MRC2 expression modulates metabolism in acute myeloid leukemia stem cells

Leukemic stem cells (LSC) are well recognized for their essential roles in acute myeloid leukemia (AML) initiation and relapse. LSC can be distinguished from non-LSC AML cells by the expression of specific cell surface markers, but there is considerable phenotypic heterogeneity among LSC in AML. Here, using primary patient samples, we report that mannose receptor C-type 2 (MRC2) can be used to enrich for LSC across various AML subtypes. When compared to MRC2- AML cells isolated from the same patient samples, MRC2+ leukemic subpopulations show increased in vitro clonogenic capacity, a stemness transcriptomic signature, and enhanced leukemic capacity in mouse xenograft models. Further, we find that MRC2 is functional on AML cells, and enables their robust uptake of collagen, which supports their glycolytic metabolism. In sum these data highlight the use of functional surface markers to distinguish LSC in AML, and how they can yield insight into their unique characteristics.

Authors

Institutions

Publication Details

Journal
Cancer Letters
Published
2025-09-27
DOI
https://doi.org/10.1016/j.canlet.2025.218068
Primary Topic
Biochemical and Molecular Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

MRC2 expression modulates metabolism in acute myeloid leukemia stem cells

Taylor Mills, A. Stanger, Saskia Rudat, Lucas Mix et al.
Cancer Letters
Biochemical and Molecular Research
article

MRC2 expression modulates metabolism in acute myeloid leukemia stem cells

Taylor Mills, A. Stanger, Saskia Rudat, Lucas Mix, Florian Büttner, Elsa Görsch, Matthias Schwab, Jan C. Schroeder, Jan Frederic Weller, Simone Poeschel, Marlon Arnone, Claudia Lengerke, Stefan Winter, Jessica Kuebler, Lucca M. Kimmich
article en

Abstract

Leukemic stem cells (LSC) are well recognized for their essential roles in acute myeloid leukemia (AML) initiation and relapse. LSC can be distinguished from non-LSC AML cells by the expression of specific cell surface markers, but there is considerable phenotypic heterogeneity among LSC in AML. Here, using primary patient samples, we report that mannose receptor C-type 2 (MRC2) can be used to enrich for LSC across various AML subtypes. When compared to MRC2- AML cells isolated from the same patient samples, MRC2+ leukemic subpopulations show increased in vitro clonogenic capacity, a stemness transcriptomic signature, and enhanced leukemic capacity in mouse xenograft models. Further, we find that MRC2 is functional on AML cells, and enables their robust uptake of collagen, which supports their glycolytic metabolism. In sum these data highlight the use of functional surface markers to distinguish LSC in AML, and how they can yield insight into their unique characteristics.

Cancer LettersVol. 635
Universität Hamburg (DE), University Medical Center Hamburg-Eppendorf (DE), Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology (DE), STZ eyetrial (DE), University of Tübingen (DE)
Openalex Percentile: Top 76%
Biochemical and Molecular Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.