首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Persea declinata (Bl.) Kosterm Bark Crude Extract Induces Apoptosis in MCF-7 Cells via G0/G1 Cell Cycle Arrest Bcl-2/Bax/Bcl-xl Signaling Pathways and ROS Generation
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Persea declinata (Bl.) Kosterm Bark Crude Extract Induces Apoptosis in MCF-7 Cells via G0/G1 Cell Cycle Arrest Bcl-2/Bax/Bcl-xl Signaling Pathways and ROS Generation

机译:Persea declinata(Bl。)Kosterm树皮粗提取物通过G0 / G1细胞周期阻滞Bcl-2 / Bax / Bcl-xl信号通路和ROS产生诱导MCF-7细胞凋亡。

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摘要

Persea declinata (Bl.) Kosterm is a member of the Lauraceae family, widely distributed in Southeast Asia. It is from the same genus with avocado (Persea americana Mill), which is widely consumed as food and for medicinal purposes. In the present study, we examined the anticancer properties of Persea declinata (Bl.) Kosterm bark methanolic crude extract (PDM). PDM exhibited a potent antiproliferative effect in MCF-7 human breast cancer cells, with an IC50 value of 16.68 µg/mL after 48 h of treatment. We observed that PDM caused cell cycle arrest and subsequent apoptosis in MCF-7 cells, as exhibited by increased population at G0/G1 phase, higher lactate dehydrogenase (LDH) release, and DNA fragmentation. Mechanistic studies showed that PDM caused significant elevation in ROS production, leading to perturbation of mitochondrial membrane potential, cell permeability, and activation of caspases-3/7. On the other hand, real-time PCR and Western blot analysis showed that PDM treatment increased the expression of the proapoptotic molecule, Bax, but decreased the expression of prosurvival proteins, Bcl-2 and Bcl-xL, in a dose-dependent manner. These findings imply that PDM could inhibit proliferation in MCF-7 cells via cell cycle arrest and apoptosis induction, indicating its potential as a therapeutic agent worthy of further development.
机译:Persea declinata(Bl。)Kosterm是月桂科家族的成员,广泛分布于东南亚。它与鳄梨(Persea americana Mill)属同一属,鳄梨被广泛用作食品和药用。在本研究中,我们检查了Persea declinata(Bl。)Kosterm树皮甲醇粗提物(PDM)的抗癌特性。 PDM在MCF-7人乳腺癌细胞中表现出强大的抗增殖作用,治疗48小时后的IC50值为16.68µg / mL。我们观察到PDM导致细胞周期停滞并随后导致MCF-7细胞凋亡,这表现为G0 / G1期的种群增加,乳酸脱氢酶(LDH)释放更高和DNA片段化。机理研究表明,PDM引起ROS产生显着升高,从而导致线粒体膜电位,细胞通透性和caspases-3 / 7活化受到干扰。另一方面,实时PCR和蛋白质印迹分析表明,PDM处理以剂量依赖的方式增加了促凋亡分子Bax的表达,但降低了生存蛋白Bcl-2和Bcl-xL的表达。这些发现暗示PDM可以通过细胞周期停滞和凋亡诱导来抑制MCF-7细胞的增殖,表明其作为值得进一步发展的治疗剂的潜力。

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