Single‐cell transcriptome profiling reveals blast cell heterogeneity and identifies novel therapeutic target <scp>IKZF2</scp> in t(8;21) acute myeloid leukaemia

The t(8;21)(q22;q22) translocation is one of the most recurrent cytogenetic aberrations in acute myeloid leukaemia (AML). While most patients achieve complete remission, approximately 40% of them still relapse. Early identification and elimination of leukaemia clones with relapse potential could improve prognosis for t(8;21) AML patients. Here, through single-cell RNA sequencing, we characterized the intra-tumoral heterogeneity of t(8;21) AML and identified haematopoietic stem cell (HSC)-like subset as the most quiescent and primitive subgroup among all leukaemia cell populations. Further investigations revealed IKZF2 as the master regulator for HSC-like subset. Notably, IKZF2 was upregulated in t(8;21) AML compared with other AML subtypes and was specifically targeted by AML1-ETO. Using primary samples and mouse models, we verified the high enrichment of IKZF2 in primitive and quiescent leukaemic cells. Moreover, IKZF2 knockout hindered the accumulation of aberrant stem cells driven by AML1-ETO and promoted cellular differentiation both in vitro and in vivo. These facilitate a better understanding of the leukaemia cell heterogeneity in t(8;21) AML and unveil IKZF2 as a potential target for improving current treatment strategies.

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Publication Details

Journal
British Journal of Haematology
Published
2025-08-08
DOI
https://doi.org/10.1111/bjh.70077
Citations
1
Primary Topic
Acute Myeloid Leukemia Research
Type
article
Field-Weighted Citation Impact
1.77

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article

Single‐cell transcriptome profiling reveals blast cell heterogeneity and identifies novel therapeutic target IKZF2 in t(8;21) acute myeloid leukaemia

Junli Mou, Wanqing Xie, Manling Chen, Shaowei Qiu et al.
1 citations
British Journal of Haematology
Acute Myeloid Leukemia Research
1.77
article

Single‐cell transcriptome profiling reveals blast cell heterogeneity and identifies novel therapeutic target IKZF2 in t(8;21) acute myeloid leukaemia

Junli Mou, Wanqing Xie, Manling Chen, Shaowei Qiu, Yihan Mei, Hui Wei, Qing Rao, Jianxiang Wang, Haiyan Xing, Min Wang, Ying Wang, Wei Liu, Qianqian Huang, Shangshang Wang, Runxia Gu, Xiaoyu Liu, Tian Zheng, Kejing Tang, Chengcai Guo, Yu Liu
article en
1 citations

Abstract

The t(8;21)(q22;q22) translocation is one of the most recurrent cytogenetic aberrations in acute myeloid leukaemia (AML). While most patients achieve complete remission, approximately 40% of them still relapse. Early identification and elimination of leukaemia clones with relapse potential could improve prognosis for t(8;21) AML patients. Here, through single-cell RNA sequencing, we characterized the intra-tumoral heterogeneity of t(8;21) AML and identified haematopoietic stem cell (HSC)-like subset as the most quiescent and primitive subgroup among all leukaemia cell populations. Further investigations revealed IKZF2 as the master regulator for HSC-like subset. Notably, IKZF2 was upregulated in t(8;21) AML compared with other AML subtypes and was specifically targeted by AML1-ETO. Using primary samples and mouse models, we verified the high enrichment of IKZF2 in primitive and quiescent leukaemic cells. Moreover, IKZF2 knockout hindered the accumulation of aberrant stem cells driven by AML1-ETO and promoted cellular differentiation both in vitro and in vivo. These facilitate a better understanding of the leukaemia cell heterogeneity in t(8;21) AML and unveil IKZF2 as a potential target for improving current treatment strategies.

British Journal of HaematologyVol. 207(4)
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital (CN), Institute of Hematology & Blood Diseases Hospital (CN)
National Natural Science Foundation of China, Tianjin Science and Technology Committee, National Key Research and Development Program of China
Good health and well-being
Openalex Percentile: Top 14%
Acute Myeloid Leukemia Research
1.77
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