Walz Christoph, Curtis Claire, Schnittger Susanne, Schultheis Beate, Metzgeroth Georgia, Schoch Claudia, Lengfelder Eva, Erben Philipp, Müller Martin C, Haferlach Torsten, Hochhaus Andreas, Hehlmann Rüdiger, Cross Nicholas C P, Reiter Andreas
III. Medizinische Universitätsklinik, Fakultät für Klinische Medizin Mannheim der Universität Heidelberg, Mannheim, Germany.
Genes Chromosomes Cancer. 2006 Oct;45(10):950-6. doi: 10.1002/gcc.20359.
Chronic myeloproliferative disorders with rearrangements of the platelet-derived growth factor receptor A (PDGFRA) gene at chromosome band 4q12 have shown excellent responses to targeted therapy with imatinib. Here we report a female patient who presented with advanced phase of a chronic eosinophilic leukemia. Cytogenetic analysis revealed an ins(9;4)(q33;q12q25) in 5 of 21 metaphases. FISH analysis with flanking BAC probes indicated that PDGFRA was disrupted. A novel mRNA in-frame fusion between exon 13 of the CDK5 regulatory subunit associated protein 2 (CDK5RAP2) gene, a 40-bp insert that was partially derived from an inverted sequence stretch of PDGFRA intron 9, and a truncated PDGFRA exon 12 was identified by 5'-RACE-PCR. CDK5RAP2 encodes a protein that is believed to be involved in centrosomal regulation. The predicted CDK5RAP2-PDGFRA protein consists of 1,003 amino acids and retains both tyrosine kinase domains of PDGFRA and several potential dimerization domains of CDK5RAP2. Despite achieving complete cytogenetic and molecular remission on imatinib, the patient relapsed with imatinib-resistant acute myeloid leukemia that was characterized by a normal karyotype, absence of detectable CDK5RAP2-PDGFRA mRNA, and a newly acquired G12D NRAS mutation.
血小板衍生生长因子受体A(PDGFRA)基因在染色体4q12带发生重排的慢性骨髓增殖性疾病对伊马替尼靶向治疗显示出良好反应。在此,我们报告一名患有晚期慢性嗜酸性粒细胞白血病的女性患者。细胞遗传学分析显示,在21个中期细胞中有5个存在ins(9;4)(q33;q12q25)。用侧翼BAC探针进行FISH分析表明PDGFRA被破坏。通过5'-RACE-PCR鉴定出一种新的mRNA框内融合,其发生在细胞周期蛋白依赖性激酶5调节亚基相关蛋白2(CDK5RAP2)基因的第13外显子、一个部分源自PDGFRA内含子9反向序列延伸的40bp插入片段与截短的PDGFRA第12外显子之间。CDK5RAP2编码一种据信参与中心体调节的蛋白质。预测的CDK5RAP2-PDGFRA蛋白由1003个氨基酸组成,保留了PDGFRA的两个酪氨酸激酶结构域以及CDK5RAP2的几个潜在二聚化结构域。尽管该患者在伊马替尼治疗下实现了完全细胞遗传学和分子缓解,但仍复发为伊马替尼耐药的急性髓系白血病,其特征为核型正常、未检测到CDK5RAP2-PDGFRA mRNA以及新获得的G12D NRAS突变。