首页> 外文会议>2007 IEEE/ICME INTERNATIONAL CONFERENCE ON COMPLEX MEDICAL ENGINEERING >Ursolic Acid Accelerates Taxol-induced Apoptosis via Activation of Bid-Mitochondria-Cyto c Signaling Pathway
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Ursolic Acid Accelerates Taxol-induced Apoptosis via Activation of Bid-Mitochondria-Cyto c Signaling Pathway

机译:熊果酸通过激活线粒体-Cyc信号通路促进紫杉醇诱导的细胞凋亡。

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Taxol triggers apoptosis in a variety of cancer cell types and activated NF-κB is regarded as a main reason to cancer cells resistance to Taxol-induced apoptosis. Ursolic acid, a natural component, can inhibit activation of NF-κB in many apoptosis stimulus, such as TNF, cispatin. In order to find synergistic effect between Taxol and ursolic acid, plasmid pFRET-Bid, pE-GFP-Cyt-c, and pDsRed-Mit were used to dynamically monitor cleavage of Bid, and cytochrome c release from mitochondria in Taxol alone and combination treatment of Taxol and ursolic acid. In Taxol alone, Bid was not cleaved and cytochrome c was not released from mitochondria in ASTC-a-1 cells, however, cleavage of Bid and release of cytochrome c from mitochondria were observed in combination treatment of Taxol and ursolic acid, so we predicted that activation of Bid-Mitochodria-Cyto c signaling pathway might contribute to the enhancement of Taxol-induced apoptosis with ursolic acid during combination treatment. Furthermore, Taxol-induced apoptosis in ASTC-a-1 cells may be mainly dependent on intrinsic apoptosis pathway, and mitochondria may mediate apoptosis speed.
机译:紫杉醇触发多种癌细胞类型的凋亡,而活化的NF-κB被认为是癌细胞对紫杉醇诱导的凋亡产生抗性的主要原因。熊果酸是一种天然成分,可以抑制许多细胞凋亡刺激物中的NF-κB活化,例如TNF,顺铂。为了发现紫杉醇和熊果酸之间的协同作用,使用质粒pFRET-Bid,pE-GFP-Cyt-c和pDsRed-Mit动态监测Bid的裂解,单独使用紫杉醇和联合治疗可从线粒体释放细胞色素c。紫杉醇和熊果酸。仅在紫杉醇中,ASTC-a-1细胞中的Bid不会被切割,线粒体中不会释放细胞色素c,但是,在紫杉醇和熊果酸的联合治疗中观察到了Bid的切割和线粒体中细胞色素c的释放,因此我们预测Bid-线粒体-Cyto c信号转导通路的激活可能有助于在联合治疗过程中用乌索酸增强紫杉醇诱导的细胞凋亡。此外,紫杉醇诱导的ASTC-a-1细胞凋亡可能主要取决于内在的凋亡途径,而线粒体可能介导凋亡的速度。

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