Evidence mapPaperPMID 40565243Full record

ArticleInternational journal of molecular sciences2025

Exploration of Bromodomain Proteins as Drug Targets for Niemann-Pick Type C Disease.

Martina Parente, Amélie Barthelemy, Claudia Tonini, Sara Caputo, Alessandra Sacchi, Stefano Leone, Marco Segatto, Frank W Pfrieger, Valentina Pallottini

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Martina ParenteDepartment of Science, Section Biomedical Science and Technology, University Roma Tre, Viale Marconi 446, 00146 Rome, Italy.ORCID 0000-0002-9135-567X
Amélie BarthelemyInstitut des Neurosciences Cellulaires et Intégratives, Centre National de la Recherche Scientifique, Université de Strasbourg, 8 Allée du Général Rouvillois, 67000 Strasbourg, France.
Claudia ToniniDepartment of Science, Section Biomedical Science and Technology, University Roma Tre, Viale Marconi 446, 00146 Rome, Italy.ORCID 0000-0002-9979-1142
Sara CaputoDepartment of Science, Section Biomedical Science and Technology, University Roma Tre, Viale Marconi 446, 00146 Rome, Italy.ORCID 0009-0009-9939-3767
Alessandra SacchiDepartment of Science, Section Biomedical Science and Technology, University Roma Tre, Viale Marconi 446, 00146 Rome, Italy.
Stefano LeoneDepartment of Science, Section Biomedical Science and Technology, University Roma Tre, Viale Marconi 446, 00146 Rome, Italy.ORCID 0000-0001-6339-6397
Marco SegattoDepartment of Biosciences and Territory, University of Molise, Contrada Fonte Lappone s.n.c., 86090 Pesche, Italy.ORCID 0000-0003-0465-9470
Frank W PfriegerInstitut des Neurosciences Cellulaires et Intégratives, Centre National de la Recherche Scientifique, Université de Strasbourg, 8 Allée du Général Rouvillois, 67000 Strasbourg, France.ORCID 0000-0001-7085-1431
Valentina PallottiniDepartment of Science, Section Biomedical Science and Technology, University Roma Tre, Viale Marconi 446, 00146 Rome, Italy.ORCID 0000-0003-2511-6168

Funding

Ara Parseghian Medical Research FundBILD Hilft e.V.Centre National de la Recherche Scientifique UPR3212Niemann-Pick Selbsthilfegruppe e.V.Telethon Foundation GMR23T2008Together Strong Niemann-Pick foundationUniversité de Strasbourg UPR3212
6 · The paper itself

Abstract

Defects in lysosomal cholesterol handling provoke fatal disorders presenting neurovisceral symptoms with variable onset and life spans. A prime example is Niemann-Pick type C disease (NPCD), where cholesterol export from the endosomal-lysosomal system is impaired due to variants of either NPC intracellular cholesterol transporter 1 (NPC1) or NPC intracellular cholesterol transporter 2 (NPC2). Therapeutic options for NPCD are limited to palliative care and disease-modifying drugs, and there is a need for new treatments. Here, we explored bromodomain and extra-terminal domain (BET) proteins as new drug targets for NPCD using patient-derived skin fibroblasts. Treatment with JQ1, a prototype BET protein inhibitor, raised the level of NPC1 protein, diminished lysosomal expansion and cholesterol accumulation, and induced extracellular release of lysosomal components in a dose-, time-, and patient-dependent manner. Lastly, JQ1 enhanced and reduced cholesterol accumulation induced by pharmacologic inhibition of NPC1 and of histone deacetylase (HDAC) activity, respectively. Taken together, bromodomain proteins should be further explored as therapeutic drug targets for lysosomal diseases like NPCD, and as new components regulating lysosomal function and cholesterol metabolism.

Indexed as

AzepinesNiemann-Pick Disease, Type CTriazolesBromodomain Containing ProteinsCholesterolFibroblastsHumansIntracellular Signaling Peptides and ProteinsLysosomesNiemann-Pick C1 ProteinProteinsAzepinesbromodomain and extra-terminal domain protein, humanBromodomain Containing ProteinsCholesterolIntracellular Signaling Peptides and Proteins(+)-JQ1 compoundNiemann-Pick C1 ProteinNPC1 protein, humanProteinsTriazolesBET inhibitorcholesteroldrug therapyepigenetic regulationlysosomerare disease

Identifiers

PMID40565243
PMCPMC12192928

What Socratic holds

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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 Socratic graph.