STAT1
状态5
斯达
炎症性肠病
JAK-STAT信号通路
疾病
炎症体
医学
药理学
药物发现
信号转导
磺胺吡啶
药品
炎症
免疫学
癌症研究
溃疡性结肠炎
内科学
生物信息学
生物
车站3
受体
干扰素
细胞生物学
酪氨酸激酶
作者
Haowei Cai,Zhuorong Liu,Ping Sun,Yinghua Zhou,Yuyun Yan,Yiming Luo,Xiuxiu Zhang,Ruiwen Wu,Xiangting Liang,Dan Wu,Wenhui Hu,Zhongjin Yang
摘要
Currently, a significant proportion of inflammatory bowel disease (IBD) patients fail to respond to conventional drug therapy such as immunosuppressants and biologic agents. Interference with the JAK/STAT pathway and blocking of IL-1 signaling are two promising therapeutic strategies for these unresponsive IBD patients. This work describes the discovery of an inhibitor 10v that not only blocks NLRP3 and AIM-2 inflammasome-mediated IL-1β signaling, but also reduces the expression of STAT1 and STAT5 in the JAK/STAT pathway. Importantly, 10v exhibits a significant anti-IL-1β effect and decreases the levels of STAT1 and STAT5 in a mouse model of colitis. As a result, a novel small molecule is identified with a dual inhibitory capacity towards both inflammasomes/IL-1β and STAT pathways, which supports further exploration of the therapeutic potential for IBD patients that do not respond to current drug therapy.
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