Suppr超能文献

RUNX1突变家系中的复发性体细胞JAK-STAT通路变异

Recurrent somatic JAK-STAT pathway variants within a RUNX1-mutated pedigree.

作者信息

Tawana Kiran, Wang Jun, Király Péter A, Kállay Krisztián, Benyó Gábor, Zombori Marianna, Csomor Judit, Al Seraihi Ahad, Rio-Machin Ana, Matolcsy András, Chelala Claude, Cavenagh Jamie, Fitzgibbon Jude, Bödör Csaba

机构信息

Centre for Haemato-Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK.

Bioinformatics Unit, Barts Cancer Institute, Queen Mary University of London, London, UK.

出版信息

Eur J Hum Genet. 2017 Aug;25(8):1020-1024. doi: 10.1038/ejhg.2017.80. Epub 2017 May 17.

Abstract

Germline variants within the transcription factor RUNX1 are associated with familial platelet disorder and acute leukemia in over 40% of carriers. At present, the somatic events triggering leukemic transformation appear heterogeneous and profiles of leukemia initiation across family members are poorly defined. We report a new RUNX1 family where three sisters harboring a germline nonsense RUNX1 variant, c.601C>T (p.(Arg201*)), developed acute myelomonocytic leukemia (AML) at 5 years of age. Whole-exome sequencing of tumor samples revealed all three siblings independently acquired variants within the JAK-STAT pathway, specifically targeting JAK2 and SH2B3 (a negative regulator of JAK2), while also sharing the 46/1 haplotype linked with sporadic JAK2-positive myeloproliferative neoplasms. In-depth chromosomal characterization of tumors revealed acquired copy number gains and uniparental disomy amplifying RUNX1, JAK2 and SH2B3 variants, highlighting the significance of co-operation between these disrupted pathways. One sibling, presenting with myelodysplasia at 14 years, had no evidence of clonal or subclonal JAK2 or SH2B3 variants, suggesting the latter were specifically associated with leukemic transformation in her sisters. Collectively, the clinical and molecular homogeneity across these three young siblings provides the first notable example of convergent AML evolution in a RUNX1 pedigree, with the recurrent acquisition of JAK-STAT pathway variants giving rise to high-risk AML, characterized by chemotherapy resistance and relapse.

摘要

转录因子RUNX1内的种系变异与超过40%的携带者的家族性血小板疾病和急性白血病相关。目前,触发白血病转化的体细胞事件似乎具有异质性,并且家庭成员之间白血病起始的特征尚不明确。我们报告了一个新的RUNX1家族,其中三名姐妹携带种系无义RUNX1变异c.601C>T(p.(Arg201*)),在5岁时患上了急性粒单核细胞白血病(AML)。肿瘤样本的全外显子组测序显示,所有三名兄弟姐妹均在JAK-STAT通路内独立获得了变异,具体靶向JAK2和SH2B3(JAK2的负调节因子),同时还共享与散发性JAK2阳性骨髓增殖性肿瘤相关的46/1单倍型。对肿瘤的深入染色体特征分析显示,获得性拷贝数增加和单亲二倍体扩增了RUNX1、JAK2和SH2B3变异,突出了这些失调通路之间合作的重要性。一名14岁时出现骨髓发育异常的兄弟姐妹没有克隆性或亚克隆性JAK2或SH2B3变异的证据,这表明后者与她姐妹的白血病转化特别相关。总体而言,这三名年轻兄弟姐妹的临床和分子同质性为RUNX1家系中AML趋同进化提供了首个显著例子,JAK-STAT通路变异的反复获得导致了以化疗耐药和复发为特征的高危AML。

相似文献

引用本文的文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验