Evidence map›Paper›PMID 32075110›Full record

ArticleInternational journal of molecular sciences2020

Inhibition of Bromodomain and Extraterminal Domain (BET) Proteins by JQ1 Unravels a Novel Epigenetic Modulation to Control Lipid Homeostasis.

Claudia Tonini, Mayra Colardo, Barbara Colella, Sabrina Di Bartolomeo, Francesco Berardinelli, Giuseppina Caretti, Valentina Pallottini, Marco Segatto

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-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

21 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Lipid Biochemistry and its Role in Human Diseases.Current medicinal chemistry · 2025
    Review
  4. Article
  5. Targeting CCL2/CCR2 Signaling Overcomes MEK Inhibitor Resistance in Acute Myeloid Leukemia.Clinical cancer research : an official journal of the American Association for Cancer Research · 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

8 authors at 3 institutions in 1 country.

Claudia ToniniDepartment of Science, University of Rome "Roma Tre", Viale Marconi 446, 00146 Rome, Italy.
Mayra ColardoDepartment of Bioscience and Territory, University of Molise, Contrada Fonte Lappone, 86090 Pesche (Is), Italy.
Barbara ColellaDepartment of Bioscience and Territory, University of Molise, Contrada Fonte Lappone, 86090 Pesche (Is), Italy.
Sabrina Di BartolomeoDepartment of Bioscience and Territory, University of Molise, Contrada Fonte Lappone, 86090 Pesche (Is), Italy.
Francesco BerardinelliDepartment of Science, University of Rome "Roma Tre", Viale Marconi 446, 00146 Rome, Italy.
Giuseppina CarettiDepartment of Biosciences, University of Milan, Via Celoria 26, 20133 Milan, Italy.
Valentina PallottiniDepartment of Science, University of Rome "Roma Tre", Viale Marconi 446, 00146 Rome, Italy.
Marco SegattoDepartment of Bioscience and Territory, University of Molise, Contrada Fonte Lappone, 86090 Pesche (Is), Italy.
University of Molise · ITRoma Tre University · ITUniversity of Milan · IT

Funding

Ministero dell'Istruzione, dell'Università e della Ricerca 2015SHM58M_004
6 · The paper itself

Abstract

The homeostatic control of lipid metabolism is essential for many fundamental physiological processes. A deep understanding of its regulatory mechanisms is pivotal to unravel prospective physiopathological factors and to identify novel molecular targets that could be employed to design promising therapies in the management of lipid disorders. Here, we investigated the role of bromodomain and extraterminal domain (BET) proteins in the regulation of lipid metabolism. To reach this aim, we used a loss-of-function approach by treating HepG2 cells with JQ1, a powerful and selective BET inhibitor. The main results demonstrated that BET inhibition by JQ1 efficiently decreases intracellular lipid content, determining a significant modulation of proteins involved in lipid biosynthesis, uptake and intracellular trafficking. Importantly, the capability of BET inhibition to slow down cell proliferation is dependent on the modulation of cholesterol metabolism. Taken together, these data highlight a novel epigenetic mechanism involved in the regulation of lipid homeostasis.

Indexed as

AzepinesBromodomain Containing ProteinsCell ProliferationCholesterolEpigenesis, GeneticHep G2 CellsHumansHydroxymethylglutaryl CoA ReductasesLipid MetabolismMembrane ProteinsPhosphorylationProteinsReceptors, LDLSterol Regulatory Element Binding ProteinsTriazolesAzepinesbromodomain and extra-terminal domain protein, humanBromodomain Containing ProteinsCholesterolHMGCR protein, humanHydroxymethylglutaryl CoA Reductases(+)-JQ1 compoundMembrane ProteinsProteinsReceptors, LDLSterol Regulatory Element Binding ProteinsTMEM97 protein, humanTriazolesBET proteinscell proliferationcholesterolepigeneticsHMGCRJQ1LDLrlipid metabolismSREBPTMEM97

Identifiers

PMID32075110
PMCPMC7072965
OpenAlexW3006355107

What OpenQuestion holds

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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.