Classes of c-KIT activating mutations:: proposed mechanisms of action and implications for disease classification and therapy

被引:260
作者
Longley, BJ
Reguera, MJ
Ma, YS
机构
[1] Columbia Univ, Dept Dermatol, New York, NY 10031 USA
[2] Columbia Univ, Dept Pathol, New York, NY 10031 USA
[3] Univ Autonoma Barcelona, Fac Vet, Dept Histol & Pathol, E-08193 Barcelona, Spain
基金
美国国家卫生研究院;
关键词
c-KIT; mastocytosis; GIST; AML; gastrointestinal stromal tumors; acute myelogenous leukemia; sinonasal T-cell lymphoma; myelodysplasia;
D O I
10.1016/S0145-2126(01)00028-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mutations causing constitutive activation of KIT have been shown to be causative in some forms of mastocytosis, and several types of mutations have been associated with myeloproliferative disorders (MPDs), acute myelogenous leukemia (AML), sinonasal lymphomas, and gastrointestinal stromal tumors (GIST). We divide these activating mutation into two types - 'regulatory type' mutations, which affect regulation of the kinase molecule, and 'enzymatic pocket type' mutations, which alter the amino acid sequence directly forming the enzymatic site. KIT inhibitors have been suggested as therapeutic drugs for these conditions, but different types of activating mutations respond differentially to KIT inhibitors, so classification of individuals on the basis of specific mutations is necessary to guide therapy. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:571 / 576
页数:6
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