浙江临床医学
浙江臨床醫學
절강림상의학
ZHEJIANG CLINICAL MEDICAL JOURNAL
2014年
7期
1027-1029
,共3页
国宏莉%陈光治%李江华%徐臣利
國宏莉%陳光治%李江華%徐臣利
국굉리%진광치%리강화%서신리
藤梨根/猕猴桃根%食管肿瘤%凋亡%Caspase激活
籐梨根/獼猴桃根%食管腫瘤%凋亡%Caspase激活
등리근/미후도근%식관종류%조망%Caspase격활
Tengligen/Actinidia arguta%Carcinoma of esophagus%Apoptosis%Caspase activation
目的:探讨藤梨根(Actinidia arguta)乙酸乙酯制剂促进人食管癌Eca-109细胞凋亡的机制。方法采用MTT比色法,检测藤梨根乙酸乙酯药液在不同浓度(1μg/ml、10μg/ml、100μg/ml等)及不同时间(24h、48h、72h等)对Eca-109细胞生长抑制作用;采用TUNEL法检测其对癌细胞生长的诱导凋亡效应;采用免疫组化SP法,检测凋亡相关蛋白Bax 、Bcl-2及caspase的表达。结果藤梨根乙酸乙酯药液对人食管癌Eca-109细胞的生长抑制作用,随着药物浓度的升高和作用时间的延长而增强,其生长抑制率可达87.2%。藤梨根制剂对瘤细胞有明显的凋亡效应,而在对照组,未见有明显凋亡现象。瘤细胞作用24h、48h、72h后分别与对照组比较,用药组Bax蛋白表达明显增强(P<0.01);同时伴有Bcl-2表达减弱,72h后最明显,差异有统计学意义(P<0.01)。藤梨根药液促进caspase-3、caspase-9表达明显增强,而对caspase-8表达影响较小。结论藤梨根可通过下调Bcl-2表达,激活caspase-9、caspase-3诱导Eca-109细胞凋亡。
目的:探討籐梨根(Actinidia arguta)乙痠乙酯製劑促進人食管癌Eca-109細胞凋亡的機製。方法採用MTT比色法,檢測籐梨根乙痠乙酯藥液在不同濃度(1μg/ml、10μg/ml、100μg/ml等)及不同時間(24h、48h、72h等)對Eca-109細胞生長抑製作用;採用TUNEL法檢測其對癌細胞生長的誘導凋亡效應;採用免疫組化SP法,檢測凋亡相關蛋白Bax 、Bcl-2及caspase的錶達。結果籐梨根乙痠乙酯藥液對人食管癌Eca-109細胞的生長抑製作用,隨著藥物濃度的升高和作用時間的延長而增彊,其生長抑製率可達87.2%。籐梨根製劑對瘤細胞有明顯的凋亡效應,而在對照組,未見有明顯凋亡現象。瘤細胞作用24h、48h、72h後分彆與對照組比較,用藥組Bax蛋白錶達明顯增彊(P<0.01);同時伴有Bcl-2錶達減弱,72h後最明顯,差異有統計學意義(P<0.01)。籐梨根藥液促進caspase-3、caspase-9錶達明顯增彊,而對caspase-8錶達影響較小。結論籐梨根可通過下調Bcl-2錶達,激活caspase-9、caspase-3誘導Eca-109細胞凋亡。
목적:탐토등리근(Actinidia arguta)을산을지제제촉진인식관암Eca-109세포조망적궤제。방법채용MTT비색법,검측등리근을산을지약액재불동농도(1μg/ml、10μg/ml、100μg/ml등)급불동시간(24h、48h、72h등)대Eca-109세포생장억제작용;채용TUNEL법검측기대암세포생장적유도조망효응;채용면역조화SP법,검측조망상관단백Bax 、Bcl-2급caspase적표체。결과등리근을산을지약액대인식관암Eca-109세포적생장억제작용,수착약물농도적승고화작용시간적연장이증강,기생장억제솔가체87.2%。등리근제제대류세포유명현적조망효응,이재대조조,미견유명현조망현상。류세포작용24h、48h、72h후분별여대조조비교,용약조Bax단백표체명현증강(P<0.01);동시반유Bcl-2표체감약,72h후최명현,차이유통계학의의(P<0.01)。등리근약액촉진caspase-3、caspase-9표체명현증강,이대caspase-8표체영향교소。결론등리근가통과하조Bcl-2표체,격활caspase-9、caspase-3유도Eca-109세포조망。
Objective To study the mechanism of Actinidia preparations on the apoptosis induction in human carcinoma of esophagus Eca-109 cells. Methods MTT colonmetric assay was used to examine the growth inhibition of concentration-effect(1μg/ml、10μg/ml、100μg/ml etc)and time-effect(24h、48h、72h etc)of extracts from Actinidia arguta by ethyl acetate on Eca-109 cells,TUNEL test were performed to observe the apoptosis induced by the extracts and the level of expression of Bax、Bcl-2 and caspase in tumor cells were measured by immunohistochemical method(SP technique). Results The inhibitory effect of the extracts from Actinidia arguta by ethyl acetate on Eca-109 cells increased step by step to concentration and time,the highest rate of inhibition was 87.2%. The extracts can significantly induced apoptosis of Eca-109 cells,but in control group,apoptosis was not observed. Compared with control group,the level of expression Bax in tumor cells increased(P<0.01),but the level of expression of Bcl-2 decreased after 24h、48h and 72h(P<0.01),particularly after 72h. The expressions of caspase-3 and caspase-9 were significantly enhanced by Actinidia arguta,but Little effect on caspase-8. Conclusions Actinidia arguta may induces apoptotic Eca-109 cells death through suppressing bcl-2 and then activating caspase-9 and caspase-3.