首页> 美国卫生研究院文献>International Journal of Oncology >Epoxymicheliolide a novelguaiane-type sesquiterpene lactone inhibits NF-κB/COX-2 signaling pathways by targeting leucine 281 and leucine 25 in IKKβ in renal cell carcinoma
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Epoxymicheliolide a novelguaiane-type sesquiterpene lactone inhibits NF-κB/COX-2 signaling pathways by targeting leucine 281 and leucine 25 in IKKβ in renal cell carcinoma

机译:新型环氧类倍半萜内酯环氧米奇内酯通过靶向肾癌中IKKβ中的亮氨酸281和亮氨酸25来抑制NF-κB/ COX-2信号通路

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摘要

Parthenolide (PTL) is a sesquiterpene lactone compound obtained from Tanacetum parthenium (feverfew) and inhibits the activation of nuclear factor (NF)-κB. Epoxymicheliolide (EMCL) is a compound which is structurally related to PTL; however, EMCL is more stable under acidic and alkaline conditions. As a biologically active molecule, the detailed mechanism by which EMCL inhibits tumor activity remains to be elucidated. The present study evaluated the effect of EMCL on renal cell carcinoma (RCC) cells and identified the underlying mechanisms. It was found that treatment with EMCL significantly inhibited the proliferation of RCC cells in vitro and increased the induction of apoptosis by activating the mitochondria- and caspase-dependent pathway. Simultaneously, EMCL suppressed cell invasion and metastasis by inhibiting epithelial-mesenchymal transition, as observed in a microfluidic chip assay. Furthermore, using immunofluorescence analysis, an electrophoretic mobility shift assay and a dual-luciferase reporter assay, it was shown that treatment with EMCL significantly suppressed the expression of cyclooxygenase-2 by inhibiting the translocation of NF-κB p50/p65 and the activity of NF-κB. Collectively, the results indicated that EMCL suppressed tumor growth by inhibiting the activation of NF-κB and suggested that EMCL may be a novel anticancer agent in the treatment of RCC.
机译:爬山酚(PTL)是从单叶艾菊(feverfew)获得的倍半萜烯内酯化合物,可抑制核因子(NF)-κB的活化。环氧米奇内酯(EMCL)是与PTL结构相关的化合物;但是,EMCL在酸性和碱性条件下更稳定。作为一种生物活性分子,EMCL抑制肿瘤活性的详细机理尚待阐明。本研究评估了EMCL对肾细胞癌(RCC)细胞的影响并确定了潜在的机制。发现用EMCL处理在体外显着抑制RCC细胞的增殖,并通过激活线粒体和胱天蛋白酶依赖性途径增加凋亡的诱导。同时,EMCL通过抑制上皮间质转化来抑制细胞侵袭和转移,如在微流控芯片检测中所观察到的。此外,使用免疫荧光分析,电泳迁移率变动分析和双荧光素酶报告基因分析表明,EMCL处理通过抑制NF-κBp50 / p65的易位和NF活性显着抑制了环氧合酶-2的表达。 -κB。总体而言,该结果表明EMCL通过抑制NF-κB的活化来抑制肿瘤的生长,并表明EMCL可能是RCC治疗中的一种新型抗癌药。

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