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Single-cell atlas of AML reveals age-related gene regulatory networks in t(8;21) AML.

Jessica Whittle | Stefan Meyer | Georges Lacaud | Syed Murtuza-Baker | Mudassar Iqbal
eLife | 2026

Acute myeloid leukemia (AML) is characterized by cellular and genetic heterogeneity, which correlates with clinical course. Although single-cell RNA sequencing (scRNA-seq) reflects this diversity to some extent, the low sample numbers in individual studies limit the analytic potential when comparing specific patient groups. We performed large-scale integration of published scRNA-seq datasets to create a unique single-cell transcriptomic atlas for AML (AML scAtlas), totaling 748,679 cells, from 159 AML patients and 51 healthy donors from 20 different studies. This is the largest single-cell data resource for human AML to our knowledge, publicly available at https://cellxgene.cziscience.com/collections/071b706a-7ea7-47a4-bddf-6457725839fc. This AML scAtlas allowed investigations into 20 patients with t(8;21) AML, where we explored the clinical importance of age, given the in-utero origin of pediatric disease. We uncovered age-associated gene regulatory network (GRN) signatures, which we validated using bulk RNA sequencing data to delineate distinct groups with divergent biological characteristics. Furthermore, using an additional multiomic dataset (scRNA-seq and scATAC-seq), we validated our initial findings and created a de-noised enhancer-driven GRN reflecting the previously defined age-related signatures. Applying integrated data analysis of the AML scAtlas, we reveal age-dependent gene regulation in t(8;21) AML, potentially reflecting immature/fetal HSC origin in prenatal origin disease vs postnatal origin. Our analysis revealed that BCLAF1, which is particularly enriched in pediatric AML with t(8;21) of inferred in-utero origin, is a promising prognostic indicator. The AML scAtlas provides a powerful resource to investigate molecular mechanisms underlying different AML subtypes.

Pubmed ID: 41671045

Research resources used in this publication

None found

Antibodies used in this publication

None found

Associated grants

  • Agency: Medical Research Council, United Kingdom
    Id: MR/W007428/1
  • Agency: Blood Cancer UK, United Kingdom
    Id: 15038
  • Agency: Children's Cancer and Leukaemia Group,
    Id: 2016 09
  • Agency: Cancer Research UK, United Kingdom
    Id: C5759/A20971
  • Agency: Cancer Research UK, United Kingdom
    Id: C5759/A27412
  • Agency: Blood Cancer UK, United Kingdom
    Id: 23002
  • Agency: Medical Research Council, United Kingdom
    Id: MR/X014088/1

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