Evidence map›Paper›PMID 41708874›Full record

ReviewThe EMBO journal2026

eIF3 musketeers: loyal in health, rogue in disease, and redeemed by therapeutic targeting.

Reza Mohammadinejad, Dan Su, Fanglin Luo, Mengyu Li, Haoran Duan, Jing Wang, Fajin Li, Michal Shapira, Dieter A Wolf

Abstract readReview
In one paragraph

Review in The EMBO journal, 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

9 authors.

Reza MohammadinejadWestlake Laboratory of Life Sciences and Biomedicine, Hangzhou, China. r.mohammadinejad@westlake.edu.cn.ORCID http://orcid.org/0000-0003-3511-9282
Dan SuSchool of Medicine, Westlake University, Hangzhou, China.ORCID http://orcid.org/0009-0002-3964-7701
Fanglin LuoSchool of Medicine, Westlake University, Hangzhou, China.ORCID http://orcid.org/0009-0007-6403-5148
Mengyu LiSchool of Medicine, Westlake University, Hangzhou, China.ORCID http://orcid.org/0009-0001-6786-858X
Haoran DuanSchool of Medicine, Westlake University, Hangzhou, China.ORCID http://orcid.org/0009-0004-8761-7878
Jing WangSchool of Medicine, Westlake University, Hangzhou, China.ORCID http://orcid.org/0009-0009-3075-9177
Fajin LiSchool of Medicine, Westlake University, Hangzhou, China.ORCID http://orcid.org/0000-0001-8101-0478
Michal ShapiraDepartment of Life Sciences, Ben-Gurion University, Beer Sheva, Israel.ORCID http://orcid.org/0000-0002-6164-7874
Dieter A WolfWestlake Laboratory of Life Sciences and Biomedicine, Hangzhou, China. dawolf@westlake.edu.cn.ORCID http://orcid.org/0000-0002-3761-1070

Funding

Deutsche Forschungsgemeinschaft (DFG) 506550226Israel Science Foundation (ISF) 471/2021MOST | National Natural Science Foundation of China (NSFC) W2531017Westlake Laboratory of Life Sciences and Biomedicine 2024SSYS0029
6 · The paper itself

Abstract

The eukaryotic translation initiation factor 3 (eIF3) is the largest and most complex initiation factor in eukaryotes, functioning as a central hub that integrates signals from cellular stress, metabolism, and developmental pathways to regulate mRNA translation. Recent advances have uncovered subunit-specific roles of eIF3 that extend beyond canonical cap-dependent translation to include specialized mechanisms such as selective mRNA recruitment, noncanonical cap recognition, and translation elongation. This review summarizes the current mechanistic understanding of the contribution of aberrant eIF3 activity to diverse disease processes, including oncogenesis, neurodevelopmental and neurodegenerative disorders, muscle pathology, and infectious disease. We evaluate therapeutic strategies aimed at modulating eIF3 function, including subunit-selective small molecules, RNA-based therapeutics, and CRISPR-based interventions. We discuss the therapeutic promise of both inhibitory approaches-targeting oncogenic or pathogen-hijacked eIF3-and restorative strategies to correct genetic loss-of-function in neurological disease. Finally, we outline key challenges and opportunities for clinical translation, including tissue-specific delivery, subunit selectivity, and the identification of predictive biomarkers. eIF3 emerges as a versatile and druggable node in translational control with broad relevance across human disease.

Indexed as

Eukaryotic Initiation Factor-3AnimalsHumansNeoplasmsNeurodegenerative DiseasesProtein BiosynthesisEukaryotic Initiation Factor-3CancerInfectious DiseaseNeurodevelopmental DisordersTargeted TherapyTranslation initiation factor eIF3

Identifiers

PMID41708874
PMCPMC13044287

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.