Kit and c-kit mutations in mastocytosis:: A short overview with special reference to novel molecular and diagnostic concepts
Kit and c-kit mutations in mastocytosis:: A short overview with special reference to novel molecular and diagnostic concepts
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DOI:
10.1159/000048179
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发表时间:
2002-02-01
影响因子:
2.8
通讯作者:
Arock, M
中科院分区:
文献类型:
--
作者:
Féger, F;Dumas, AR;Arock, M
Mastocytosis is a heterogeneous group of hematopoietic disorders characterized by abnormal growth and accumulation of mast cells (MC) in one or more organs. Clinical symptoms occur as a result of the release of chemical mediators and/or of pathologic infiltration of MC in various tissues. Although the initial events leading to mastocytosis have not yet been unraveled, acquired alterations in the c-kitgene coding for the receptor of stem cell factor (SCF), a major cytokine involved in MC growth, have been described in a significant number of patients. Of particular interest are point mutations resulting in a constitutively activated SCF receptor. Such mutations are probably involved in the abnormal (SCF-independent) proliferation of MC in these patients. New therapeutic strategies may be envisaged to inhibit the deregulated kinase activity of these mutant forms of c-kit. Copyright (C) 2002 S. KargerAG, Basel.