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KIT基因第11外显子缺失-倒位代表胃肠道间质瘤中的复杂突变。

KIT exon 11 deletion-inversions represent complex mutations in gastrointestinal stromal tumors.

作者信息

Lasota Jerzy, Miettinen Markku

机构信息

Department of Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000, USA.

出版信息

Cancer Genet Cytogenet. 2007 May;175(1):69-72. doi: 10.1016/j.cancergencyto.2006.12.010.

Abstract

Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the gastrointestinal tract. KIT expression and mutational KIT activation have been documented in a majority of GISTs. Most mutations have been found in KIT juxtamembrane domain encoded by exon 11. Recently, we have identified three, complex KIT exon 11 mutations previously unreported in GISTs. These mutations consisted of several nucleotide deletions accompanied by insertions of inverted complementary DNA strand sequences. All three mutations were found in the 5' part of KIT exon 11. At the protein level, these mutations lead to the same end result: in-frame loss and insertion of a number of amino acids and could be considered examples of deletion-insertion. Although proper description of these mutations at the genomic level is a complex task and requires an individual approach, the uniform name deletion-inversion is suggested for this type of mutation, based on the present study. The frequency of deletion-inversions among KIT exon 11 mutant GISTs was estimated to be <0.5%, based on evaluation of 700 KIT exon 11 mutants. Molecular events leading to formation of deletion-inversions remain elusive and should be studied further.

摘要

胃肠道间质瘤(GISTs)是胃肠道最常见的间叶组织肿瘤。大多数GISTs中已证实存在KIT表达及KIT激活突变。多数突变见于第11外显子编码的KIT近膜结构域。最近,我们鉴定出3种GISTs中此前未报道的复杂的KIT第11外显子突变。这些突变包括几个核苷酸缺失并伴有反向互补DNA链序列插入。所有3种突变均见于KIT第11外显子的5′端。在蛋白质水平,这些突变导致相同的最终结果:框内若干氨基酸缺失和插入,可视为缺失-插入的实例。尽管在基因组水平对这些突变进行恰当描述是一项复杂任务且需要个体化方法,但基于本研究,建议将此类突变统一命名为缺失-倒位。根据对700个KIT第11外显子突变体的评估,KIT第11外显子突变的GISTs中缺失-倒位的频率估计<0.5%。导致缺失-倒位形成的分子事件仍不清楚,应进一步研究。

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