Evidence map›Paper›PMID 42277036›Full record

ArticleNature communications2026

Targeting SMC3 deacetylation synergizes with XPO1 inhibition to reprogram the epigenetic landscape and suppress NPM1-mutated acute myeloid leukemia.

Jianfeng Fu, Huilin Xu, Xinying Zhao, Mengge Gao, Yonglu Tian, Yingjun Chang, Xiaofeng Zheng

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jianfeng Fu *State Key Laboratory of Gene Function and Modulation Research, School of Life Sciences, Peking University, Beijing, China.ORCID http://orcid.org/0000-0002-1864-6948
Huilin Xu *State Key Laboratory of Gene Function and Modulation Research, School of Life Sciences, Peking University, Beijing, China.ORCID http://orcid.org/0009-0004-3970-5144
Xinying ZhaoMinistry of Education Key Laboratory of Cell Proliferation and Differentiation, School of Life Sciences, Peking University, Beijing, China.ORCID http://orcid.org/0009-0001-8432-551X
Mengge GaoPeking University People's Hospital and Institute of Hematology, Peking University, Beijing, China.ORCID http://orcid.org/0000-0003-2329-5625
Yonglu TianSchool of Life Sciences, Peking University, Beijing, China.ORCID http://orcid.org/0000-0002-1036-767X
Yingjun ChangPeking University People's Hospital and Institute of Hematology, Peking University, Beijing, China. rmcyj@bjmu.edu.cn.ORCID http://orcid.org/0000-0002-6124-6050
Xiaofeng ZhengState Key Laboratory of Gene Function and Modulation Research, School of Life Sciences, Peking University, Beijing, China. xiaofengz@pku.edu.cn.ORCID http://orcid.org/0000-0001-6790-0669

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32500493National Natural Science Foundation of China (National Science Foundation of China) 82130081 and 32270756
6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a prevalent hematologic malignancy. Mutations in Nucleophosmin (NPM1c) is the most frequent genetic alterations in AML. However, the epigenetic regulatory mechanisms of this AML subtype remain unclear. The cohesin complex, regulated by the acetyltransferase ESCO2, orchestrates chromatin organization and regulates gene expression. Here, we show that loss of ESCO2 promotes the progression of NPM1-mutated AML by destabilizing cohesin and the NuRD complex on chromatin, thereby enhancing the expression of genes associated with leukemia self-renewal capacity. Pharmacological HDAC8 inhibition restores SMC3 binding and induces differentiation and apoptosis in NPM1-mutated AML cells. Simultaneously targeting HDAC8 and nuclear exporter XPO1 reverses aberrant epigenetic landscape and represses self-renewal gene expression induced by ESCO2 deficiency. The combined treatment effectively eliminates NPM1-mutated AML cell lines and primary human AML cells in vitro and in vivo. This study reveals an ESCO2 deficiency-induced aberrant epigenetic landscape via SMC3 hypoacetylation and identifies a potential therapeutic strategy for NPM1-mutated AML.

Indexed as

Cell Cycle ProteinsChromosomal Proteins, Non-HistoneEpigenesis, GeneticKaryopherinsLeukemia, Myeloid, AcuteNuclear ProteinsReceptors, Cytoplasmic and NuclearAcetylationAcetyltransferasesAnimalsApoptosisCell Line, TumorExportin 1 ProteinHistone DeacetylasesHumansHydrazinesAcetyltransferasesCell Cycle ProteinsChromosomal Proteins, Non-HistoneExportin 1 ProteinHDAC8 protein, humanHistone DeacetylasesHydrazinesKaryopherinsNPM1 protein, humanNpm1 protein, mouseNuclear ProteinsNucleophosminReceptors, Cytoplasmic and NuclearRepressor ProteinsselinexorTriazoles

Identifiers

PMID42277036
PMCPMC13408497

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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.