Targeting Macrophage Migration Inhibitory Factor in Acute Pancreatitis and Pancreatic Cancer

被引:27
作者
Wen, Yongjian [1 ,2 ,3 ,4 ]
Cai, Wenhao [1 ,2 ,5 ,6 ]
Yang, Jingyu [1 ,2 ]
Fu, Xianghui [7 ,8 ]
Putha, Lohitha [9 ]
Xia, Qing [1 ,2 ]
Windsor, John A. [3 ]
Phillips, Anthony R. [3 ,4 ]
Tyndall, Joel D. A. [9 ]
Du, Dan [10 ]
Liu, Tingting [1 ,2 ]
Huang, Wei [1 ,2 ,5 ,6 ]
机构
[1] Sichuan Univ, West China Hosp, Sichuan Prov Pancreatitis Ctr, Dept Integrated Tradit Chinese & Western Med, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp, West China Liverpool Biomed Res Ctr, Chengdu, Peoples R China
[3] Univ Auckland, Fac Med & Hlth Sci, Surg & Translat Res Ctr, Auckland, New Zealand
[4] Univ Auckland, Sch Biol Sci, Appl Surg & Metab Lab, Auckland, New Zealand
[5] Univ Liverpool, Liverpool Univ Hosp NHS Fdn Trust, Liverpool Pancreatitis Res Grp, Liverpool, Merseyside, England
[6] Univ Liverpool, Inst Syst Mol & Integrat Biol, Liverpool, Merseyside, England
[7] Sichuan Univ, West China Hosp, Div Endocrinol & Metab, State Key Lab Biotherapy, Chengdu, Peoples R China
[8] Collaborat Innovat Ctr Biotherapy, Chengdu, Peoples R China
[9] Univ Otago, Sch Pharm, Dunedin, New Zealand
[10] Sichuan Univ, West China Hosp, West China Washington Mitochondria & Metab Ctr, Chengdu, Peoples R China
基金
美国国家科学基金会;
关键词
macrophage migration inhibitory factor; acute inflammatory response; toll-like receptor; inflammasome; acute pancreatitis; pancreatic cancer; D-DOPACHROME TAUTOMERASE; FACTOR MIF; CRYSTAL-STRUCTURE; LUNG INJURY; NLRP3; INFLAMMASOME; INSULIN-SECRETION; REGULATORY ROLE; CELL-SURVIVAL; MURINE MODEL; RAT MODEL;
D O I
10.3389/fphar.2021.638950
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Macrophage migration inhibitory factor (MIF) is a pleiotropic cytokine implicated in the pathogenesis of inflammation and cancer. It is produced by various cells and circulating MIF has been identified as a biomarker for a range of diseases. Extracellular MIF mainly binds to the cluster of differentiation 74 (CD74)/CD44 to activate downstream signaling pathways. These in turn activate immune responses, enhance inflammation and can promote cancer cell proliferation and invasion. Extracellular MIF also binds to the C-X-C chemokine receptors cooperating with or without CD74 to activate chemokine response. Intracellular MIF is involved in Toll-like receptor and inflammasome-mediated inflammatory response. Pharmacological inhibition of MIF has been shown to hold great promise in treating inflammatory diseases and cancer, including small molecule MIF inhibitors targeting the tautomerase active site of MIF and antibodies that neutralize MIF. In the current review, we discuss the role of MIF signaling pathways in inflammation and cancer and summarize the recent advances of the role of MIF in experimental and clinical exocrine pancreatic diseases. We expect to provide insights into clinical translation of MIF antagonism as a strategy for treating acute pancreatitis and pancreatic cancer.
引用
收藏
页数:16
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