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Marine Benthic Cyanobacteria Contain Apoptosis-Inducing Activity Synergizing with Daunorubicin to Kill Leukemia Cells, but not Cardiomyocytes

机译:海洋底栖蓝细菌含有与柔红霉素协同杀伤白血病细胞但不杀伤心肌细胞的凋亡诱导活性。

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The potential of marine benthic cyanobacteria as a source of anticancer drug candidates was assessed in a screen for induction of cell death (apoptosis) in acute myeloid leukemia (AML) cells. Of the 41 marine cyanobacterial strains screened, more than half contained cell death-inducing activity. Several strains contained activity against AML cells, but not against non-malignant cells like hepatocytes and cardiomyoblasts. The apoptotic cell death induced by the various strains could be distinguished by the role of caspase activation and sensitivity to the recently detected chemotherapy-resistance-associated prosurvival protein LEDGF/p75. One strain (M44) was particularly promising since its activity counteracted the protective effect of LEDGF/p75 overexpressed in AML cells, acted synergistically with the anthracycline anticancer drug daunorubicin in AML cells, and protected cardiomyoblasts against the toxic effect of anthracyclines. We conclude that culturable benthic marine cyanobacteria from temperate environments provide a promising and hitherto underexploited source for novel antileukemic drugs.
机译:在对急性髓样白血病(AML)细胞诱导细胞死亡(细胞凋亡)的筛选中,评估了海洋底栖蓝细菌作为候选抗癌药物的潜力。筛选出的41种海洋蓝细菌菌株中,一半以上具有诱导细胞死亡的活性。几种菌株具有针对AML细胞的活性,但不具有针对非恶性细胞(如肝细胞和心肌母细胞)的活性。各种菌株诱导的凋亡细胞死亡可以通过caspase激活的作用和对最近检测到的与化疗耐药相关的生存蛋白LEDGF / p75的敏感性来区分。一种菌株(M44)特别有前景,因为其活性抵消了AML细胞中过表达的LEDGF / p75的保护作用,与AML细胞中的蒽环类抗癌药物柔红霉素协同作用,并保护了成心肌细胞免受蒽环类药物的毒性作用。我们得出的结论是,来自温带环境的可培养底栖海洋蓝细菌为新型抗白血病药物提供了有希望且迄今为止尚未得到充分利用的来源。

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