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Identification and Characterization of the Caspase-Mediated Apoptotic Activity of Teucrium mascatense and an Isolated Compound in Human Cancer Cells

机译:鉴定和半胱氨酸天牛和分离的化合物在人类癌细胞中的胱天蛋白酶介导的凋亡活性。

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摘要

Plants of the genus Teucrium (Lamiaceae or Labiatae family) are known historically for their medicinal value. Here, we identify and characterize the anticancer potential of T. mascatense and its active compound, IM60, in human cancer cells. The anti-proliferative effect of a T. mascatense methanol extract and its various fractions were analyzed in MCF-7 and HeLa cells in a dose- and time dependent manner. The dichloromethane fraction (TMDF) was observed to be the most effective with cytotoxicity against a more expanded series of cell lines, including MDA-MB-231. A time and dose-dependent toxicity profile was also observed for IM60; it could induce rapid cell death (within 3 h) in MCF-7 cells. Activation of caspases and PARP, hallmarks of apoptotic cell death pathways, following treatment with TMDF was demonstrated using western blot analysis. Inversion of the phosphatidylserine phospholipid from the inner to the outer membrane was confirmed by annexin V staining that was inhibited by the classical apoptosis inhibitor, Z-VAK-FMK. Changes in cell rounding, shrinkage, and detachment from other cells following treatment with TMDF and IM60 also supported these findings. Finally, the potential of TMDF and IM60 to induce enzymatic activity of caspases was also demonstrated in MCF-7 cells. This study, thus, not only characterizes the anticancer potential of T. mascatense, but also identifies a lead terpenoid, IM60, with the potential to activate anticancer cell death pathways in human cancer cells.
机译:Teucrium属(唇形科或唇形科)的植物在历史上因其药用价值而闻名。在这里,我们鉴定并鉴定了马斯卡特氏梭菌及其活性化合物IM60在人癌细胞中的抗癌潜力。在MCF-7和HeLa细胞中,以剂量和时间依赖性的方式分析了马斯卡特氏T甲醇提取物及其各种馏分的抗增殖作用。观察到二氯甲烷馏分(TMDF)对包括MDA-MB-231在内的更多系列细胞系具有最有效的细胞毒性。 IM60还观察到时间和剂量依赖性的毒性曲线;它可以诱导MCF-7细胞快速死亡(3小时内)。使用蛋白质印迹分析证实了TMDF处理后的半胱氨酸蛋白酶和PARP的激活,是凋亡细胞死亡途径的标志。膜联蛋白V染色证实了磷脂酰丝氨酸磷脂从内膜向外膜的转化,膜联蛋白V染色被经典的细胞凋亡抑制剂Z-VAK-FMK抑制。用TMDF和IM60处理后,细胞舍入,收缩和与其他细胞脱离的变化也支持了这些发现。最后,在MCF-7细胞中也证明了TMDF和IM60诱导胱天蛋白酶的酶活性的潜力。因此,这项研究不仅表征了雄性疟原虫的抗癌潜力,而且鉴定了萜烯类前体IM60,具有激活人类癌细胞中抗癌细胞死亡途径的潜力。

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