中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2014年
4期
763-764,后插1
,共3页
郑幼伟%刘海潮%买二辉%孟冬冬%苏宝威%董瑞强
鄭幼偉%劉海潮%買二輝%孟鼕鼕%囌寶威%董瑞彊
정유위%류해조%매이휘%맹동동%소보위%동서강
癌,肝细胞%肿瘤抑素%T42肽%半胱氨酰天冬氨酸特异性蛋白酶-3
癌,肝細胞%腫瘤抑素%T42肽%半胱氨酰天鼕氨痠特異性蛋白酶-3
암,간세포%종류억소%T42태%반광안선천동안산특이성단백매-3
Carcinoma,hepatocellular%Tumstatin%T42 peptide%Cysteinyl aspartate-specific protease-3
目的 探讨肿瘤抑素T42肽在人肝癌裸鼠种植瘤模型诱导凋亡中的作用及机制.方法 建立人肝癌细胞株HCCLM9裸鼠模型,治疗组和对照组(n=10)分别皮下注射T42肽和生理盐水;治疗2周后收集标本,采用原位缺口末端标记法(TUNEL)检测细胞凋亡水平,免疫组织化学方法检测半胱氨酰天冬氨酸特异性蛋白酶(Caspase)-3蛋白的表达.结果 T42肽治疗组肝癌细胞凋亡指数为(8.48±0.58)%,对照组为(2.56±0.48)%,T42肽治疗组显著高于对照组(P<0.05);Caspase-3蛋白在实验组中的阳性表达率为80%,在对照组的阳性表达率为30%,T42肽组显著高于对照组(P<0.05);治疗后T42肽治疗组的瘤体重量为(1.83±0.22)g,对照组为(2.11 ±1.67)g,T42肽治疗组显著低于对照组(P<0.05).结论 T42肽在人肝癌裸鼠模型中可诱导肝癌细胞凋亡,Caspase-3的表达可能在T42肽诱导细胞凋亡的过程中有重要作用.
目的 探討腫瘤抑素T42肽在人肝癌裸鼠種植瘤模型誘導凋亡中的作用及機製.方法 建立人肝癌細胞株HCCLM9裸鼠模型,治療組和對照組(n=10)分彆皮下註射T42肽和生理鹽水;治療2週後收集標本,採用原位缺口末耑標記法(TUNEL)檢測細胞凋亡水平,免疫組織化學方法檢測半胱氨酰天鼕氨痠特異性蛋白酶(Caspase)-3蛋白的錶達.結果 T42肽治療組肝癌細胞凋亡指數為(8.48±0.58)%,對照組為(2.56±0.48)%,T42肽治療組顯著高于對照組(P<0.05);Caspase-3蛋白在實驗組中的暘性錶達率為80%,在對照組的暘性錶達率為30%,T42肽組顯著高于對照組(P<0.05);治療後T42肽治療組的瘤體重量為(1.83±0.22)g,對照組為(2.11 ±1.67)g,T42肽治療組顯著低于對照組(P<0.05).結論 T42肽在人肝癌裸鼠模型中可誘導肝癌細胞凋亡,Caspase-3的錶達可能在T42肽誘導細胞凋亡的過程中有重要作用.
목적 탐토종류억소T42태재인간암라서충식류모형유도조망중적작용급궤제.방법 건립인간암세포주HCCLM9라서모형,치료조화대조조(n=10)분별피하주사T42태화생리염수;치료2주후수집표본,채용원위결구말단표기법(TUNEL)검측세포조망수평,면역조직화학방법검측반광안선천동안산특이성단백매(Caspase)-3단백적표체.결과 T42태치료조간암세포조망지수위(8.48±0.58)%,대조조위(2.56±0.48)%,T42태치료조현저고우대조조(P<0.05);Caspase-3단백재실험조중적양성표체솔위80%,재대조조적양성표체솔위30%,T42태조현저고우대조조(P<0.05);치료후T42태치료조적류체중량위(1.83±0.22)g,대조조위(2.11 ±1.67)g,T42태치료조현저저우대조조(P<0.05).결론 T42태재인간암라서모형중가유도간암세포조망,Caspase-3적표체가능재T42태유도세포조망적과정중유중요작용.
Objective To study the effect of tumstatin T42 peptide on the induced apoptosis of human hepatocellular carcinoma xenografts in nude mice and the possible mechanism.Methods The human hepatoma cell line HCCLM9 nude model was established.The treatment group and control group (n =10 each) were injected subcutaneously with T42 peptide and saline respectively.The specimens after treatment for two weeks were collected.TdT-mediated dUTP nick end labeling (TUNEL) method was used to detect apoptosis levels,and immunohistochemistry to detect Caspase-3 protein expression.Results The apoptosis index in the T42 peptide treatment group was (8.48 ± 0.58) %,and that in the control group was (2.56 ± 0.48) % (P < 0.05).The expression of Caspase-3 in the T42 treatment group was significantly higher than that in the control group (80% vs.30%,P < 0.05).After treatment,the tumor weight in the T42 treatment group was (1.83 ±0.22) g and that in the control group was (2.11 ± 1.67) g (P < 0.05).Conclusion T42 peptide can induce apoptosis of hepatoma cells in human hepatocellular carcinoma of nude mice,which may be contributed to the expression of Caspase-3.