Resolving leukemic stem cell heterogeneity and plasticity with single-cell multiomics
Frank Y Huang1, Andreas Trumpp2, Patrick Stelmach2
1Division of Stem Cells and Cancer, German Cancer Research Center (DKFZ) and DKFZ-ZMBH Alliance, Heidelberg, Germany; Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM, gGmbH), Heidelberg, Germany; Faculty of Biosciences, Heidelberg University, Heidelberg, Germany.
Leukemic stem cells (LSCs) drive acute myeloid leukemia (AML) relapse and are highly diverse. Single-cell multiomics helps understand LSC heterogeneity for better AML diagnostics and treatments.
Area of Science:
- Hematology
- Cancer Biology
- Genomics
Background:
- Acute myeloid leukemia (AML) is driven by diverse leukemic stem cells (LSCs).
- LSC heterogeneity impacts therapy response and disease relapse.
- Understanding LSC diversity is crucial for effective AML treatment.
Purpose of the Study:
- To review the causes and consequences of LSC heterogeneity in AML.
- To highlight advances in single-cell multiomics for dissecting LSC diversity.
- To explore how these technologies can improve AML diagnostics and monitoring.
Main Methods:
- Review of current scientific literature.
- Focus on single-cell multiomics technologies (genomics, transcriptomics, epigenomics, proteomics).
- Analysis of LSC heterogeneity and plasticity in AML.
Main Results:
- LSC heterogeneity arises from genetic and non-genetic factors.
- Single-cell multiomics provides high-resolution molecular snapshots of individual LSCs.
- This technology enables a deeper understanding of LSC states and vulnerabilities.
Conclusions:
- LSC heterogeneity presents challenges but also therapeutic opportunities in AML.
- Single-cell multiomics is transforming the study of AML LSC diversity.
- Advances in these technologies promise to revolutionize AML diagnostics and patient monitoring.
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