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作 者:刘宗潮[1] 谢冰芬[1] 潘启超[1] 苏秀容[1] 冯公侃[1] 王理开[1] 张润梅[1] 张宏达[1]
机构地区:[1]中山医科大学肿瘤研究所,中山医科大学生物化学教研室,中山大学生物系植物研究室
出 处:《癌症》1996年第3期164-167,共4页Chinese Journal of Cancer
基 金:中央卫生部科学基金
摘 要:应用噻唑兰(MTT)法测得毛叶茶提取物(ECPC)对人肝癌细胞(BEL-7402)的半数抑制浓度(IC_(50))为351.1μg/ml;台盼蓝拒染法(TBE)的IC_(50)为115.2μg/ml;用MTT法测得ECPC对人红白血病细胞(K_(562))的IC_(50)>1000μg/ml,TBE法测得其对K_(562)细胞的IC_(50)为81.4μg/ml。ECPC对人胎儿肺纤维细胞(HFLF)和人胎儿肾细胞(HFK)显示促生长作用。在药物浓度为62.5、125.0、250.0、500.0和1000.0μg/ml的培养下,对HFLF细胞的生长促进率分别为—10.47、+15.48、+31.91、+53.02和+83.37%:对HFK细胞的生长促进率分别为+14.18、+26.61、+52.62、+88.13和+103.71%。FCPC分别与阿糖胞苷(Ara—C)、环磷酰胺(CTX)和阿霉素(ADM)合用对网织细胞肉瘤(L_2)的抑瘤率高于各个单药的抑瘤率。加用ECPC后Ara—C可从单用平均抑瘤率38.2%升高到64%;CTX从平均31.3%升高到48.9%;ADM从平均15.2%升高到45.5%,q?The cytotoxic effect of extract of Camellia ptilophylla Chang(ECPC)on human hepatic can-cer cell line(BEL-7402)and human erythroleukemia cell line(K562)was determined using MTT assaymethod and tyrpan blue exclusion method(TBE).The IC50 of ECPC against BEL-7402 cells was calculat-ed to be 351.1μg/ml using MTT assay and 115.2 μg/ml using TBE assay. The IC50 against K562 cells wasover 1,000 μg/ml using MTT assay and 81.4μg/ml using TBE assay. While ECPC on human fetus lung fi-brocyte(HFLF)and human fetus kidney cells(HFK)showed growth promotion effect.Under the concen-tration of ECPC of 62.5,250.500 and 1,000g/ml,the growth promotion rates on HFLF were -10. 47,+15.48,+ 31.91,+ 53.02 and + 83.37%,respectively,The growth promotion rates of ECPC on HFKwere + 14.18,+ 26.61,+ 52.62,+ 88. 13 and + 103.71 %. The inhibitory rates of the combination of ECPC with Ara -C or CTX or ADM against L2 in mice werehigher than those of respective single drug. The average inhibitory rates(IR)of Ara -C after addition of ECPC was increased from 38.2% to 64%. The IR of CTX after addition of ECPC was increased from31.3% to 48.9%,and the IR for ADM from 15.2% to 45.5%,q all > 1,showing that the combination ofECPC with these drugs could enhance the antitumor effect.In human nasopharyngeal cancer cells(CNE2)treated by ECPC of concentration of 125-500 μg/ ml DNA breakage was induced.The degree of DNAbreakage increased with increasing concentration of ECPC.
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