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Hypoxia inducible factor prolyl hydroxylases in inflammatory bowel disease

Affiliation
Department of Oncology ,Cancer Institute ,The Affiliated Hospital of Qingdao University ,Qingdao ,China
Lun, Jie;
Affiliation
Shandong Provincial Maternal and Child Health Care Hospital Affiliated to Qingdao University ,Jinan ,China
Zhang, Hongwei;
Affiliation
Department of Oncology ,Cancer Institute ,The Affiliated Hospital of Qingdao University ,Qingdao ,China
Guo, Jing;
Affiliation
Department of Gastroenterology ,Qingdao Municipal Hospital ,Qingdao ,China
Yu, Mengchao;
Affiliation
Department of Oncology ,Cancer Institute ,The Affiliated Hospital of Qingdao University ,Qingdao ,China
Fang, Jing

Inflammatory bowel disease (IBD) is a chronic disease that is characterized by intestinal inflammation. Epithelial damage and loss of intestinal barrier function are believed to be the hallmark pathologies of the disease. In IBD, the resident and infiltrating immune cells consume much oxygen, rendering the inflamed intestinal mucosa hypoxic. In hypoxia, the hypoxia-inducible factor (HIF) is induced to cope with the lack of oxygen and protect intestinal barrier. Protein stability of HIF is tightly controlled by prolyl hydroxylases (PHDs). Stabilization of HIF through inhibition of PHDs is appearing as a new strategy of IBD treatment. Studies have shown that PHD-targeting is beneficial to the treatment of IBD. In this Review, we summarize the current understanding of the role of HIF and PHDs in IBD and discuss the therapeutic potential of targeting PHD-HIF pathway for IBD treatment.

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License Holder: Copyright © 2023 Lun, Zhang, Guo, Yu and Fang.

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