Evidence map›Paper›PMID 37398196›Full record

ArticleResearch square2023

High-Content Small Molecule Screen Identifies a Novel Compound That Restores AP-4-Dependent Protein Trafficking in Neuronal Models of AP-4-Associated Hereditary Spastic Paraplegia.

Afshin Saffari, Barbara Brechmann, Cedric Boeger, Wardiya Afshar Saber, Hellen Jumo, Dosh Whye, Delaney Wood, Lara Wahlster, Julian Alecu, Marvin Ziegler and 9 more

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2023. 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, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 3 institutions in 2 countries.

Afshin SaffariBoston Children's Hospital, Harvard Medical School.
Barbara BrechmannBoston Children's Hospital, Harvard Medical School.
Cedric BoegerBoston Children's Hospital, Harvard Medical School.
Wardiya Afshar SaberBoston Children's Hospital/Harvard Medical School.ORCID 0000-0001-9488-7893
Dosh WhyeBoston Children's Hospital, Harvard Medical School.ORCID 0000-0002-6895-9627
Delaney WoodBoston Children's Hospital, Harvard Medical School.
Lara WahlsterBoston Children's Hospital, Harvard Medical School.
Julian AlecuBoston Children's Hospital, Harvard Medical School.
Marvin ZieglerHarvard Medical School.ORCID 0000-0002-0504-7815
Marlene ScheffoldBoston Children's Hospital, Harvard Medical School.
Kellen WindenBoston Children's Hospital.
Jed HubbsBoston Children's Hospital.
Elizabeth ButtermoreBoston Children's Hospital.ORCID 0000-0003-3194-5413
Lee BarrettBoston Children's Hospital.
Georg BornerMax Planck Institute of Biochemistry.ORCID 0000-0002-3166-3435
Alexandra DaviesMax Planck Institute of Biochemistry.ORCID 0000-0002-1594-8780
Mustafa SahinBoston Children's Hospital.ORCID 0000-0001-7044-2953
Darius Ebrahimi-FakhariBoston Children's Hospital, Harvard Medical School.ORCID 0000-0002-0026-4714
Boston Children's Hospital · USMax Planck Institute of Biochemistry · DEHarvard University · US

Funding

Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI POMEROY, SCOTT LOREN · 2016 to 2020
$5.2M
Development of a Translational Research Platform to Understand and treat Defective Protein Trafficking in Childhood-Onset Hereditary Spastic ParaplegiaK08NS123552 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI EBRAHIMI-FAKHARI, DARIUS · 2021 to 2025
$1.1M
NICHD NIH HHS U54 HD090255NINDS NIH HHS K08 NS123552
6 · The paper itself

Abstract

Unbiased phenotypic screens in patient-relevant disease models offer the potential to detect novel therapeutic targets for rare diseases. In this study, we developed a high-throughput screening assay to identify molecules that correct aberrant protein trafficking in adaptor protein complex 4 (AP-4) deficiency, a rare but prototypical form of childhood-onset hereditary spastic paraplegia, characterized by mislocalization of the autophagy protein ATG9A. Using high-content microscopy and an automated image analysis pipeline, we screened a diversity library of 28,864 small molecules and identified a lead compound,

Identifiers

PMID37398196
PMCPMC10312991
OpenAlexW4380302785

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.