Evidence map›Paper›PMID 26383973›Full record

ArticleCell death and differentiation2016

Rint1 inactivation triggers genomic instability, ER stress and autophagy inhibition in the brain.

P Grigaravicius, E Kaminska, C A Hübner, P J McKinnon, A von Deimling, P-O Frappart

Open access · bronzeAbstract read
In one paragraph

Article in Cell death and differentiation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Phenotype and Long-Term Outcome in Recurrent Paediatric Acute Liver Failure: Systematic Review and Individual Participant Data Analysis.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Pooled it
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  9. RINT1 Loss Impairs Retinogenesis Through TRP53-Mediated Apoptosis.Frontiers in cell and developmental biology · 2020
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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

6 authors at 4 institutions in 2 countries.

P GrigaraviciusClinical Cooperation Unit Neuropathology, German Cancer Research Center (DKFZ), Heidelberg and Consortium for Translational Cancer Research (DKTK), Heidelberg, Germany.
E KaminskaClinical Cooperation Unit Neuropathology, German Cancer Research Center (DKFZ), Heidelberg and Consortium for Translational Cancer Research (DKTK), Heidelberg, Germany.
C A HübnerInstitute of Human Genetics, University Hospital Jena, Friedrich Schiller University, Jena, Germany.
P J McKinnonDepartment of Genetics, St Jude Children's Research Hospital, Memphis, TN, USA.
A von DeimlingClinical Cooperation Unit Neuropathology, German Cancer Research Center (DKFZ), Heidelberg and Consortium for Translational Cancer Research (DKTK), Heidelberg, Germany.
P-O FrappartClinical Cooperation Unit Neuropathology, German Cancer Research Center (DKFZ), Heidelberg and Consortium for Translational Cancer Research (DKTK), Heidelberg, Germany.
German Cancer Research Center · DEFriedrich Schiller University Jena · DEHeidelberg University · DESt. Jude Children's Research Hospital · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
The DNA Damage Response and Tumorigenesis in the BrainP01CA096832 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI BAKER, SUZANNE J. · 2003 to 2025
$38.0M
ATM and DNA Damage in the Nervous SystemR01NS037956 · NINDS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI MCKINNON, PETER J · 1998 to 2022
$7.6M
NCI NIH HHS P01 CA096832NCI NIH HHS P30 CA021765NINDS NIH HHS R01 NS037956
6 · The paper itself

Abstract

Endoplasmic reticulum (ER) stress, defective autophagy and genomic instability in the central nervous system are often associated with severe developmental defects and neurodegeneration. Here, we reveal the role played by Rint1 in these different biological pathways to ensure normal development of the central nervous system and to prevent neurodegeneration. We found that inactivation of Rint1 in neuroprogenitors led to death at birth. Depletion of Rint1 caused genomic instability due to chromosome fusion in dividing cells. Furthermore, Rint1 deletion in developing brain promotes the disruption of ER and Cis/Trans Golgi homeostasis in neurons, followed by ER-stress increase. Interestingly, Rint1 deficiency was also associated with the inhibition of the autophagosome clearance. Altogether, our findings highlight the crucial roles of Rint1 in vivo in genomic stability maintenance, as well as in prevention of ER stress and autophagy.

Indexed as

AutophagyEndoplasmic Reticulum StressGenomic InstabilityAnimalsApoptosisBrainCells, CulturedMice, 129 StrainMice, TransgenicMitosisNeural Stem CellsPrimary Cell CulturePurkinje CellsTumor Suppressor ProteinsVesicular Transport ProteinsRINT-1 protein, mouseTumor Suppressor ProteinsVesicular Transport Proteins

Identifiers

PMID26383973
PMCPMC5072440
OpenAlexW2330644998

What OpenQuestion holds

Textmetadata
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.