Evidence map›Paper›PMID 39964763›Full record

ArticleThe Journal of clinical investigation2025

Reduced EIF6 dosage attenuates TP53 activation in models of Shwachman-Diamond syndrome.

Usua Oyarbide, Valentino Bezzerri, Morgan Staton, Christian Boni, Arish Shah, Marco Cipolli, Eliezer Calo, Seth J Corey

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

8 authors.

Usua OyarbideDepartments of Pediatrics and Cancer Biology, Cleveland Clinic, Cleveland, Ohio, USA.
Valentino BezzerriCystic Fibrosis Center, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
Morgan StatonDepartments of Pediatrics and Cancer Biology, Cleveland Clinic, Cleveland, Ohio, USA.
Christian BoniCystic Fibrosis Center, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
Arish ShahDepartment of Biology and David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Marco CipolliCystic Fibrosis Center, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
Eliezer CaloDepartment of Biology and David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Seth J CoreyDepartments of Pediatrics and Cancer Biology, Cleveland Clinic, Cleveland, Ohio, USA.

Funding

Multiscale Modeling of Myelodysplastic SyndromesR01HL128173 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI COREY, SETH JOEL, KIMMEL, MAREK · 2015 to 2019
$3.8M
Mechanisms regulating ribosome assembly and function in stem cells and vertebrate development.R35GM142634 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Eliezer Calo-Velazquez · 2021 to 2026
$2.3M
Genetic Dissection of Stress Responses in Shwachman-Diamond SyndromeR01DK132812 · NIDDK · CLEVELAND CLINIC LERNER COM-CWRU · PI COREY, SETH JOEL · 2023 to 2025
$701k
Genetic Modifiers for Cancer Stem Cells in Secondary MDS/AMLR21CA159203 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI COREY, SETH JOEL · 2014 to 2015
$374k
NCI NIH HHS R21 CA159203NHLBI NIH HHS R01 HL128173NIDDK NIH HHS R01 DK132812NIGMS NIH HHS R35 GM142634
6 · The paper itself

Abstract

Shwachman-Diamond syndrome (SDS) is characterized by neutropenia, exocrine pancreatic insufficiency, and bony abnormalities with an increased risk of myeloid neoplasia. Almost all cases of SDS result from biallelic mutations in Shwachman-Bodian-Diamond syndrome (SBDS). SBDS interacts with elongation factor-like 1 (EFL1) to displace eukaryotic initiation factor 6 (EIF6) from the 60S ribosomal subunit. Released EIF6 permits the assembly of ribosomal large and small subunits in the cytoplasm. Decreased EIF6 levels due to haploinsufficiency or missense mutations, which lead to decreased protein expression, may provide a somatic genetic rescue and antileukemic effects. We observed accumulation of EIF6 protein in sbds-KO zebrafish models, confirmed this accumulation in patient-derived tissues, and correlated these with changes in ribosomal proteins and tumor protein p53 (TP53) pathways. The mechanism of action for this adaptive response is unknown. To address this, we generated eif6-KO zebrafish, which do not survive more than 10 days after fertilization. We also created 2 mutants with low Eif6 expression, i.e., 5%-25% of WT levels, that could survive until adulthood. We bred them with sbds-null strains and analyzed their phenotype and biochemical properties. Low Eif6 levels reduced Tp53 pathway activation but did not rescue neutropenia in Sbds-deficient zebrafish. Further studies elucidating the interplay between SBDS, EIF6, and TP53 and cellular stress responses offer promising insights into SDS pathogenesis, somatic genetic rescue, and therapeutic strategies.

Indexed as

Anemia, MacrocyticBone Marrow DiseasesExocrine Pancreatic InsufficiencyGene DosageLipomatosisPeptide Initiation FactorsTumor Suppressor Protein p53Zebrafish ProteinsAnimalsDisease Models, AnimalEukaryotic Initiation FactorsGene Knockout TechniquesHaploinsufficiencyHumansProteinsRibosomal ProteinseIF-6EIF6 protein, humanEukaryotic Initiation FactorsPeptide Initiation FactorsProteinsRibosomal ProteinsSBDS protein, humanTP53 protein, humantp53 protein, zebrafishTumor Suppressor Protein p53Zebrafish ProteinsBone marrowGeneticsHematologyLeukemiasNeutrophilsOncology

Identifiers

PMID39964763
PMCPMC11996912

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LicenceCC BY
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Registered trials

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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.