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作 者:李星[1] 马刘江[2] 玄永哲[2] 安京华[2] 李香善[2] 石俊[2]
机构地区:[1]首都医科大学燕京医学院附属北京大兴医院急诊科,102600 [2]吉林省延边大学附属医院延吉,ICU133000
出 处:《中华临床营养杂志》2012年第1期30-32,共3页Chinese Journal of Clinical Nutrition
基 金:国家自然科学基金项目(30560152)及吉林省教育厅项目[吉教科合字(2008)第18号]
摘 要:目的观察廿烷五烯酸(EPA)单剂以及与卡铂联合应用对人肺腺癌A-549细胞系增殖和凋亡的影响。方法分别用100μg/ml卡铂、80μg/mlEPA以及100μg/ml卡铂联合80μg/mlEPA孵育A-549细胞48h后,采用MTr法检测药物对h-549细胞增殖的抑制率,HE染色观察细胞形态学,流式细胞术定量分析细胞凋亡率。结果100μg/ml卡铂联合80μg/mlEPA对A-549细胞系的增殖抑制率为85.20%±5.00%,显著高于80μg/mlEPA(32.85%±3.00%,P=0.0001)或100μg/ml卡铂(53.25%±3.00%,P=0.0013)单独的作用。HE染色显示:药物干预后部分A-549细胞出现凋亡形态学改变。卡铂联合EPA组A-549细胞凋亡率为17.05%4-4.00%,显著高于单用卡铂组(9.49%±1.00%,P20.0252)。结论EPA可能具有增强卡铂抑制人肺腺癌A-549细胞系增殖、促进A-549细胞系凋亡的作用。Objective To investigate the effects of eicosapentaenoic acid (EPA) or EPA plus carboplatin on the proliferation and apoptosis of human lung cancer cell line A-549. Methods A-549 cells were cultured by 100 μg/ml carboplatin, 80 μg/ml EPA, and their combination for 48 hours. MTT assay was used to determine the effect of EPA, carboplatin, or their combination on the proliferation of human lung cancer cell line A-549. The morphological changes of human lung cancer cell line A-549 were observed using HE staining, and apoptosis of A-549 cells was analyzed by flow cytometry. Results MTT assay showed that the proliferation inhibition rate of A-549 cells cultured with EPA plus carboplatin was 85.20% ± 5.00%, which was significantly higher than that of cells cultured with 80 ug/ml EPA (32. 85% ± 3.00%, P = 0. 0001 ) or 100 ug/ml carboplatin (53.25%±3.00%, P = 0.0013 ). HE staining showed apoptosis in all three groups, whereas the apoptosis rate reached 17.05% ± 4.00% in the combination group, which was significantly higher than that in carboplatin group (9.49% ± 1.00% , P =0. 0252). Conclusion EPA may enhance the effects of carboplatin in inhibiting the proliferation and promoting the apoptosis of human lung cancer cell line A-549.
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