期刊
ONCOTARGET
卷 7, 期 32, 页码 52218-52229出版社
IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.10582
关键词
melanoma; TRAIL; icariside II; pSTAT3; ROS
资金
- Research Grants Council of Hong Kong [HKBU 262512]
- Food and Health Bureau of Hong Kong [HMRF11122521]
- Science, Technology and Innovation Commission of Shenzhen [JCYJ20140807091945050]
- Hong Kong Baptist University [FRG1/15-16/050, FRG2/15-16/020]
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is a promising antitumor agent. However, many melanoma cells show weak responses to TRAIL. Here, we investigated whether Icariside II (IS), an active component of Herba Epimedii, could potentiate antitumor effects of TRAIL in melanoma cells. Melanoma cells were treated with IS and/or TRAIL and cell death, apoptosis and signal transduction were analyzed. We showed that IS promoted TRAIL-induced cell death and apoptosis in A375 melanoma cells. Mechanistically, IS reduced the expression levels of cFLIP in a phospho-STAT3 (pSTAT3)-dependent manner. Ectopic expression of STAT3 abolished IS-induced cFLIP down-regulation and the associated potentiation of TRAIL-mediated cell death. Moreover, IS-induced reactive oxygen species (ROS) production preceded down-regulation of pSTAT3/cFLIP via activating AKT, and the consequent sensitization of cells to TRAIL. We also found that IS treatment downregulated cFLIP via ROS-mediated NF-lambda B pathway. In addition, IS converted TRAIL-resistant melanoma MeWo and SK-MEL-28 cells into TRAIL-sensitive cells. Taken together, our results indicated that IS potentiated TRAIL-induced apoptosis through ROS-mediated down-regulation of STAT3/cFLIP signaling.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据