中国中医药信息杂志
中國中醫藥信息雜誌
중국중의약신식잡지
CHINESE JOURNAL OF INFORMATION ON TRADITIONAL CHINESE MEDICINE
2015年
3期
60-64
,共5页
周昱岐%叶敏%吕灿%魏品康
週昱岐%葉敏%呂燦%魏品康
주욱기%협민%려찬%위품강
结直肠癌%消痰散结方%细胞增殖%细胞凋亡%Caspase3蛋白
結直腸癌%消痰散結方%細胞增殖%細胞凋亡%Caspase3蛋白
결직장암%소담산결방%세포증식%세포조망%Caspase3단백
colorectal cancer%Xiaotan Sanjie Recipe%cell proliferation%cell apoptosis%Caspase3
目的:探讨消痰散结方对结直肠癌细胞系增殖、凋亡的影响。方法消痰散结方浸膏冻干粉末溶解在细胞培养液中,制备消痰散结方保存液。以不同浓度消痰散结方作用HCT116细胞72 h,CCK-8法检测细胞增殖;取0.94、1.88 mg/mL消痰散结方作用于HCT116细胞24、48、72 h,CCK-8法检测细胞增殖;消痰散结方(0.24、0.47、0.94、1.88 mg/mL)作用细胞72 h后,TUNEL法原位检测细胞凋亡,计算细胞凋亡率;Western blot检测药物干预后 Caspase3蛋白表达变化。结果消痰散结方对 HCT116细胞增殖有抑制作用,作用72 h IC50为0.94 mg/mL,抑制作用呈浓度-时间依赖性,药物浓度和作用时间有交互作用;消痰散结方促进HCT116细胞凋亡,随药物浓度增高,凋亡率增高,与对照组比较差异有统计学意义(P<0.01);药物作用后Pro-Caspase3蛋白表达量降低,Cleaved Caspase3蛋白表达量增加。结论消痰散结方在体外对HCT116细胞有抑制增殖、促进凋亡的作用,其机制可能与增强Caspase3活性相关。
目的:探討消痰散結方對結直腸癌細胞繫增殖、凋亡的影響。方法消痰散結方浸膏凍榦粉末溶解在細胞培養液中,製備消痰散結方保存液。以不同濃度消痰散結方作用HCT116細胞72 h,CCK-8法檢測細胞增殖;取0.94、1.88 mg/mL消痰散結方作用于HCT116細胞24、48、72 h,CCK-8法檢測細胞增殖;消痰散結方(0.24、0.47、0.94、1.88 mg/mL)作用細胞72 h後,TUNEL法原位檢測細胞凋亡,計算細胞凋亡率;Western blot檢測藥物榦預後 Caspase3蛋白錶達變化。結果消痰散結方對 HCT116細胞增殖有抑製作用,作用72 h IC50為0.94 mg/mL,抑製作用呈濃度-時間依賴性,藥物濃度和作用時間有交互作用;消痰散結方促進HCT116細胞凋亡,隨藥物濃度增高,凋亡率增高,與對照組比較差異有統計學意義(P<0.01);藥物作用後Pro-Caspase3蛋白錶達量降低,Cleaved Caspase3蛋白錶達量增加。結論消痰散結方在體外對HCT116細胞有抑製增殖、促進凋亡的作用,其機製可能與增彊Caspase3活性相關。
목적:탐토소담산결방대결직장암세포계증식、조망적영향。방법소담산결방침고동간분말용해재세포배양액중,제비소담산결방보존액。이불동농도소담산결방작용HCT116세포72 h,CCK-8법검측세포증식;취0.94、1.88 mg/mL소담산결방작용우HCT116세포24、48、72 h,CCK-8법검측세포증식;소담산결방(0.24、0.47、0.94、1.88 mg/mL)작용세포72 h후,TUNEL법원위검측세포조망,계산세포조망솔;Western blot검측약물간예후 Caspase3단백표체변화。결과소담산결방대 HCT116세포증식유억제작용,작용72 h IC50위0.94 mg/mL,억제작용정농도-시간의뢰성,약물농도화작용시간유교호작용;소담산결방촉진HCT116세포조망,수약물농도증고,조망솔증고,여대조조비교차이유통계학의의(P<0.01);약물작용후Pro-Caspase3단백표체량강저,Cleaved Caspase3단백표체량증가。결론소담산결방재체외대HCT116세포유억제증식、촉진조망적작용,기궤제가능여증강Caspase3활성상관。
Objective To investigate the effects of Xiaotan Sanjie Recipe (XTSJR) on the proliferation and apoptosis of colorectal cancer cell;To study its relevant mechanism. Methods The original XTSJR aqueous solution was lyophilized, weighted, and dissolved in cell culture and stored. HCT116 cell line was treated with different concentrations of XTSJR for 72 h, and the cell proliferation was detected by CCK-8 assay. XTSJR treated HCT116 cell line with the concentration of 0.94 mg/mL and 1.88 mg/mL for 24 h, 48 h, 72 h, and the cell proliferation was detected by CCK-8 assay. HCT116 cell line was treated with different concentrations (0.24, 0.47, 0.94, 1.88 mg/mL) of XTSJR for 72 h. The cell apoptosis was detected by TUNEL assay under the fluorescence microscope, and the post-intervention expression of Caspase3 protein was detected by Western blot. Results The inhibitory effects of XTSJR on the proliferation of HCT116 cell line was concentration-time dependent. The IC50 value at 72 h-time point was 0.94 mg/mL. Medicine concentration and the treated time have interactive contribution to the inhibitory effect. XTSJR induced the cell apoptosis. The apoptosis rate increased with the increasing medicine concentration. There was statistically significant difference compared with the control group ( P<0.01). After treatment the expression of Pro-Caspase3 decreased, while the expression Cleaved Caspase3 protein increased. Conclusion XTSJR inhibits the proliferation of HCT116 cell line and induce apoptosis. Its mechanism might be related to the activity of Caspase3 protein.