赫拉
细胞凋亡
活性氧
DNA断裂
膜联蛋白
细胞色素c
化学
细胞生物学
分子生物学
MTT法
碎片(计算)
半胱氨酸蛋白酶8
半胱氨酸蛋白酶
程序性细胞死亡
生物
细胞
生物化学
生态学
作者
Li Zhang,Siyuan Kong,Zhaoqing Zheng,Xiaoxiao Meng,Jiling Feng,Hongsheng Tan,Yuanzhi Lao,Lianbo Xiao,Hong‐Xi Xu
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2016-10-12
卷期号:21 (10): 1360-1360
被引量:10
标识
DOI:10.3390/molecules21101360
摘要
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.
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