Clonally resolved single-cell multi-omics identifies routes of cellular differentiation in acute myeloid leukemia

Sergi Beneyto‐Calabuig(Universitat Pompeu Fabra), Anne Kathrin Merbach(Heidelberg University), Jonas-Alexander Kniffka(Heidelberg University), Magdalena Antes(German Cancer Research Center), Chelsea Szu‐Tu(Centre for Genomic Regulation), Christian Rohde(Heidelberg University), Alexander Waclawiczek(German Cancer Research Center), Patrick Stelmach(German Cancer Research Center), Sarah Gräßle(Max Delbrück Center), Philip Pervan(Centre for Genomic Regulation), Maike Janssen(Heidelberg University), Jonathan J. M. Landry(European Molecular Biology Laboratory), Vladimı́r Beneš(European Molecular Biology Laboratory), Anna Jauch(Heidelberg University), Michaela Brough(Heidelberg University), Marcus Bauer(Martin Luther University Halle-Wittenberg), Birgit Besenbeck(Heidelberg University), Julia Felden(Heidelberg University), Sebastian Bäumer(University Hospital Münster), Michael Hundemer(Heidelberg University), Tim Sauer(Heidelberg University), Caroline Pabst(Heidelberg University), Claudia Wickenhauser(Martin Luther University Halle-Wittenberg), Linus Angenendt(University Hospital of Basel), Christoph Schliemann(University Hospital Münster), Andreas Trumpp(German Cancer Research Center), Simon Haas(German Cancer Research Center), Michael Scherer(Centre for Genomic Regulation), Simon Raffel(Heidelberg University), Carsten Müller‐Tidow(European Molecular Biology Organization), Lars Velten(Universitat Pompeu Fabra)
Cell stem cell
April 24, 2023
Cited by 93Open Access
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Abstract

Inter-patient variability and the similarity of healthy and leukemic stem cells (LSCs) have impeded the characterization of LSCs in acute myeloid leukemia (AML) and their differentiation landscape. Here, we introduce CloneTracer, a novel method that adds clonal resolution to single-cell RNA-seq datasets. Applied to samples from 19 AML patients, CloneTracer revealed routes of leukemic differentiation. Although residual healthy and preleukemic cells dominated the dormant stem cell compartment, active LSCs resembled their healthy counterpart and retained erythroid capacity. By contrast, downstream myeloid progenitors constituted a highly aberrant, disease-defining compartment: their gene expression and differentiation state affected both the chemotherapy response and leukemia's ability to differentiate into transcriptomically normal monocytes. Finally, we demonstrated the potential of CloneTracer to identify surface markers misregulated specifically in leukemic cells. Taken together, CloneTracer reveals a differentiation landscape that mimics its healthy counterpart and may determine biology and therapy response in AML.


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