Mahdavi Majid, Yazdanparast Razieh
Institute of Biochemistry and Biophysics, P.O. Box. 13145-1384, University of Tehran, Tehran, Iran.
Arch Pharm Res. 2007 Feb;30(2):177-81. doi: 10.1007/BF02977692.
Gnidilatimonoein is a new diterpene ester, recently isolated from the leaves of Daphne macronata with potent anti-tumoral and anti-metastastic activities (Yazdanparast et al., 2004). Promyeloblastic (KG1), promyelocytic (NB4) and promonocytic (U937) cells were cultured in the presence of various concentrations of the drug (0.5-3.0 microM) for 3 days. Herein, we report that gnidilatimonoein induces differentiation and apoptosis in KG1, NB4 and U937 cells. The drug inhibited growth and proliferation of KG1, NB4 and U937 cells with IC50 values of 1.5, 1.5 and 1.0 microM, respectively, after 72 h of treatment. Cell viability was also decreased by 18%, 20% and 23%, respectively, after 72 h treatment with the drug. NBT reducing assay revealed that the inhibition of proliferation is associated with differentiation especially toward monocytes-like morphology. Indeed, the drug at 0.5-1.5 microM induced differentiation by 5-50% in the cells. Acridine orange/ethidium bromide (AO/EtBr) double staining and DNA fragmentation assays revealed that apoptosis occurred after differentiation of the cells. Based on the present data, it seems that the new compound is a good candidate for further evaluation as an effective chemotherapeutic agent acting through induction of differentiation and apoptosis.
狼毒大戟单萜酯是一种新的二萜酯,最近从狼毒大戟的叶子中分离出来,具有很强的抗肿瘤和抗转移活性(亚兹丹帕斯特等人,2004年)。早幼粒细胞(KG1)、早幼粒细胞(NB4)和单核细胞(U937)细胞在不同浓度的药物(0.5 - 3.0微摩尔)存在下培养3天。在此,我们报告狼毒大戟单萜酯可诱导KG1、NB4和U937细胞分化和凋亡。处理72小时后,该药物抑制KG1、NB4和U937细胞的生长和增殖,其IC50值分别为1.5、1.5和1.0微摩尔。用该药物处理72小时后,细胞活力也分别下降了18%、20%和23%。硝基蓝四唑还原试验表明,增殖的抑制与分化相关,尤其是向单核细胞样形态的分化。事实上,0.5 - 1.5微摩尔的药物可诱导细胞分化5% - 50%。吖啶橙/溴化乙锭(AO/EtBr)双重染色和DNA片段化分析表明,细胞分化后发生凋亡。基于目前的数据,这种新化合物似乎是一种很好的候选药物,可作为一种通过诱导分化和凋亡起作用的有效化疗药物进行进一步评估。
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