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Nujiangexathone A, a Novel Compound Derived from Garcinia nujiangensis , Induces Caspase-Dependent Apoptosis in Cervical Cancer through the ROS/JNK Pathway

机译:怒江藤黄酮A(一种来自怒江藤黄的新型化合物)通过ROS / JNK途径诱导宫颈癌中胱天蛋白酶依赖性凋亡。

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Nujiangexathone A (NJXA), a novel compound derived from Garcinia nujiangensis , has been demonstrated to inhibit the proliferation of several human cancer cell lines. This study is the first to demonstrate the apoptosis inductive activities of NJXA and the possible underlying mechanisms. Our results demonstrated that NJXA inhibited colony formation by HeLa and SiHa cells in a dose-dependent manner. An Annexin V-FITC/PI staining assay showed that NJXA strongly triggered apoptosis in a dose-dependent manner. Western blotting analyses showed that NJXA induced the caspase-dependent apoptosis of HeLa and SiHa cells by triggering a series of events, including changes in the levels of Bcl-2 family proteins, cytochrome c release, caspase-3 activation, and chromosome fragmentation. Furthermore, we demonstrated that NJXA induced cell apoptosis by activating the reactive oxygen species (ROS)-mediated JNK signaling pathway. Consistent with this finding, a ROS scavenger, N -acetyl- l -cysteine (NAC, 10 mM), hindered NJXA-induced apoptosis and attenuated the sensitivity of HeLa and SiHa cells to NJXA. In vivo results further confirmed that the tumor inhibitory effect of NJXA was partially through the induction of apoptosis. Taken together, our results demonstrated that NJXA induced the apoptosis of HeLa and SiHa cells through the ROS/JNK signaling pathway, indicating that NJXA could be important candidate for the clinical treatment of cervical cancer.
机译:Nujiangexathone A(NJXA)是一种源自怒江藤黄的新型化合物,可抑制多种人类癌细胞系的增殖。这项研究是首次证明NJXA的凋亡诱导活性及其可能的潜在机制。我们的结果表明,NJXA以剂量依赖性方式抑制HeLa和SiHa细胞的集落形成。 Annexin V-FITC / PI染色试验表明,NJXA以剂量依赖性方式强烈触发细胞凋亡。蛋白质印迹分析表明,NJXA通过触发一系列事件(包括Bcl-2家族蛋白水平的变化,细胞色素c的释放,caspase-3的活化和染色体片段化)诱导了HeLa和SiHa细胞的caspase依赖性凋亡。此外,我们证明了NJXA通过激活活性氧(ROS)介导的JNK信号通路来诱导细胞凋亡。与该发现一致的是,ROS清除剂N-乙酰基-1-半胱氨酸(NAC,10 mM)阻碍了NJXA诱导的凋亡,并减弱了HeLa和SiHa细胞对NJXA的敏感性。体内结果进一步证实了NJXA的肿瘤抑制作用部分是通过诱导细胞凋亡。综上所述,我们的结果表明NJXA通过ROS / JNK信号通路诱导HeLa和SiHa细胞凋亡,表明NJXA可能是宫颈癌临床治疗的重要候选药物。

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