Department of Pharmacy and Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN.
Center for Applied Bioinformatics, St. Jude Children's Research Hospital, Memphis, TN.
Blood. 2023 Jul 13;142(2):172-184. doi: 10.1182/blood.2023019765.
Trisomy 21, the genetic cause of Down syndrome (DS), is the most common congenital chromosomal anomaly. It is associated with a 20-fold increased risk of acute lymphoblastic leukemia (ALL) during childhood and results in distinctive leukemia biology. To comprehensively define the genomic landscape of DS-ALL, we performed whole-genome sequencing and whole-transcriptome sequencing (RNA-Seq) on 295 cases. Our integrated genomic analyses identified 15 molecular subtypes of DS-ALL, with marked enrichment of CRLF2-r, IGH::IGF2BP1, and C/EBP altered (C/EBPalt) subtypes compared with 2257 non-DS-ALL cases. We observed abnormal activation of the CEBPD, CEBPA, and CEBPE genes in 10.5% of DS-ALL cases via a variety of genomic mechanisms, including chromosomal rearrangements and noncoding mutations leading to enhancer hijacking. A total of 42.3% of C/EBP-activated DS-ALL also have concomitant FLT3 point mutations or insertions/deletions, compared with 4.1% in other subtypes. CEBPD overexpression enhanced the differentiation of mouse hematopoietic progenitor cells into pro-B cells in vitro, particularly in a DS genetic background. Notably, recombination-activating gene-mediated somatic genomic abnormalities were common in DS-ALL, accounting for a median of 27.5% of structural alterations, compared with 7.7% in non-DS-ALL. Unsupervised hierarchical clustering analyses of CRLF2-rearranged DS-ALL identified substantial heterogeneity within this group, with the BCR::ABL1-like subset linked to an inferior event-free survival, even after adjusting for known clinical risk factors. These results provide important insights into the biology of DS-ALL and point to opportunities for targeted therapy and treatment individualization.
21 三体,唐氏综合征(DS)的遗传原因,是最常见的先天性染色体异常。它与儿童时期 20 倍的急性淋巴细胞白血病(ALL)风险增加相关,并导致独特的白血病生物学。为了全面定义 DS-ALL 的基因组景观,我们对 295 例病例进行了全基因组测序和全转录组测序(RNA-Seq)。我们的综合基因组分析确定了 15 种 DS-ALL 的分子亚型,与 2257 例非 DS-ALL 病例相比,CRLF2-r、IGH::IGF2BP1 和 C/EBP 改变(C/EBPalt)亚型明显富集。我们通过多种基因组机制,包括染色体重排和导致增强子劫持的非编码突变,观察到 10.5%的 DS-ALL 病例中 CEBPD、CEBPA 和 CEBPE 基因异常激活。共有 42.3%的 C/EBP 激活的 DS-ALL 还伴有同时的 FLT3 点突变或插入/缺失,而在其他亚型中这一比例为 4.1%。CEBPD 过表达增强了体外造血祖细胞向前 B 细胞的分化,尤其是在 DS 遗传背景下。值得注意的是,重组激活基因介导的体细胞基因组异常在 DS-ALL 中很常见,占结构改变的中位数为 27.5%,而非 DS-ALL 中为 7.7%。CRLF2 重排的 DS-ALL 的无监督层次聚类分析在该组内发现了实质性的异质性,BCR::ABL1 样亚组与无事件生存相关,即使在调整了已知的临床危险因素后也是如此。这些结果为 DS-ALL 的生物学提供了重要的见解,并为靶向治疗和个体化治疗指明了方向。