LLR Molecular Haematology Unit, NDCLS, RDM, John Radcliffe Hospital, Oxford, UK.
Br J Haematol. 2013 Oct;163(2):235-9. doi: 10.1111/bjh.12491. Epub 2013 Jul 24.
Whole exome sequencing was performed in a patient with myelodysplastic syndrome before and after progression to acute myeloid leukaemia. Mutations in several genes, including SETBP1, were identified following leukaemic transformation. Screening of 328 patients with myeloid disorders revealed SETBP1 mutations in 14 patients (4·3%), 7 of whom had -7/del(7q) and 3 had i(17)(q10), cytogenetic markers associated with shortened overall survival and increased risk of leukaemic evolution. SETBP1 mutations were frequently acquired at the time of leukaemic evolution, coinciding with increase of leukaemic blasts. These data suggest that SETBP1 mutations may play a role in MDS and chronic myelomonocytic leukaemia disease progression.
在一位从骨髓增生异常综合征进展为急性髓系白血病的患者中,我们进行了全外显子组测序。白血病转化后,发现了包括 SETBP1 在内的几个基因突变。对 328 例骨髓疾病患者的筛查发现,有 14 例(4.3%)患者存在 SETBP1 突变,其中 7 例存在 -7/del(7q),3 例存在 i(17)(q10),这些细胞遗传学标志物与总生存期缩短和白血病演变风险增加相关。SETBP1 突变通常在白血病演变时获得,与白血病母细胞的增加相吻合。这些数据表明,SETBP1 突变可能在 MDS 和慢性粒单核细胞白血病的疾病进展中发挥作用。