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作 者:锁涛[1] 张涛[1] 童赛雄[1] 艾志龙[1] 刘厚宝[1] 秦新裕[1] 胡美玉[2] 王志军[2]
机构地区:[1]复旦大学附属中山医院外科,上海200032 [2]复旦大学附属中山医院实验研究中心,上海200032
出 处:《中华实验外科杂志》2010年第7期855-856,共2页Chinese Journal of Experimental Surgery
摘 要:目的 观察格尔德霉素(GA)对胆囊癌细胞生长、运动和侵袭的影响及其化疗增敏作用.方法 噻唑蓝(MTT)比色法检测(0、0.0064、0.032、0.16、0.8、4、20、100)×10-6 mol/L浓度梯度的GA对胆囊癌细胞GBC-SD生长影响;观察1 μmoL/L的GA对0.1倍最大血药浓度(Maximal plasma concentration,Cmax)的5-氟尿嘧啶(5-Fu,Cmax 10 mg/L)、丝裂霉素(MMC,Cmax 3 mg/L)、阿霉素(ADM,Cmax 0.4 mg/L)的化疗增敏作用.应用迁移运动及侵袭实验观察1μmol/L的GA体外对胆囊癌细胞运动、侵袭能力的影响.结果 GA体外对胆囊癌细胞有较强的抑制作用,半数抑制浓度(Inhibitory concentration 50%,IC50)在20μmol/L水平.1μmol/L低生长抑制浓度的GA能够增加传统化疗药物对GBC-SD生长的抑制作用,有明显的增效作用;同时低浓度的GA可以抑制肝细胞生长因子(HGF)对GBC-SD运动迁移和侵袭能力的诱导作用.结论 GA有可能成为胆囊癌化疗和抗转移的有效药物.Objective To study the effects of Geldanamycin (GA) on the proliferation, motility and invasion of gallbladder carcinoma (GBC) cells and its synergistic effects with S-Fu, ADM and MMC in vitro. Methods Methyl thiazolyl tetrazolium(MTT) assays were used to investigate the effects of GA [(0,0.0064,0.032,0.16,0.8,4,20, 100)×10-6 mol/L] on the proliferation of GBC-SD. The enhanced antitumor activities of 5-Fu (Cmax 10 mg/L) , MMC (Cmax 3 mg/L) and ADM (Cmax 0.4 mg/L) at 0.1 × Cmax were observed in combination with GA at 1 μmol/L (a very low cytotoxic concentration). Motility and invasion abilities were tested to evaluate the inhibitory effects of GA at 1 μmol/L. Results In MTT assays, GA could inhibit growth of cancer cells sharply at the concentration of 20 μmol/L (IC50). Although it couldn't postpone the motility and invasion apparently by itself, GA at 1 μmol/L could inhibit the HGF/SF-mediated increase of motility and invasion. The enhanced antitumor activity of 5-Fu, MMC and ADM was observed in combination with GA at 1 μmol/L The synergistic effects were very significant. Conclusion GA may be potent agents to inhibit development and metastasis of GBC in the near future.
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