首页> 外文期刊>Drug Design, Development and Therapy >Liriodenine, an aporphine alkaloid from -Enico-santhellum pulchrum, inhibits proliferation of?human ovarian cancer cells through induction of apoptosis via the mitochondrial signaling pathway and blocking cell cycle progression
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Liriodenine, an aporphine alkaloid from -Enico-santhellum pulchrum, inhibits proliferation of?human ovarian cancer cells through induction of apoptosis via the mitochondrial signaling pathway and blocking cell cycle progression

机译:鹅绒烯碱是一种来自-Enico-santhellum的磷的生物碱,通过线粒体信号传导途径诱导凋亡并阻止细胞周期进程,从而抑制人卵巢癌细胞的增殖

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Abstract: Enicosanthellum pulchrum is a tropical plant from Malaysia and belongs to the Annonaceae family. This plant is rich in isoquinoline alkaloids. In the present study, liriodenine, an isoquinoline alkaloid, was examined as a potential anticancer agent, particularly in ovarian cancer. Liriodenine was isolated by preparative high-performance liquid chromatography. Cell viability was performed to determine the cytotoxicity, whilst the detection of morphological changes was carried out by acridine orange/propidium iodide assay. Initial and late apoptosis was examined by Annexin V-fluorescein isothiocyanate and DNA laddering assays, respectively. The involvement of pathways was detected via caspase-3, caspase-8, and caspase-9 analyses. Confirmation of pathways was further performed in mitochondria using a cytotoxicity 3 assay. Apoptosis was confirmed at the protein level, including Bax, Bcl-2, and survivin, while interruption of the cell cycle was used for final validation of apoptosis. The result showed that liriodenine inhibits proliferation of CAOV-3 cells at 37.3 μM after 24 hours of exposure. Changes in cell morphology were detected by the presence of cell membrane blebbing, chromatin condensation, and formation of apoptotic bodies. Early apoptosis was observed by Annexin V-fluorescein isothiocyanate bound to the cell membrane as early as 24 hours. Liriodenine activated the intrinsic pathway by induction of caspase-3 and caspase-9. Involvement of the intrinsic pathway in the mitochondria could be seen, with a significant increase in mitochondrial permeability and cytochrome c release, whereas the mitochondrial membrane potential was decreased. DNA fragmentation occurred at 72 hours upon exposure to liriodenine. The presence of DNA fragmentation indicates the CAOV-3 cells undergo late apoptosis or final stage of apoptosis. Confirmation of apoptosis at the protein level showed overexpression of Bax and suppression of Bcl-2 and survivin. Liriodenine inhibits progression of the CAOV-3 cell cycle in S phase. These findings indicate that liriodenine could be considered as a promising anticancer agent.
机译:摘要:Enicosanthellum pulchrum是马来西亚的一种热带植物,隶属于番荔枝科。该植物富含异喹啉生物碱。在本研究中,异丁喹啉生物碱鹅绒素被作为一种潜在的抗癌剂,特别是在卵巢癌中。通过制备型高效液相色谱法分离出鹅绒素。进行细胞生存力以确定细胞毒性,同时通过a啶橙/碘化丙啶测定法进行形态变化的检测。分别通过膜联蛋白V-异硫氰酸荧光素和DNA阶梯分析检测初始和晚期细胞凋亡。通过caspase-3,caspase-8和caspase-9分析检测了途径的参与。使用细胞毒性3试验进一步在线粒体中进行通路的确认。在包括Bax,Bcl-2和survivin在内的蛋白质水平上证实了细胞凋亡,而中断细胞周期用于细胞凋亡的最终验证。结果表明,暴露24小时后,鹅绒den碱可抑制CAOV-3细胞的增殖,浓度为37.3μM。通过细胞膜起泡,染色质浓缩和凋亡小体的存在来检测细胞形态的变化。膜联蛋白V-荧光素异硫氰酸酯在细胞膜上的结合最早可在24小时时观察到。 Liriodenine通过诱导caspase-3和caspase-9激活内在途径。可以观察到内在途径参与线粒体,线粒体通透性和细胞色素c释放显着增加,而线粒体膜电位降低。 DNA片段在暴露于liriodenine的72小时后发生断裂。 DNA片段的存在表明CAOV-3细胞经历了晚期凋亡或凋亡的最后阶段。在蛋白质水平上的细胞凋亡的证实显示Bax的过度表达和Bcl-2和survivin的抑制。 Liriodenine抑制S期CAOV-3细胞周期的进展。这些发现表明,鹅绒素可以被认为是有前途的抗癌药。

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