Targeting c-kit in the therapy of mast cell disorders: Current update

被引:31
作者
El-Agamy, Dina S. [1 ]
机构
[1] Mansoura Univ, Fac Pharm, Dept Pharmacol & Toxicol, Mansoura 35516, Egypt
关键词
Mast cells; Tyrosine kinase; C-kit; SCF; TYROSINE KINASE INHIBITORS; IMATINIB MESYLATE; ALLERGIC INFLAMMATION; RHEUMATOID-ARTHRITIS; MURINE MODEL; MASTOCYTOSIS; DISEASES; ASTHMA; GROWTH; PATHOGENESIS;
D O I
10.1016/j.ejphar.2012.06.030
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Classically, mast cells have been widely associated with allergic reactions and parasite infections, but recent studies have elucidated the important role of these cells in innate and acquired immunity, wound healing, fibrosis, and chronic inflammatory diseases. Mast cells release an impressive array of proinflammatory and immunoregulatory mediators after activation induced by either immunoglobulin-E (IgE)-dependent or IgE-independent mechanisms. Proliferation, differentiation, survival and activation of mast cells are regulated by stem cell factor (SCF), the ligand for the c-kit tyrosine kinase receptor which is expressed on the mast cell surface. Inappropriate c-kit activation causes accumulation of mast cells in tissues resulting in mastocytosis. A number of activating mutations in c-kit have recently been identified and these mutations results in aberrant mast cell growth. Thus, c-kit inhibitors may have potential application in multiple conditions associated with mast cell disorders including systemic mastocytosis, anaphylaxis, and asthma. The present perspective aims to summarize recent findings in mast cell biology and the role of c-kit tyrosine kinase inhibitors in the treatment of different mast cell associated disorders. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 3
页数:3
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