Evidence map›Paper›PMID 36526374›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2023

mTORC2 Inhibition Improves Morphological Effects of PTEN Loss, But Does Not Correct Synaptic Dysfunction or Prevent Seizures.

Erin R Cullen, Kamran Tariq, Amy N Shore, Bryan W Luikart, Matthew C Weston

Open access · greenAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 27 citations in OpenAlex.

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  5. Cell-Intrinsic Regulation of Epilepsy-Associated Pathology by mTORC1 and mTORC2.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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  15. The mTOR pathway genesbioRxiv : the preprint server for biology · 2024
    Article
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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

5 authors at 2 institutions in 1 country.

Erin R CullenDepartment of Neurological Sciences, Larner College of Medicine, University of Vermont, Burlington, Vermont 05405.ORCID 0000-0002-0134-8717
Kamran TariqDepartment of Molecular and Systems Biology, Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire 03755.ORCID 0000-0003-0074-4475
Amy N ShoreDepartment of Neurological Sciences, Larner College of Medicine, University of Vermont, Burlington, Vermont 05405.
Bryan W LuikartDepartment of Molecular and Systems Biology, Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire 03755 bryan.w.luikart@dartmouth.edu matthew.c.weston@med.uvm.edu.ORCID 0000-0002-3181-6075
Matthew C WestonDepartment of Neurological Sciences, Larner College of Medicine, University of Vermont, Burlington, Vermont 05405 bryan.w.luikart@dartmouth.edu matthew.c.weston@med.uvm.edu.ORCID 0000-0001-5558-7070
University of Vermont · USDartmouth College · US

Funding

Vermont Center for Cardiovascular and Brain HealthP20GM135007 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI Kathryn H Morelli · 2020 to 2026
$17.4M
The Impact of PTEN Signaling on Neuronal Form and FunctionR01MH097949 · NIMH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BRYAN W LUIKART · 2012 to 2026
$7.4M
Synaptic changes and hypersynchronous network activity in mTORopathiesR01NS110945 · NINDS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI WESTON, MATTHEW C · 2019 to 2023
$1.7M
Regulation of synapse and network dynamics at MTORR00NS087095 · NINDS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI WESTON, MATTHEW C · 2016 to 2018
$744k
NIGMS NIH HHS P20 GM135007NIMH NIH HHS R01 MH097949NINDS NIH HHS R00 NS087095NINDS NIH HHS R01 NS110945
6 · The paper itself

Abstract

Hyperactivation of PI3K/PTEN-mTOR signaling during neural development is associated with focal cortical dysplasia (FCD), autism, and epilepsy. mTOR can signal through two major hubs, mTORC1 and mTORC2, both of which are hyperactive following PTEN loss of function (LOF). Here, we tested the hypothesis that genetic inactivation of the mTORC2 complex via deletion of

Indexed as

EpilepsySeizuresAnimalsFemaleHomozygoteMaleMechanistic Target of Rapamycin Complex 2MiceMice, KnockoutPhosphatidylinositol 3-KinasesPTEN PhosphohydrolaseSequence DeletionTOR Serine-Threonine KinasesMechanistic Target of Rapamycin Complex 2Phosphatidylinositol 3-KinasesPTEN PhosphohydrolaseTOR Serine-Threonine Kinasesdentate gyrusepilepsymTORmTORC1mTORC2synaptic transmission

Identifiers

PMID36526374
PMCPMC9899090
OpenAlexW4312212116

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.