Evidence map›Paper›PMID 31933239›Full record

ReviewPharmaceutical medicine2019

Analysis of Low Molecular Weight Substances and Related Processes Influencing Cellular Cholesterol Efflux.

Dmitry Y Litvinov, Eugeny V Savushkin, Alexander D Dergunov

Open access · bronzeAbstract readReview
In one paragraph

Review in Pharmaceutical medicine, 2019. 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
0.2field-weighted citation impact, top 39% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  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

3 authors at 1 institution in 1 country.

Dmitry Y LitvinovNational Research Centre for Preventive Medicine, 10, Petroverigsky Street, 101990, Moscow, Russia.
Eugeny V SavushkinNational Research Centre for Preventive Medicine, 10, Petroverigsky Street, 101990, Moscow, Russia.
Alexander D DergunovNational Research Centre for Preventive Medicine, 10, Petroverigsky Street, 101990, Moscow, Russia. dergunov@img.ras.ru.ORCID 0000-0002-0781-9890
National Research Center for Preventive Medicine · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholesterol efflux is the key process protecting the vascular system from the development of atherosclerotic lesions. Various extracellular and intracellular events affect the ability of the cell to efflux excess cholesterol. To explore the possible pathways and processes that promote or inhibit cholesterol efflux, we applied a combined cheminformatic and bioinformatic approach. We performed a comprehensive analysis of published data on the various substances influencing cholesterol efflux and found 153 low molecular weight substances that are included in the Chemical Entities of Biological Interest (ChEBI) database. Pathway enrichment was performed for substances identified within the Reactome database, and 45 substances were selected in 93 significant pathways. The most common pathways included the energy-dependent processes related to active cholesterol transport from the cell, lipoprotein metabolism and lipid transport, and signaling pathways. The activators and inhibitors of cholesterol efflux were non-uniformly distributed among the different pathways: the substances influencing 'biological oxidations' activate cholesterol efflux and the substances influencing 'Signaling by GPCR and PTK6' inhibit efflux. This analysis may be used in the search and design of efflux effectors for therapies targeting structural and functional high-density lipoprotein deficiency.

Indexed as

Anticholesteremic AgentsAtherosclerosisATP-Binding Cassette TransportersCholesterolComputational BiologyDrug DesignEnergy MetabolismHigh-Throughput Screening AssaysHumansLipid MetabolismLipoproteins, HDLMetabolic Networks and PathwaysMolecular Targeted TherapyMolecular WeightSignal TransductionAnticholesteremic AgentsATP-Binding Cassette TransportersCholesterolLipoproteins, HDL

Identifiers

PMID31933239
PMCPMC7101889
OpenAlexW2984153331

What Socratic 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 Socratic graph.