MAPK/ERK通路
细胞凋亡
化学
细胞色素c
血管生成
基质金属蛋白酶
细胞毒性
倍半萜
半胱氨酸蛋白酶
激酶
STAT蛋白
倍半萜内酯
车站3
生物化学
信号转导
癌症研究
生物
程序性细胞死亡
立体化学
体外
作者
Nguyen Hoai Nguyen,Minh Tan Nguyen,Peter J. Little,Anh Thư,Phuong Trinh Tran,Nam Xuan Vo,Bich Hang
出处
期刊:Journal of Environmental Pathology Toxicology and Oncology
[Begell House Inc.]
日期:2020-01-01
卷期号:39 (4): 299-308
被引量:7
标识
DOI:10.1615/jenvironpatholtoxicoloncol.2020034066
摘要
Vernolide-A and vernodaline are sesquiterpene lactones isolated from genera of Vernonia. Vernolide-A and vernodaline have shown promising therapeutic properties, including antibacterial, antihelminth, and antioxidant activities. Recently, the anticancer properties of these sesquiterpene lactones have been investigated with the elucidation of effects on cell proliferation, metastasis, angiogenesis, and apoptosis. The antiproliferation and antimetastatic activities arise from targeting extracellular signal-regulated kinase 1 (ERK-1), extracellular signal-regulated kinase 2 (ERK-2), nuclear factor-κB (NF-κB), signal transducer and activator of transcription 3 (STAT3), matrix metalloproteinase 2 (MMP-2), and matrix metalloproteinase 9 (MMP9). The induction of apoptosis is due to the enhancement of caspase 9, caspase 3, while inhibition of Bcl-2 and Bcl-xL results in the release of cytochrome c into the cytosol. The activity of vernolide-A and vernodaline is hypothesized to be due to thiol reactivity through the α-methylene-γ-lactone group of sesquiterpene lactones. This review will give a brief summary of the anticancer activity of vernolide-A and vernodaline and provide information on the underlying molecular mechanisms.
科研通智能强力驱动
Strongly Powered by AbleSci AI