Evidence map›Paper›PMID 26485546›Full record

ArticleTranslational psychiatry2015

Increased abundance of translation machinery in stem cell-derived neural progenitor cells from four schizophrenia patients.

A Topol, J A English, E Flaherty, P Rajarajan, B J Hartley, S Gupta, F Desland, S Zhu, T Goff, L Friedman and 10 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
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

31 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Network-based drug repurposing for schizophrenia.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Protein Translation and Psychiatric Disorders.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2020
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

20 authors at 7 institutions in 3 countries.

A TopolDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
J A EnglishRoyal College of Surgeons in Ireland, Beaumont Hospital, Beaumont, Dublin, Ireland.
E FlahertyDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
P RajarajanDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
B J HartleyDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
S GuptaDepartment of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH, USA.
F DeslandDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
S ZhuDepartment of Genetics and Genomics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
T GoffDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
L FriedmanChildhood Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA.
J RapoportChildhood Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA.
D FelsenfeldDepartment of Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
G CagneyUCD Conway Institute of Biomolecular and Biomedical Research, Dublin, Ireland.
A Mackay-SimEskitis Institute for Drug Discovery, Griffith University, Brisbane, QLD, Australia.
J N SavasDepartment of Chemical Physiology, The Scripps Research Institute, La Jolla, CA, USA.
B AronowDepartment of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH, USA.
G FangDepartment of Genetics and Genomics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
B ZhangDepartment of Genetics and Genomics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
D CotterRoyal College of Surgeons in Ireland, Beaumont Hospital, Beaumont, Dublin, Ireland.
K J BrennandDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Icahn School of Medicine at Mount Sinai · USCincinnati Children's Hospital Medical Center · USNational Institute of Mental Health · USBeaumont Hospital · IEGriffith University · AURoyal College of Surgeons in Ireland · IEScripps Research Institute · US

Funding

Higher Order Chromatin and Genetic Risk for SchizophreniaR01MH106056 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI AKBARIAN, SCHAHRAM, BRENNAND, KRISTEN JENNIFER · 2015 to 2023
$6.7M
Contrasting causal microRNAs in forebrain and midbrain COS hiPSC neural cellsR01MH101454 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BRENNAND, KRISTEN JENNIFER · 2013 to 2017
$2.8M
Proteome Biology of Noise Induced Hearing LossR00DC013805 · NIDCD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SAVAS, JEFFREY NICHOLAS · 2015 to 2017
$747k
NIDCD NIH HHS R00 DC013805NIDCD NIH HHS R00DC013805-02NIMH NIH HHS R01 MH101454NIMH NIH HHS R01 MH106056NIMH NIH HHS U19 MH194172
6 · The paper itself

Abstract

The genetic and epigenetic factors contributing to risk for schizophrenia (SZ) remain unresolved. Here we demonstrate, for the first time, perturbed global protein translation in human-induced pluripotent stem cell (hiPSC)-derived forebrain neural progenitor cells (NPCs) from four SZ patients relative to six unaffected controls. We report increased total protein levels and protein synthesis, together with two independent sets of quantitative mass spectrometry evidence indicating markedly increased levels of ribosomal and translation initiation and elongation factor proteins, in SZ hiPSC NPCs. We posit that perturbed levels of global protein synthesis in SZ hiPSC NPCs represent a novel post-transcriptional mechanism that might contribute to disease progression.

Indexed as

Cell DifferentiationCells, CulturedHumansInduced Pluripotent Stem CellsNeural Stem CellsNeuronsProsencephalonSchizophrenia

Identifiers

PMID26485546
PMCPMC4930118
OpenAlexW1763415643

What OpenQuestion 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 OpenQuestion graph.