中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2011年
7期
1107-1110
,共4页
卢清军%熊宇%严威%林芬%王效民%吴国洋
盧清軍%熊宇%嚴威%林芬%王效民%吳國洋
로청군%웅우%엄위%림분%왕효민%오국양
二甲双胍%癌,肝细胞%脱噬作用
二甲雙胍%癌,肝細胞%脫噬作用
이갑쌍고%암,간세포%탈서작용
Metformin%Carcinoma,hepatocellular%Apoptosis
目的 观察二甲双胍对人肝癌Hep-G2细胞增殖、凋亡及裸鼠皮下瘤生长的影响.方法 噻唑蓝(MTT)比色法分别检测二甲双胍作用于细胞后其细胞活力及生长抑制率;流式细胞术检测二甲双胍作用后细胞周期时相、凋亡率;免疫印迹法(Western blot)检测凋亡相关蛋白的表达;将Hep-G2细胞接种于裸鼠,观察不同浓度二甲双胍对裸鼠皮下瘤生长的影响.结果 20mmol/L二甲双胍作用细胞48h时,细胞生长周期阻滞于G0/G1期,细胞凋亡率为(20.57±3.16)%;Western blot检测显示bcl-2、bcl-xl蛋白表达随着药物浓度的增加而减少,Bid蛋白表达随着药物浓度增加而增加.高剂量二甲双胍组及联合用药组裸鼠皮下瘤体积显著小于对照组,20d时两组抑瘤率分别为40.8%、72.8%.结论 二甲双胍通过线粒体介导的凋亡通路途径来诱导人肝癌细胞发生凋亡,并抑制肝癌细胞裸鼠瘤生长.
目的 觀察二甲雙胍對人肝癌Hep-G2細胞增殖、凋亡及裸鼠皮下瘤生長的影響.方法 噻唑藍(MTT)比色法分彆檢測二甲雙胍作用于細胞後其細胞活力及生長抑製率;流式細胞術檢測二甲雙胍作用後細胞週期時相、凋亡率;免疫印跡法(Western blot)檢測凋亡相關蛋白的錶達;將Hep-G2細胞接種于裸鼠,觀察不同濃度二甲雙胍對裸鼠皮下瘤生長的影響.結果 20mmol/L二甲雙胍作用細胞48h時,細胞生長週期阻滯于G0/G1期,細胞凋亡率為(20.57±3.16)%;Western blot檢測顯示bcl-2、bcl-xl蛋白錶達隨著藥物濃度的增加而減少,Bid蛋白錶達隨著藥物濃度增加而增加.高劑量二甲雙胍組及聯閤用藥組裸鼠皮下瘤體積顯著小于對照組,20d時兩組抑瘤率分彆為40.8%、72.8%.結論 二甲雙胍通過線粒體介導的凋亡通路途徑來誘導人肝癌細胞髮生凋亡,併抑製肝癌細胞裸鼠瘤生長.
목적 관찰이갑쌍고대인간암Hep-G2세포증식、조망급라서피하류생장적영향.방법 새서람(MTT)비색법분별검측이갑쌍고작용우세포후기세포활력급생장억제솔;류식세포술검측이갑쌍고작용후세포주기시상、조망솔;면역인적법(Western blot)검측조망상관단백적표체;장Hep-G2세포접충우라서,관찰불동농도이갑쌍고대라서피하류생장적영향.결과 20mmol/L이갑쌍고작용세포48h시,세포생장주기조체우G0/G1기,세포조망솔위(20.57±3.16)%;Western blot검측현시bcl-2、bcl-xl단백표체수착약물농도적증가이감소,Bid단백표체수착약물농도증가이증가.고제량이갑쌍고조급연합용약조라서피하류체적현저소우대조조,20d시량조억류솔분별위40.8%、72.8%.결론 이갑쌍고통과선립체개도적조망통로도경래유도인간암세포발생조망,병억제간암세포라서류생장.
Objective To investigate the effect of metformin on proliferation, apoptosis of Hep-G2 cells and tumor growth in nude mice. Methods Hep-G2 cells were treated with metformin at different concentrations, and cell viability was measured by using methyl thiazol tetrazolium (MTT) method. Cell cycle and apoptosis rate were assayed by flow cytometry. The expression of apoptosis-related protein were detected by Western blotting.Nude mice were transplanted with Hep-G2 cells, and tumor growth inhibition rate was detected. Results After Hep-G2 cells were treated with 20 mmol/L metformin for 48 h, the growth cycle was arrested in G0/G1 phase, the apoptosis rate was (20.57±3.16)%, the expression of bcl-2 and bcl-xl proteins was down-regulated after metformin treatment, while the Bid protein was significantly increased, tumor size in the high-dose metformin group, cisplatin combined with metformin group were significantly reduced as compared with control group, and the inhibition rates in the high-dose metformin group, cisplatin combined with metformin group was 40.8% and 72.8% respectively. ConclusionMetformin inhibits proliferation of Hep-G2 cells, and induces apoptosis in vitro and significantly inhibits the growth of hepatocellular carcinoma in nude mice.