PDGFRA公司
骨髓增生性肿瘤
融合基因
外显子
癌症研究
断点
生物
基因
遗传学
染色体
免疫学
间质细胞
骨髓纤维化
骨髓
主旨
作者
Yuka Sugimoto,Akiko Sada,Yuji Shimokariya,Fumihiko Monma,Kohshi Ohishi,Masahiro Masuya,Tsutomu Nobori,Toshimitsu Matsui,Naoyuki Katayama
出处
期刊:Cancer genetics
[Elsevier]
日期:2015-10-01
卷期号:208 (10): 508-512
被引量:11
标识
DOI:10.1016/j.cancergen.2015.07.001
摘要
We identified a novel fusion gene, FOXP1-PDGFRA, in a patient with myeloproliferative neoplasm (MPN) with eosinophilia, harboring the chromosome abnormality t(3;4)(p13;q12). The patient responded well to imatinib and has remained in molecular remission for 3 years. This is the seventh fusion gene involving PDGFRA in MPN with eosinophilia. PDGFRA was truncated in its autoinhibitory domain, as in other PDGFRA-related MPNs, and was fused to FOXP1 at its functional forkhead domain. Comparing genomic DNA with mRNA sequences provides the possibility that the splicing process near the breakpoint junction in the FOXP1-PDGFRA fusion gene may use the normal splice donor site for intron 23a of FOXP1 and the cryptic splice acceptor site in exon 12 of PDGFRA. This is the first report to describe the FOXP1-PDGFRA fusion gene in MPN.
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