investigate the inhibition of cyclooxygenase-2 selective inhibitor NS-398 on gas- tric cancer cell proliferation and the possible mechanism. METHODS After AGS cells were treated with NS-398 25, 50 and 100 μmol· L^-1 for 48 h, AGS cell viability was determined by CCK-8 assay. Flow cytometric analysis was used to detect the apoptosis of AGS cells after 48 h treatment with NS-398 50 μmol· L^-1. The expression of Notch signal pathway related genes was evaluated by real-time PCR. The protein expression of Notch intracellular domain (NICD), NF-KB2 and Hes-1 (hairy and enhancer of split 1 ) in AGS cells was determined by Western blotting. RESULTS Treatment with NS-398 potently induced apoptosis of AGS cells in a time-(rTirne = -1.00, P =0. 003, 50 μmol· L^-1) and concentration- rconcentration = -0. 999, P=0. 027, 48 h) dependent manner. The apoptosis rate of AGS cells treated with NS-398 50 μmol· L^-1 for 48 h increased to (20.1 ± 3.5) % compared with the control group (3.5 ± 1.4) % ( P 〈0.05). In addition, the rnRNA expression of Hes-1 and NF-KB2 was reduced ( P 〈 0.05) 24 h after treatment of NS-398 50 μmol· L^-1 while Notch1, Notch2, DLL1 (delta like 1 ) and JAG1 (jagged-1) mRNA expression was not changed obviously. Moreover, NICD, Hes-1 and NF-KB2 protein expression was decreased ( P 〈 0. 05 ). CONCLUSION The cyclooxygenase-2 selective inhibitor NS-398 reduces proliferation of AGS gastric cancer cells through the Notch signal pathway.
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