溃疡性结肠炎
疾病
炎症性肠病
活性氧
程序性细胞死亡
肠粘膜
结肠炎
脂质过氧化
癌症研究
细胞
医学
治疗方法
免疫学
氧化应激
生物
细胞凋亡
病理
内科学
细胞生物学
生物化学
遗传学
作者
Jinke Huang,Jiaqi Zhang,Jinxin Ma,Jing Ma,Jiali Liu,Fengyun Wang,Xudong Tang
摘要
Ulcerative colitis (UC) is a recurrent and persistent nonspecific inflammatory bowel disease (IBD) that greatly affects human survival and social wealth. Despite the advances in the treatment of UC, there is still a high demand for novel therapeutic strategies for UC patients. Cell death is critical to the development and progression of UC. Understanding how intestinal cells die and how to prevent damage to intestinal cells is of great interest for the diagnosis and early treatment of UC. Ferroptosis, a novel form of regulated cell death (RCD) manifested by iron accumulation, lipid peroxidation, and excessive reactive oxygen species (ROS) production, has been shown to contribute to the development and progression of UC. Inhibitors of ferroptosis have been validated in models of UC. Here, we reviewed the mechanisms of initiation and control of ferroptosis and summarize the therapeutic activity of ferroptosis inhibitors in models of UC. We further discussed the possibility of inhibiting ferroptosis as a novel therapeutic target for UC. These findings revealed novel mechanisms to protect the colonic mucosa and highlighted the importance of ferroptosis in the disease process.
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