Department of Pediatrics, Oncology and Hematology, Medical University of Lodz, Lodz, Poland.
Postgraduate School of Molecular Medicine, Medical University of Warsaw, Warsaw, Poland.
Genes Chromosomes Cancer. 2019 Sep;58(9):619-626. doi: 10.1002/gcc.22748. Epub 2019 Apr 3.
The germline variant at rs3824662 in GATA3 is a risk locus for Philadelphia-like acute lymphoblastic leukemia (Ph-like ALL), the biological subtype of B-cell precursor (BCP)-ALL defined by a distinct gene expression profile and the presence of specific somatic aberrations including rearrangements of CRLF2. In this study, we investigated whether rs3824662 in GATA3 associates with CRLF2 expression in leukemic cells and predicts prognosis in pediatric BCP-ALL patients treated according to the ALL Intercontinental Berlin-Frankfurt-Münster (IC BFM) 2009 (n = 645) and the ALL IC BFM 2002 (n = 216) protocols. High expression of CRLF2 was observed at both protein and mRNA levels (fourfold higher in AA than in CA + CC) among GATA3 AA variant carriers, independent of the presence of P2RY8-CRLF2 fusion. Additionally, the AA variant at rs3824662 was a significant factor affecting minimal residual disease level at the end of induction phase and overall survival regardless of the risk group and the protocol. The germline variant at rs3824662 in GATA3 is a prognostic factor which associates with CRLF2 expression in leukemic cells supporting the hypothesis that GATA3 may have a regulatory effect on the CRLF2 pathway in pediatric BCP-ALL.
GATA3 基因座上的 rs3824662 种系变异是费城样急性淋巴细胞白血病(Ph-like ALL)的风险位点,Ph-like ALL 是 B 细胞前体(BCP)-ALL 的生物学亚型,其定义为独特的基因表达谱和特定体细胞异常的存在,包括 CRLF2 的重排。在这项研究中,我们调查了 GATA3 基因座上的 rs3824662 是否与白血病细胞中的 CRLF2 表达相关,并预测了根据 ALL 国际柏林-法兰克福-慕尼黑(IC BFM)2009(n=645)和 ALL IC BFM 2002(n=216)方案治疗的儿科 BCP-ALL 患者的预后。在 GATA3 AA 变异携带者中,无论是存在 P2RY8-CRLF2 融合与否,CRLF2 的蛋白和 mRNA 水平均表现出高表达(AA 是 CA+CC 的四倍)。此外,rs3824662 上的 AA 变异是一个显著的影响因素,与风险组和方案无关,它影响诱导期结束时微小残留病水平和总生存率。GATA3 基因座上的 rs3824662 种系变异是一个预后因素,它与白血病细胞中的 CRLF2 表达相关,这支持了 GATA3 可能对儿科 BCP-ALL 中的 CRLF2 通路具有调节作用的假说。