PDGFRA公司
主旨
克拉斯
癌症研究
神经母细胞瘤RAS病毒癌基因同源物
原癌基因蛋白质c-kit
外显子
突变
生物
间质细胞
PI3K/AKT/mTOR通路
医学
基因
信号转导
遗传学
造血
干细胞
干细胞因子
作者
Marc Daniels,Irene Lurkin,R. Pauli,E Erbstösser,Uwe Hildebrandt,Karsten Hellwig,Uwe Zschille,Petra Lüders,Gabriele Krüger,J. Knolle,Bernd Stengel,Friedrich Prall,K. Hertel,H. Lobeck,Brigitte Popp,F Theissig,Peter H. Wünsch,Ellen C. Zwarthoff,Abbas Agaimy,Regine Schneider‐Stock
出处
期刊:Cancer Letters
[Elsevier]
日期:2011-12-01
卷期号:312 (1): 43-54
被引量:126
标识
DOI:10.1016/j.canlet.2011.07.029
摘要
Pathogenetic pathways of gastrointestinal stromal tumors (GIST) lacking mutations in KIT and PDGFRA (∼15%) are still poorly studied. Nearly nothing is known about PI3K alterations in GISTs and only a few GISTs with BRAF mutations have been reported. BRAF mutations (V600E) were found in 3/87 tumors (3.5%) concomitantly were wild type for KIT and PDGFRA. No mutations were detected in KRAS, NRAS, and FGFR3. For the first-time we demonstrated a PIK3CA mutation (H1047L) simultaneously occurring with a 15-bp deletion in KIT exon 11 in one tumor. We suggest that BRAF mutations are of pathogenetic significance in wild type GISTs. The PI3K pathway should be assessed in future studies.
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