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Limonoid compounds from Xylocarpus granatum and their anticancer activity against esophageal cancer cells

机译:来自Xylocarpus Granatum的柠檬气化合物及其对食管癌细胞的抗癌活性

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BACKGROUND:To investigate the anticancer effects of limonoid compounds that were isolated and purified from Xylocarpus granatum fruits on human esophageal cancer (EC) cells. A structure-activity relationship experiment was designed to identify the functional moiety of limonoid compounds identified as being critical for its anticancer activity.METHODS:Eca109 cells were cultured in RPMI1640 medium and treated with limonoid compounds. Cell proliferation was determined by the MTT assay in vitro. Eca109 cells apoptosis was analyzed by by flow cytometry after being treated with xylogranatin C. The expression of p53, Bax, bcl-2, caspase-3 and GRP78 in Eca109 cells after xylogranatin C treatment was examined by western blot assay.RESULTS:Four linonoid compounds strongly inhibited the cellular proliferation of Eca109 cells. Xylogranatin C was the strongest inhibitor, whose inhibitory effect was comparable to that of the well-known chemotherapeutic agent, cisplatin. Furthermore, xylogranatin C might induce Eca109 cell apoptosis through joint effects on multiple pathways, including the death receptor and endoplasmic reticulum pathways. Additionally, xylogranatin C suppressed tumor cell proliferation by upregulating miR-203a expression in Eca109 cells.CONCLUSIONS:Xylogranatin C induced Eca109 cellular apoptosis and exerted antitumor activity. Xylogranatin C suppressed tumor cell proliferation by upregulating miR-203a expression in Eca109 cells.? 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:背景:探讨柠檬糖化合物的抗癌效果被隔离和纯化的人食管癌(EC)细胞上的Xylocarpus Granatum果实中分离和纯化。设计了一种结构 - 活性关系实验,鉴定鉴定为其抗癌活性至关重要的柠檬糖化合物的功能部分。方法:在RPMI1640培养基中培养ECA109细胞并用柠檬烷化合物处理。细胞增殖由MTT测定体体外测定。通过流式细胞术在用Xaltogranatin C处理后通过流式细胞术分析ECA109细胞凋亡。通过Western Blot Assay检查了Xylogranatin C治疗后ECA109细胞中P53,Bax,Bcl-2,Caspase-3和Grp78的表达。结果:四种碱硬质化合物强烈抑制了ECA109细胞的细胞增殖。 Xylogranatin C是最强的抑制剂,其抑制作用与众所周知的化学治疗剂,顺铂相当。此外,Xylogranatin C可以通过对多种途径的关节作用来诱导ECA109细胞凋亡,包括死亡受体和内质网途径。另外,Xylogranatin C通过上调ECA109细胞中的miR-203a表达来抑制肿瘤细胞增殖。结论:Xylogranatin C诱导ECA109细胞凋亡并施加抗肿瘤活性。 Xylogranatin C通过上调ECA109细胞中的miR-203a表达抑制肿瘤细胞增殖。? 2020作者。中国肺部肿瘤集团和约翰瓦里和儿子澳大利亚发表的胸癌

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