Xingqi Chen – Studies of the cell fate decision using single-cell technologies
The focus of our work is to understand cell fate decision during development and in human diseases such as cancer. Our aim is to provide a deeper understanding of cancer progression, which may contribute to the development of new treatment strategies.
Recent advances in single-cell technologies such as single-cell ATAC-seq and single-cell RNA-seq have made it possible to explore cellular heterogeneity by profiling epigenetic, transcriptional, and protein-level information at single-cell resolution. However, a cell’s state is determined by a complex interplay of the genome, epigenome, transcriptome and proteome, and analysis of a single molecular layer provides only a partial understanding of cellular identity.
To achieve a comprehensive understanding of cellular heterogeneity, our research aims to integrate multiple layers of molecular information, including nuclear architecture, epigenetics, transcriptomics, and proteomics, from the same individual cell. This will allow reconstructing a detailed regulatory circuitry of cell function and fate.
Mechanisms behind cell fate
The overarching goal of our research is to elucidate the mechanisms governing cell fate decisions during development and in human disease. We are developing state-of-the-art single-cell technologies to systematically characterize cellular heterogeneity and to identify the key regulatory factors that control specific cell fates.
A central question motivating our work is why cells in the human body, despite sharing an identical DNA sequence, adopt markedly different functional identities. For example, what determines why certain cells undergo malignant transformation while others remain normal? Similarly, what molecular mechanisms enable stem cells to differentiate into distinct cell types?
Epigenetic regulation
Our primary objective is to uncover the epigenetic mechanisms that regulate cell fate in the context of human disease, mainly cancer. To address this, we pursue two major research directions:
- Deciphering the tumour microenvironment across multiple primary human cancer types using advanced single-cell technologies.
- Developing novel single-cell platforms to achieve deeper, more accurate, and multi-dimensional cellular analyses.
The insights generated from our research will provide a deeper understanding of cancer progression at the single-cell level and may contribute to the development of novel diagnostic tools and therapeutic strategies. Our long-term goal is to identify actionable molecular targets for precision cancer therapy.
More information on the website: www.chenlabuppsala.com.

Group members
Publications
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Part of Biochemical Pharmacology, 2026
- DOI for Albacarcin V adds EPLIN as a novel and promising target for the treatment of female cancers and pediatric medulloblastoma
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Part of Matrix Biology, p. 1-15, 2025
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Part of Cell Death and Disease, 2025
- DOI for Identification of a small molecule targeting EPLIN as a novel strategy for the treatment of pediatric neuroblastoma and medulloblastoma
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Part of Nature Communications, 2025
- DOI for Precise mapping of single-stranded DNA breaks by sequence-templated erroneous DNA polymerase end-labelling
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Part of Nature Communications, 2025
- DOI for scFFPE-ATAC enables high-throughput single cell chromatin accessibility profiling in formalin-fixed paraffin-embedded samples
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Epigenetic insights into GABAergic development in Dravet Syndrome iPSC and therapeutic implications
Part of eLIFE, 2024
- DOI for Epigenetic insights into GABAergic development in Dravet Syndrome iPSC and therapeutic implications
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Epigenetic regulation of cell state by H2AFY governs immunogenicity in high-risk neuroblastoma
Part of Journal of Clinical Investigation, 2024
- DOI for Epigenetic regulation of cell state by H2AFY governs immunogenicity in high-risk neuroblastoma
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Part of Leukemia, p. 1086-1098, 2024
- DOI for Genome-wide DNA methylation-analysis of blastic plasmacytoid dendritic cell neoplasm identifies distinct molecular features
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Part of PLoS Pathogens, 2024
- DOI for Porcine circovirus type 2 infection promotes the SUMOylation of nucleophosmin-1 to facilitate the viral circular single-stranded DNA replication
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Part of Cell Reports, 2023
- DOI for Epiblast-like stem cells established by Wnt/β-catenin signaling manifest distinct features of formative pluripotency and germline competence
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Heparanase Modulates Chromatin Accessibility
Part of Cells, 2023
- DOI for Heparanase Modulates Chromatin Accessibility
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Identification of ATF3 as a novel protective signature of quiescent colorectal tumor cells
Part of Cell Death and Disease, 2023
- DOI for Identification of ATF3 as a novel protective signature of quiescent colorectal tumor cells
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A Highly Sensitive Method to Efficiently Profile the Histone Modifications of FFPE Samples
Part of Bio-protocol, 2022
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BRD2 compartmentalizes the accessible genome
Part of Nature Genetics, p. 481-491, 2022
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Part of Nature Communications, 2022
- DOI for Cell-lineage controlled epigenetic regulation in glioblastoma stem cells determines functionally distinct subgroups and predicts patient survival
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Dormant SOX9-Positive Cells Facilitate MYC-Driven Recurrence of Medulloblastoma
Part of Cancer Research, p. 4586-4603, 2022
- DOI for Dormant SOX9-Positive Cells Facilitate MYC-Driven Recurrence of Medulloblastoma
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Epigenomic priming of immune genes implicates oligodendroglia in multiple sclerosis susceptibility
Part of Neuron, p. 1193-1210, 2022
- DOI for Epigenomic priming of immune genes implicates oligodendroglia in multiple sclerosis susceptibility
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Part of Physical Review B, 2022
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Part of Current Protocols, 2022
- DOI for FFPE-ATAC: A Highly Sensitive Method for Profiling Chromatin Accessibility in Formalin-Fixed Paraffin-Embedded Samples
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Part of Physical Review B, 2022
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Profiling chromatin accessibility in formalin-fixed paraffin-embedded samples
Part of Genome Research, p. 150-161, 2022
- DOI for Profiling chromatin accessibility in formalin-fixed paraffin-embedded samples
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Part of Journal of Investigative Dermatology, p. 705-716, 2022
- DOI for Single-Cell Analysis Reveals Major Histocompatibility Complex II-Expressing Keratinocytes in Pressure Ulcers with Worse Healing Outcomes
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Super-enhancers conserved within placental mammals maintain stem cell pluripotency
Part of Proceedings of the National Academy of Sciences of the United States of America, 2022
- DOI for Super-enhancers conserved within placental mammals maintain stem cell pluripotency
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Part of Nucleic Acids Research, 2021
- DOI for FACT-seq: profiling histone modifications in formalin-fixed paraffin-embedded samples with low cell numbers
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Part of Nature Communications, 2021
- DOI for Focal amplifications are associated with chromothripsis events and diverse prognoses in gastric cardia adenocarcinoma
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Part of The FASEB Journal, 2021
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Part of Physical Review B, 2021
- DOI for Structural phase transition in monolayer gold(I) telluride: From a room-temperature topological insulator to an auxetic semiconductor
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Super enhancers-Functional cores under the 3D genome
Part of Cell Proliferation, 2021
- DOI for Super enhancers-Functional cores under the 3D genome
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Part of Omics, p. 652-659, 2021
- DOI for The Thioesterase ACOT1 as a Regulator of Lipid Metabolism in Type 2 Diabetes Detected in a Multi-Omics Study of Human Liver
- Download full text (pdf) of The Thioesterase ACOT1 as a Regulator of Lipid Metabolism in Type 2 Diabetes Detected in a Multi-Omics Study of Human Liver
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3D ATAC-PALM: super-resolution imaging of the accessible genome
Part of Nature Methods, p. 430-436, 2020
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Circular ecDNA promotes accessible chromatin and high oncogene expression
Part of Nature, p. 699-703, 2019