中华消化杂志
中華消化雜誌
중화소화잡지
Chinese Journal of Digestion
2010年
1期
33-36
,共4页
张燕捷%王碧君%程芃%包玉洁%朱黎明%杨文燕%戴强%江佛湖
張燕捷%王碧君%程芃%包玉潔%硃黎明%楊文燕%戴彊%江彿湖
장연첩%왕벽군%정봉%포옥길%주려명%양문연%대강%강불호
胃肿瘤%尼美舒利%细胞凋亡%癌性锚蛋白重复序列
胃腫瘤%尼美舒利%細胞凋亡%癌性錨蛋白重複序列
위종류%니미서리%세포조망%암성묘단백중복서렬
Stomach neoplasms%Nimesulide%Apoptosis%Gankyrin
目的 探讨癌性锚蛋白重复序列(Gankyrin)在人胃癌细胞的表达,以及在尼美舒利诱导细胞凋亡过程中的改变.方法 培养不同分化程度的人胃癌细胞系[MKN28(高分化)、AGS(低分化)、MKN45(低分化)和SGC7901(中分化)],以尼美舒利处理细胞,应用四甲基偶氮唑盐试验和流式细胞术检测细胞活力及细胞凋亡,实时PCR和Western印迹法检测Gankyrin基因和蛋白表达.结果 在4种不同分化程度的人胃癌细胞系中,均存在不同水平的Gankyrin基因和蛋白表达.尼美舒利以时间-剂量依赖方式抑制AGS、FYGC7901细胞增殖.与对照组相比,尼美舒利400 μmol/L处理48 h可诱导AGS、SGC7901细胞显著凋亡(细胞凋亡率分别为0.57%±0.19%比23.30%±2.50%和0.88%±0.17%比16.80%±1.55%,P均<0.01).在AGS细胞凋亡过程中,Gankyrin基因和蛋白表达水平下降,以尼美舒利作用后24 h(0.0035±0.0014)和36 h(0.0980±0.0160)改变最为显著(对照组为0.4690±0.1190,P值均<0.01).结论 在人胃癌细胞中存在Gankyrin基因和蛋白表达.Gankyrin可能参与尼美舒利诱导的AGS胃癌细胞凋亡.
目的 探討癌性錨蛋白重複序列(Gankyrin)在人胃癌細胞的錶達,以及在尼美舒利誘導細胞凋亡過程中的改變.方法 培養不同分化程度的人胃癌細胞繫[MKN28(高分化)、AGS(低分化)、MKN45(低分化)和SGC7901(中分化)],以尼美舒利處理細胞,應用四甲基偶氮唑鹽試驗和流式細胞術檢測細胞活力及細胞凋亡,實時PCR和Western印跡法檢測Gankyrin基因和蛋白錶達.結果 在4種不同分化程度的人胃癌細胞繫中,均存在不同水平的Gankyrin基因和蛋白錶達.尼美舒利以時間-劑量依賴方式抑製AGS、FYGC7901細胞增殖.與對照組相比,尼美舒利400 μmol/L處理48 h可誘導AGS、SGC7901細胞顯著凋亡(細胞凋亡率分彆為0.57%±0.19%比23.30%±2.50%和0.88%±0.17%比16.80%±1.55%,P均<0.01).在AGS細胞凋亡過程中,Gankyrin基因和蛋白錶達水平下降,以尼美舒利作用後24 h(0.0035±0.0014)和36 h(0.0980±0.0160)改變最為顯著(對照組為0.4690±0.1190,P值均<0.01).結論 在人胃癌細胞中存在Gankyrin基因和蛋白錶達.Gankyrin可能參與尼美舒利誘導的AGS胃癌細胞凋亡.
목적 탐토암성묘단백중복서렬(Gankyrin)재인위암세포적표체,이급재니미서리유도세포조망과정중적개변.방법 배양불동분화정도적인위암세포계[MKN28(고분화)、AGS(저분화)、MKN45(저분화)화SGC7901(중분화)],이니미서리처리세포,응용사갑기우담서염시험화류식세포술검측세포활력급세포조망,실시PCR화Western인적법검측Gankyrin기인화단백표체.결과 재4충불동분화정도적인위암세포계중,균존재불동수평적Gankyrin기인화단백표체.니미서리이시간-제량의뢰방식억제AGS、FYGC7901세포증식.여대조조상비,니미서리400 μmol/L처리48 h가유도AGS、SGC7901세포현저조망(세포조망솔분별위0.57%±0.19%비23.30%±2.50%화0.88%±0.17%비16.80%±1.55%,P균<0.01).재AGS세포조망과정중,Gankyrin기인화단백표체수평하강,이니미서리작용후24 h(0.0035±0.0014)화36 h(0.0980±0.0160)개변최위현저(대조조위0.4690±0.1190,P치균<0.01).결론 재인위암세포중존재Gankyrin기인화단백표체.Gankyrin가능삼여니미서리유도적AGS위암세포조망.
Objective To elucidate the expression of gankyrin in human gastric cancer cells and it's role in nimesulide induced apoptosis. Methods Four human gastric cancer cell lines including MKN28 (well differentiated), AGS (poorly differentiated), MKN45 (poorly differentiated), and SGC7901(moderately differentiated) were cultured and treated with nimesulide. Nimesulide induced growth inhibition and apoptosis of the cells were detected by methyl thiazolyl tetrazolium assay, and confirmed by flow cytometry. The expressions of gankyrin gene and protein were further assessed by real-time PCR and Western blotting. Results Gankyrin mRNA and protein were detected in all four human gastric cancer cell lines. The proliferations of AGS and SGC7901 cell lines were significantly suppressed by nimesulide in a time-dose dependent manner. When treated with 400 μmol/L of nimesulide for 48 hours, the significant apoptosis was found in AGS cells (23.30%±2.50%) and SGC7901 cells (16.80%±1.55% ) in comparison with controls (0.57%±0.19% and 0.88%± 0.17%, respectively, all P values <0.01). Apoptosis of AGS cells induced by nimesulide was accompanied by a considerably decreased gankyrin expression that was more significant at 24 hours (0.0035±0.0014) and 36 hours (0.0980±0.0160) in comparison with controls (0.4690±0.1190, all P values<0.01). Conclusion Gankyrin expresses in human gastric cancer cell lines and may be involved in nimesulide induced apoptosis of AGS cells.