Evidence map›Paper›PMID 40102796›Full record

ArticleBMC cancer2025

Establishment of CD34 + hematopoietic stem cell-derived xenograft model of hyperleukocytic acute myeloid leukemia.

Yanxia Jin, Yuxing Liang, Balu Wu, Sanyun Wu, Xiaoyan Liu, Fuling Zhou

Abstract read
In one paragraph

Article in BMC cancer, 2025. 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

6 authors.

Yanxia Jin *Department of Haematology, Zhongnan Hospital, Wuhan University, Wuhan, 430071, Hubei, China.
Yuxing Liang *Department of Haematology, Zhongnan Hospital, Wuhan University, Wuhan, 430071, Hubei, China.
Balu WuDepartment of Haematology, Zhongnan Hospital, Wuhan University, Wuhan, 430071, Hubei, China.
Sanyun WuDepartment of Haematology, Zhongnan Hospital, Wuhan University, Wuhan, 430071, Hubei, China.
Xiaoyan LiuDepartment of Haematology, Zhongnan Hospital, Wuhan University, Wuhan, 430071, Hubei, China. liuxiaoyan@znhospital.cn.
Fuling ZhouDepartment of Haematology, Zhongnan Hospital, Wuhan University, Wuhan, 430071, Hubei, China. zhoufuling@whu.edu.cn.

Funding

Hubei Province key research and development plan No. CZKYXM2023036JZNatural Science Foundation of China (NSFC) programme No. 82370176
6 · The paper itself

Abstract

backgroundHyperleukocytic acute myeloid leukemia (HLL) is marked by high early mortality and presents significant therapeutic challenges. Research on HLL is still in its infancy, and comprehensive development of patient-derived xenograft (PDX) models, especially CD34 + hematopoietic stem cell-derived models, remains limited.

methodsWe evaluated the establishment of the HLL model through blood examinations, smear analysis, bone marrow biopsy, flow cytometry, and mutation analysis. Correlation between survival times in mice and patients was assessed using linear regression.

resultsIn the HLL PDX mouse model, leukocyte counts could reach up to 37.35^10⁹/L, and immunophenotyping revealed the presence of hCD45+, hCD15+, and hCD33 + cells in both peripheral blood (PB) and bone marrow (BM) following inoculation with PB-derived cells for the establishment of the HLL PDX model. Similar results were observed with cells derived from the patient's BM. In the CD34 + hematopoietic stem cell-derived xenograft model, extensive infiltration of CD34 + cells into the BM, liver, and spleen was observed. Additionally, human WT1 and NRAS mutations were identified in the liver, spleen, and BM of the mice. A comparative analysis of multiple experiments revealed that shorter survival times were observed in mice receiving a higher irradiation dose of 2.5 Gy and a greater number of cells derived from PB. Additionally, shorter survival times were observed in model mice injected with cells carrying NRAS, DNMT3A, FLT3, or NPM1 gene mutations. Correlation analysis indicated that the survival times of the mice were significantly associated with the survival status of the patients.

conclusionsWe successfully established a CD34 + hematopoietic stem cell-derived xenograft model of HLL, providing a valuable tool for mechanistic research, drug screening, individualized therapy, and precision medicine.

trial registrationNot application.

Indexed as

Antigens, CD34Hematopoietic Stem CellsLeukemia, Myeloid, AcuteAdultAnimalsDisease Models, AnimalFemaleHematopoietic Stem Cell TransplantationHumansMaleMiceMiddle AgedMutationNucleophosminAntigens, CD34NPM1 protein, humanNpm1 protein, mouseNucleophosminB-NSG miceCD34 + hematopoietic stem cellHyperleukocytic acute myeloid leukemiaPatient-derived xenograft model

Identifiers

PMID40102796
PMCPMC11917077

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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.