Evidence map›Paper›PMID 41559783›Full record

ArticleExperimental hematology & oncology2026

ELK1 promotes the progress of myeloid leukemia by hindering the differentiation of neutrophils.

Yuhan He, Ya Zhou, Dexin Wen, Rongqun Guo, Juan Du, Sizhou Huang, Yong Dong

Abstract read
In one paragraph

Article in Experimental hematology & oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Yuhan He *Department of Immunology, School of Basic Medical Sciences, Chengdu Medical College, Xindu Road 783, Chengdu, 610500, China.
Ya Zhou *Cell and Gene Therapy Center, Institute of Blood Transfusion, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Chengdu, China.
Dexin Wen *Department of Immunology, School of Basic Medical Sciences, Chengdu Medical College, Xindu Road 783, Chengdu, 610500, China.
Rongqun GuoPublic Research Platform Management Center/ Translational Medical Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Juan DuDepartment of Hematology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
Sizhou HuangDepartment of Anatomy and Histology and Embryology, School of Basic Medical Sciences, Chengdu Medical College, Chengdu, China.
Yong DongDepartment of Immunology, School of Basic Medical Sciences, Chengdu Medical College, Xindu Road 783, Chengdu, 610500, China. dongyong@cmc.edu.cn.

Funding

Advanced Talents Training Program of Chengdu Medical College KYPY22-01CAMS Initiatives for Innovative Medicine 2021-I2M-1-060CMC Excellent-talent program 2024yxGzn03National Key Research and Development Program of China 2023YFC3403802National Natural Science Foundation of China 82470122 and 82200127National Natural Science Foundation of China 82470125
6 · The paper itself

Abstract

backgroundThe genes controlling lineage determination and differentiation tend to be essential for the development of acute myeloid leukemia (AML). Identifying novel target genes capable of promoting the differentiation and maturation of undifferentiated leukemia cells offers a promising therapeutic strategy for the treatment of AML.

methodsWe used conditional Elk1 and KrasG12D expression mice, along with Mx1-Cre, Lyz2-Cre and Elane-Cre drive strains (which enable stage specific control of Elk1 or KrasG12D expression), to investigate the function of Elk1 in the hematopoiesis and leukemogenesis. Bone marrow transplantation assay was performed to explore the function of Elk1 in hematopoiesis under stress conditions. Additionally, bulk-cell RNA sequencing, single-cell RNA sequencing and proteomics were performed to reveal the signaling pathways altered by Elk1. Finally, undifferentiated leukemia cells were used to verify whether inhibiting ELK1 could promote the differentiation of these cells into mature neutrophils.

resultsELK1 is highly expressed in undifferentiated AML cells. Studies using mouse model demonstrated that overexpression of Elk1 accelerates the development of KrasG12D-induced myeloid leukemia by impairing the stemness of hematopoietic stem cells (HSCs) and impeding the differentiation of neutrophils. Furthermore, impeding the maturation of neutrophils independently promotes the development of KrasG12D mutation-induced myeloid leukemia. Meanwhile, our in vitro experiments preliminarily confirmed that inhibiting ELK1 suppresses the proliferation of leukemia cells and induces the differentiation of CD15

conclusionsOur study demonstrates that ELK1 is a potential therapeutic target for AML, due to its critical role in regulating neutrophils differentiation.

Indexed as

ELK1HematopoiesisLeukemogenesisMyeloid leukemiaNeutrophil depletion

Identifiers

PMID41559783
PMCPMC12829227

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.