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Autophagy Interplay with Apoptosis and Cell Cycle Regulation in the Growth Inhibiting Effect of Resveratrol in Glioma Cells

机译:自噬与细胞凋亡和细胞周期调控相互作用在白藜芦醇对胶质瘤细胞生长的抑制作用。

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摘要

Prognosis of patients with glioblastoma (GBM) remains very poor, thus making the development of new drugs urgent. Resveratrol (Rsv) is a natural compound that has several beneficial effects such as neuroprotection and cytotoxicity for several GBM cell lines. Here we evaluated the mechanism of action of Rsv on human GBM cell lines, focusing on the role of autophagy and its crosstalk with apoptosis and cell cycle control. We further evaluated the role of autophagy and the effect of Rsv on GBM Cancer Stem Cells (gCSCs), involved in GBM resistance and recurrence. Glioma cells treated with Rsv was tested for autophagy, apoptosis, necrosis, cell cycle and phosphorylation or expression levels of key players of these processes. Rsv induced the formation of autophagosomes in three human GBM cell lines, accompanied by an upregulation of autophagy proteins Atg5, beclin-1 and LC3-II. Inhibition of Rsv-induced autophagy triggered apoptosis, with an increase in Bax and cleavage of caspase-3. While inhibition of apoptosis or autophagy alone did not revert Rsv-induced toxicity, inhibition of both processes blocked this toxicity. Rsv also induced a S-G2/M phase arrest, accompanied by an increase on levels of pCdc2(Y15), cyclin A, E and B, and pRb (S807/811) and a decrease of cyclin D1. Interestingly, this arrest was dependent on the induction of autophagy, since inhibition of Rsv-induced autophagy abolishes cell cycle arrest and returns the phosphorylation of Cdc2(Y15) and Rb(S807/811), and levels of cyclin A, and B to control levels. Finally, inhibition of autophagy or treatment with Rsv decreased the sphere formation and the percentage of CD133 and OCT4-positive cells, markers of gCSCs. In conclusion, the crosstalk among autophagy, cell cycle and apoptosis, together with the biology of gCSCs, has to be considered in tailoring pharmacological interventions aimed to reduce glioma growth using compounds with multiple targets such as Rsv.
机译:胶质母细胞瘤(GBM)患者的预后仍然很差,因此迫切需要开发新药。白藜芦醇(Rsv)是一种天然化合物,对多种GBM细胞系具有多种有益作用,例如神经保护和细胞毒性。在这里,我们评估了Rsv对人GBM细胞系的作用机制,重点是自噬的作用及其与细胞凋亡和细胞周期控制的串扰。我们进一步评估了自噬的作用和Rsv对GBM癌症干细胞(gCSCs)的影响,涉及GBM耐药性和复发。测试了用Rsv处理的胶质瘤细胞的自噬,细胞凋亡,坏死,细胞周期以及这些过程中关键分子的磷酸化或表达水平。 Rsv诱导了三种人类GBM细胞系中自噬体的形成,并伴有自噬蛋白Atg5,beclin-1和LC3-II的上调。 Rsv诱导的自噬的抑制触发细胞凋亡,增加Bax和caspase-3的裂解。虽然单独抑制细胞凋亡或自噬并不能恢复Rsv诱导的毒性,但同时抑制这两种过程都可以阻断这种毒性。 Rsv还诱导了S-G2 / M期阻滞,伴随着pCdc2(Y15),细胞周期蛋白A,E和B和pRb(S807 / 811)的水平增加以及细胞周期蛋白D1的降低。有趣的是,这种抑制依赖于自噬的诱导,因为抑制Rsv诱导的自噬消除了细胞周期的阻滞,使Cdc2(Y15)和Rb(S807 / 811)的磷酸化以及细胞周期蛋白A和B的水平得以控制水平。最后,自噬的抑制或Rsv的处理降低了球的形成以及gCSC的标志物CD133和OCT4阳性细胞的百分比。总之,自噬,细胞周期和细胞凋亡之间的相互影响,以及gCSC的生物学特性,在使用多种靶标化合物(例如Rsv)定制旨在减少神经胶质瘤生长的药理干预措施时,必须加以考虑。

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