The complexity of the complicity of mast cells in cancer

被引:31
|
作者
Nechushtan, Hovav [1 ]
机构
[1] Hadassah Hebrew Univ, Med Ctr, IL-91120 Jerusalem, Israel
关键词
Mast cells; Cancer; Angiogenesis; c-Kit; Tyrosine kinase inhibitors; IMATINIB MESYLATE; C-KIT; ANGIOGENESIS; INFLAMMATION; CARCINOMA; GROWTH; TUMORS; BETA;
D O I
10.1016/j.biocel.2009.12.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mast cells are evolutionarly ancient cells of the immune cells which can secrete a variety of effector molecules. Animal and pathologic studies suggest that mast cells may promote tumor growth in some cancer types but may act in an opposite manner in others. In several mouse models a critical role of mast cells for tumor promotion was demonstrated. In humans mast cells are dependent upon the tyrosine kinase receptor c-Kit. This receptor is inhibited by many of the new anti-cancer tyrosine kinase inhibitors including Pazopanib, Imatinib and Masitinib. These drugs probably ablate some tumor mast cells, in addition to their other known antitumor effects. Understanding the complex roles of mast cells in cancer should aid in understanding mechanisms of current tyrosine kinase inhibitors, and the development of innovative anti-cancer therapies. Cell facts Mast cells are evolutionarly ancient. Mast cells are dependent on the tyrosine kinase c-Kit. Mast cells produce a wide variety of effector molecules including cytokines. Mast cells are abundant in many cancer types. Mast cells have distinct effects on angiogenesis and immune response. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:551 / 554
页数:4
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