Evidence map›Paper›PMID 41472850›Full record

ArticleiMeta2025

Homoharringtonine suppresses acute myeloid leukemia progression by orchestrating EWSR1 phase separation in an m

Ting-Ting Liu, Li-Ting Chen, Xu-Ying Pei, Shao-Nan Hu, Fang-Fang Zhuo, Ze-Kun Chen, Yang Liu, Jing-Kang Wang, Ji-Chao Zhang, Qi Cao and 8 more

Abstract read
In one paragraph

Article in iMeta, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

18 authors.

Ting-Ting LiuState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences Peking University Beijing China.
Li-Ting ChenYunnan Baiyao International Medical Research Center, International Cancer Institute and State Key Laboratory of Molecular Oncology, MOE Frontiers Science Center for Cancer Integrative Omics, School of Basic Medical Sciences Peking University Beijing China.
Xu-Ying PeiPeking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Cell and Gene Therapy for Hematologic Malignancies, Peking University Beijing China.
Shao-Nan HuCollege of Pharmacy Inner Mongolia Medical University Hohhot China.
Fang-Fang ZhuoState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences Peking University Beijing China.
Ze-Kun ChenState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences Peking University Beijing China.
Yang LiuCenter of Basic Medical Research, Institute of Medical Innovation and Research Peking University Third Hospital Beijing China.
Jing-Kang WangState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences Peking University Beijing China.
Ji-Chao ZhangState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences Peking University Beijing China.
Qi CaoYunnan Baiyao International Medical Research Center, International Cancer Institute and State Key Laboratory of Molecular Oncology, MOE Frontiers Science Center for Cancer Integrative Omics, School of Basic Medical Sciences Peking University Beijing China.
Ling LiState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences Peking University Beijing China.
Jing WangState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences Peking University Beijing China.
Tian-Tian WeiState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences Peking University Beijing China.
Bo HanSchool of Pharmacy/Key Laboratory of Xinjiang Phytomedicine Resource and Utilization Shihezi University Shihezi China.
Peng-Fei TuState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences Peking University Beijing China.
Xiang-Yu ZhaoPeking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Cell and Gene Therapy for Hematologic Malignancies, Peking University Beijing China.
Ruidong XueState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences Peking University Beijing China.
Ke-Wu ZengState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences Peking University Beijing China.ORCID https://orcid.org/0000-0003-1082-6327

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Homoharringtonine (HHT) is widely used in combination regimens for acute myeloid leukemia (AML), yet its direct cellular targets remain undefined, limiting precision application. Here, we identified EWS RNA-binding protein 1 (EWSR1) as the primary target of HHT through chemical proteomics and biophysical validation. HHT bound the RNA recognition motif of EWSR1 with micromolar affinity, inducing an allosteric conformational switch that promoted oligomerization and liquid-liquid phase separation (LLPS). EWSR1 condensates selectively recruited the N

Indexed as

acute myeloid leukemiaEWSR1homoharringtonineN6‐methyladenosinephase separationYTHDF2

Identifiers

PMID41472850
PMCPMC12747546

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.