Evidence map›Paper›PMID 40971057›Full record

ArticleMedical oncology (Northwood, London, England)2025

Synergy Between second-generation FLT3 inhibitors and the ERK1/2 inhibitor Ulixertinib in FLT3-ITD-mutated acute myeloid leukemia (AML) cells.

Daniel Muteb Muyey, Yuanyuan Wang, Shuo Li, Zhuanghui Hao, Jingyi Feng, Fanggang Ren, Hongwei Wang

Abstract read
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In one paragraph

Article in Medical oncology (Northwood, London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Daniel Muteb MuyeyShanxi Medical University, 030001, Taiyuan, People's Republic of China.
Yuanyuan WangShanxi Medical University, 030001, Taiyuan, People's Republic of China.
Shuo LiShanxi Medical University, 030001, Taiyuan, People's Republic of China.
Zhuanghui HaoShanxi Medical University, 030001, Taiyuan, People's Republic of China.
Jingyi FengInstitute of Hematology, Second Hospital of Shanxi Medical University, 030001, Taiyuan, People's Republic of China.
Fanggang RenInstitute of Hematology, Second Hospital of Shanxi Medical University, 030001, Taiyuan, People's Republic of China.
Hongwei WangShanxi Medical University, 030001, Taiyuan, People's Republic of China. wanghw68@hotmail.com.

Funding

Health Commission of Shanxi Province 2021XM07Shanxi Provincial Science and Technology Department YDZJSX2021B009
6 · The paper itself

Abstract

The FLT3 internal tandem duplication (FLT3-ITD) mutation is a critical molecular marker in acute myeloid leukemia (AML) and is closely associated with adverse patient prognosis. Although FLT3 inhibitors have been clinically applied, their therapeutic efficacy is constrained by reduced drug responsiveness and disease relapse. This study aims to investigate the underlying causes of the limited therapeutic efficacy of FLT3 inhibitors in FLT3-ITD-positive AML cells and propose feasible solutions. We screened datasets associated with Gilteritinib and Quizartinib in the Gene Expression Omnibus (GEO) database for enrichment analysis and validated potential key pathways that may limit their therapeutic efficacy through qPCR and Western blot. By assessing proliferation, apoptosis, and cell cycle in MV4-11 and MOLM-13 cells, we verified the combined effects of the ERK1/2 inhibitor Ulixertinib with Gilteritinib or Quizartinib, and further explored the underlying mechanisms via transcriptome sequencing. Gilteritinib and Quizartinib both significantly activated the RAS/MAPK pathway in FLT3-ITD-positive AML cells. While the ERK1/2 inhibitor Ulixertinib alone did not inhibit FLT3-ITD-positive AML cells viability, its combination with Gilteritinib or Quizartinib exhibited potent synergistic effects. Transcriptome sequencing revealed that these synergistic effects may stem from the regulation of gene expression such as PKD1, NR2E3, KDF1, and PRSS8 as well as modulation of ion channel activity. This in vitro study identifies aberrant activation of the RAS/MAPK pathway as a critical factor limiting the efficacy of FLT3 inhibitors in FLT3-ITD-positive AML and demonstrates the potent synergistic effects of Ulixertinib combined with FLT3 inhibitors in FLT3-ITD-positive AML cells, providing a novel therapeutic strategy for AML.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBenzothiazolesfms-Like Tyrosine Kinase 3Leukemia, Myeloid, AcutePhenylurea CompoundsProtein Kinase InhibitorsAniline CompoundsApoptosisCell Line, TumorCell ProliferationDrug SynergismHumansMAP Kinase Signaling SystemMutationPyrazinesAniline CompoundsBenzothiazolesFLT3 protein, humanfms-Like Tyrosine Kinase 3gilteritinibPhenylurea CompoundsProtein Kinase InhibitorsPyrazinesquizartinibAcute myeloid leukemia (AML)ERK1/2 inhibitorFLT3 inhibitorFLT3 internal tandem duplication (FLT3-ITD)RAS/MAPK pathway

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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.