Goel Anita, Prasad Ashok K, Parmar Virinder S, Ghosh Balaram, Saini Neeru
Molecular Immunogenetics Laboratory, Institute of Genomics and Integrative Biology, Mall Road, Delhi 110 007, India.
FEBS Lett. 2007 May 29;581(13):2447-54. doi: 10.1016/j.febslet.2007.04.052. Epub 2007 Apr 30.
Coumarins have attracted intense interest in recent years because they have been identified from natural sources, especially green plants and have diverse pharmacological properties. In this study, we investigated whether 7,8-dihydroxy-4-methylcoumarin (DHMC) caused apoptosis in A549 human non-small cell lung carcinoma cells (NSCLC) and, if so, by what mechanisms. Here, we show that, in A549 human NSCLC cells, DHMC induces apoptosis through mitochondria-mediated caspase-dependent pathway. Although an increase in the levels of reactive oxygen species (ROS) was observed, pre-treatment with antioxidant showed no protective effect against DHMC-induced apoptosis. In addition, our immunoblot data revealed that DHMC treatment led to down-regulation of Bcl-xl, Bax, p21, Cox-2, p53 and upregulation of c-Myc. Results in the present study for the first time suggest that DHMC induces apoptosis in human lung A549 cells through partial inhibition of ERK/MAPK signaling.
近年来,香豆素因其来源于天然物质,尤其是绿色植物,且具有多种药理特性而备受关注。在本研究中,我们探究了7,8-二羟基-4-甲基香豆素(DHMC)是否会导致A549人非小细胞肺癌细胞(NSCLC)凋亡,若会导致凋亡,则其作用机制是什么。在此,我们表明,在A549人NSCLC细胞中,DHMC通过线粒体介导的半胱天冬酶依赖性途径诱导细胞凋亡。尽管观察到活性氧(ROS)水平升高,但用抗氧化剂预处理对DHMC诱导的细胞凋亡没有保护作用。此外,我们的免疫印迹数据显示,DHMC处理导致Bcl-xl、Bax、p21、Cox-2、p53下调,c-Myc上调。本研究结果首次表明,DHMC通过部分抑制ERK/MAPK信号传导诱导人肺A549细胞凋亡。