“野生”型胃肠道间质瘤:分子特征和临床特征的异质性

Yan-hua Mou, Quan Wang, Bin Li
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引用次数: 2

摘要

KIT和血小板衍生生长因子受体α (PDGFRA)被认为是胃肠道间质瘤(gist)中最受驱动的基因。然而,在没有KIT和PDGFRA突变的gist中,约有10%-15%被命名为“野生型”(Wild-type, WT) gist。WT型gist的基因异常和临床特征与KIT/ pdgfr突变的gist有显著差异。近年来,基于下一代测序的发现,WT - gist已被证明不是单一的疾病实体,而是多种病理和临床疾病的集合。然而,尽管在WT - gist中已经发现了一些遗传改变,但这些分子的确切作用尚未得到很好的定义。我们在此总结了KIT/PDGFRA WT gist的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The “Wild”-type gastrointestinal stromal tumors: Heterogeneity on molecule characteristics and clinical features
KIT and platelet-derived growth factor receptor alpha (PDGFRA) are known as the most driven genes in gastrointestinal stromal tumors (GISTs). However, about 10%–15% of GISTs without KIT and PDGFRA mutation are named “Wild-type” (WT) GISTs. Gene abnormalities and clinical features of WT GISTs are significantly different from KIT/PDGFRA-mutated GISTs. Recently, based on the findings of next-generation sequencing, WT GISTs have been shown to be not a single disease entity, but instead a set of various pathologic and clinical diseases. Nevertheless, although several genetic alterations have been identified in WT GISTs, the exact roles of these molecules have not yet been well defined. We herein summarize the recent progression on KIT/PDGFRA WT GISTs.
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