MAPK/ERK通路
p38丝裂原活化蛋白激酶
尼古丁
血管生成
癌症研究
癌细胞
NF-κB
细胞因子
化学
癌症
信号转导
生物
细胞生物学
分子生物学
免疫学
遗传学
神经科学
作者
Sen Lian,Shinan Li,Jun Zhu,Yong Xia,Young Do Jung
出处
期刊:Toxicology
[Elsevier BV]
日期:2021-12-08
卷期号:466: 153062-153062
被引量:39
标识
DOI:10.1016/j.tox.2021.153062
摘要
Nicotine, a major alkaloid found in tobacco, is a significant risk factor for gastric cancer. IL-8, a pleiotropic cytokine, plays a vital role in cancer cell metastasis. The role of nicotine in IL-8 expression and the underlying mechanism is currently unknown. Here, we examined the effects of nicotine on IL-8 expression and explored the potential mechanisms in gastric cancer cells. We found that nicotine increases IL-8 expression. Specific inhibitor and mutagenesis studies showed that ROS and MAPK (Erk1/2, p38) were involved in this process. Deletion and site-directed mutagenesis studies indicate the involvement of transcription factor NF-κB and AP-1. ROS and ROS/MAPK (Erk1/2, p38) functioned as the upstream signaling molecules in the activation of NF-κB and AP-1, respectively. AGS gastric cancer cells pretreated with nicotine stimulate angiogenesis in the tumor microenvironment, partially abrogated by silencing IL-8 in AGS cells. In this study, we found that nicotine induces IL-8 expression via ROS/NF-κB and ROS/MAPK (Erk1/2, p38)/AP-1 axis in gastric cancer cells, thus stimulating endothelial cell proliferation and angiogenesis in the tumor microenvironment.
科研通智能强力驱动
Strongly Powered by AbleSci AI