# Defining the role of natural killer cells in acute myeloid leukemia through the lens of single-cell omics

**Authors:** Chen Liang, Meichi Yue, Kehui Zhang, Sining Zhou, Xiaojing Xu, Shiwei Wang, Shiping Liu

PMC · DOI: 10.3389/fimmu.2026.1734327 · Frontiers in Immunology · 2026-01-30

## TL;DR

This review explores how natural killer cells are affected in acute myeloid leukemia and how single-cell omics can improve understanding and treatment.

## Contribution

The paper systematically examines NK cell dysfunction in AML using single-cell omics and highlights potential immunotherapies.

## Key findings

- NK cells in AML show functional deficiencies that hinder tumor surveillance.
- Single-cell omics reveals altered receptor expression and cytokine profiles in AML NK cells.
- Modulating NK cells could enhance immunotherapy outcomes in AML.

## Abstract

This review explores the alterations in natural killer (NK) cell function in acute myeloid leukemia (AML) and their implications for disease progression and therapeutic outcomes. As key effectors of innate immunity, NK cells are critical in recognizing and eliminating malignant cells. In AML, however, NK cells frequently exhibit numerical and functional deficiencies, resulting in compromised immunosurveillance that facilitates tumor immune escape and disease advancement. We systematically examine the application of single-cell omics technologies in AML research to elucidate the omics profiles and phenotypic distribution of NK cells within the leukemic microenvironment, characterizing their dysfunctional state by upregulated inhibitory receptors, downregulated activating signals, an altered cytokine milieu, and complex cellular crosstalk within the bone marrow (BM) niche. Furthermore, this article correlates functional dynamics of NK cells with conventional and emerging treatments, including CAR-NK immunotherapy, underscoring their potential role in disease monitoring and prognostic stratification. We also discuss promising NK cell-based immunotherapeutic strategies for AML, emphasizing the potential of modulating or engineering NK cells to enhance antitumor immunity. A deeper understanding of NK cell biology and regulatory mechanisms in AML is essential for developing novel immunotherapies and improving patient prognosis.

## Linked entities

- **Diseases:** acute myeloid leukemia (MONDO:0015667), AML (MONDO:0018874)

## Full-text entities

- **Genes:** CXADRP1 (CXADR pseudogene 1) [NCBI Gene 653108] {aka CAR, CXADRP}
- **Diseases:** tumor (MESH:D009369), AML (MESH:D015470), leukemic (MESH:D007938)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

140 references — full list in the complete paper: https://tomesphere.com/paper/PMC12901400/full.md

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Source: https://tomesphere.com/paper/PMC12901400