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作 者:吴炎鹏[1] 许卫兵[2] 贾凌云[1] 孔花青[1] 丁兰[1] 何苗[1] 刘国安[1] 杨红[1]
机构地区:[1]西北师范大学生命科学学院、天然产物与抗癌分子药理学实验室,兰州730070 [2]西北师范大学化学化工学院、甘肃省高分子重点实验室,兰州730070
出 处:《中国科学:生命科学》2014年第5期471-480,共10页Scientia Sinica(Vitae)
基 金:国家自然科学基金(批准号:30960464);西北师范大学“知识与科技创新工程”项目(批准号:NWNU-KJCXGC-03-65)资助
摘 要:以N-(2-羟丙基)甲基丙烯酰胺(HPMA),N-(3-氨基丙基)甲基丙烯酰胺(APMA)和金反式维甲酸(ATRA)为原料,采用自由基溶液聚合法设计合成P(HPMA-APMA).ATRA,并用核磁共振氢谱对该化合物进行结构表征.相比于单体ATRA,聚合物的水溶性显著增加,同时可通过胞吞作用进入细胞.3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐(MTT)法评估聚合物和单体ATRA对人早幼粒白血病细胞HL-60生长的抑制作用,流式细胞术检测两者对HL-60细胞周期分布及细胞表面抗原CDllb表达的影响,进一步结合氯化硝基四氮唑蓝(NBT)还原法评估聚合物诱导HL-60细胞分化的能力.结果显示,聚合物比单体ATRA具有更强的细胞生长抑制活性,其IC_50值分别为1.03和4.09μmol/L;聚合物还具有更高的G_0/G_1期细胞阻滞效应,1.2μmol/L时,聚合物比单体ATRA的G_0/G_1期细胞率高出17.7%;同样,0.4μmol/L聚合物与2.4μmaol/L单体ATRA诱导HL-60的NBT还原能力相当,0.8μmaol/L聚合物与2.4μmol/L单体ATRA诱导HL-60细胞表面抗原CDllb表达相当,表明聚合物比单体ATRA具有更强的诱导HL-60细胞向粒细胞分化的能力,其药效增强3~4倍.P(HPMA-APMA)-ATRA was synthesized by free-radical solution polymerization with N-(2-hydroxypropyl methacrylamide) (HPMA), N-(3-aminopropyl) methacrylamide (APMA) and all-trans retinoic acid (ATRA) as raw materials. The structure of the polymer was confirmed by 1H NMR. Compared with the monomeric ATRA, the water-solubility of the polymer increased significantly and could enter the cells through endocytosis. The inhibition of polymerized and monomeric ATRA on HL-60 cell growth was assessed by MTT(3-(4,5-dimethylthiazol- 2-yl)-2,5-diphenyl-tetrazolium bromide). Then flow cytometry was used to detect the effects of the two compounds on cell cycle distribution and expression of cell surface antigen CDllb in HL-60 cell. Finally, a further experiment with NBT (nitroblue tetrazolium) was conducted to analyze the cell differentiation of HL-60 induced by the two compounds. The P-ATRA showed a stronger suppressive ability on cell growth than monomeric ATRA, the IC50 was 1.03 and 4.09 μmol L-1, respectively. The P-ATRA had a higher G0/G1 phase cell block effect. At the concentration of 1.2 μmol L-1, G0/G1 phase cell rate induced by P-ATRA was 17.7% higher than that of monomeric ATRA. The NBT reduction ability of HL-60 induced by 0.4 μmol L-1 P-ATRA was similar with that of 2.4 μmol L-: ATRA, the expression of cell surface antigen CD1 lb in HL-60 cell induced by 0.8 μmol L-1 P-ATRA was similar with that of 2.4 μmol L-1 ATRA, and the results indicated that the differentiation of HL-60 cell induced by P-ATRA increased 3-4 folds compared to that of ATRA.
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