Evidence map›Paper›PMID 29253870›Full record

ArticlePloS one2017

Downregulation of monocytic differentiation via modulation of CD147 by 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors.

Manda V Sasidhar, Sai Krishnaveni Chevooru, Oliver Eickelberg, Hans-Peter Hartung, Oliver Neuhaus

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. CD147/Basigin: From Integrative Molecular Hub to Translational Therapeutic Target.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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 4 institutions in 3 countries.

Manda V SasidharDepartment of Neurology, Heinrich Heine University, Düsseldorf, Germany.
Sai Krishnaveni ChevooruDepartment of Internal Medicine II, Molecular Biology and Medicine of the Lung, Justus Liebig University, Giessen, Germany.
Oliver EickelbergDepartment of Internal Medicine II, Molecular Biology and Medicine of the Lung, Justus Liebig University, Giessen, Germany.
Hans-Peter HartungDepartment of Neurology, Heinrich Heine University, Düsseldorf, Germany.
Oliver NeuhausDepartment of Neurology, Heinrich Heine University, Düsseldorf, Germany.ORCID http://orcid.org/0000-0002-5496-2243
Justus-Liebig-Universität Gießen · DEAlbstadt-Sigmaringen University · DEApollo Hospitals · INHeinrich Heine University Düsseldorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD147 is an activation induced glycoprotein that promotes the secretion and activation of matrix metalloproteinases (MMPs) and is upregulated during the differentiation of macrophages. Interestingly, some of the molecular functions of CD147 rely on its glycosylation status: the highly glycosylated forms of CD147 induce MMPs whereas the lowly glycosylated forms inhibit MMP activation. Statins are hydroxy-methylglutaryl coenzyme A reductase inhibitors that block the synthesis of mevalonate, thereby inhibiting all mevalonate-dependent pathways, including isoprenylation, N-glycosylation and cholesterol synthesis. In this study, we investigated the role of statins in the inhibition of macrophage differentiation and the associated process of MMP secretion through modulation of CD147. We observed that differentiation of the human monocytic cell line THP-1 to a macrophage phenotype led to upregulation of CD147 and CD14 and that this effect was inhibited by statins. At the molecular level, statins altered CD147 expression, structure and function by inhibiting isoprenylation and N-glycosylation. In addition, statins induced a shift of CD147 from its highly glycosylated form to its lowly glycosylated form. This shift in N-glycosylation status was accompanied by a decrease in the production and functional activity of MMP-2 and MMP-9. In conclusion, these findings describe a novel molecular mechanism of immune regulation by statins, making them interesting candidates for autoimmune disease therapy.

Indexed as

Autoimmune DiseasesBasiginBiotinylationCell DifferentiationCell MembraneGlycosylationHumansHydroxymethylglutaryl-CoA Reductase InhibitorsImmune SystemLipopolysaccharide ReceptorsMacrophagesMatrix Metalloproteinase 2Matrix Metalloproteinase 9MonocytesPermeabilityPhenotypeBasiginBSG protein, humanHydroxymethylglutaryl-CoA Reductase InhibitorsLipopolysaccharide ReceptorsMatrix Metalloproteinase 2Matrix Metalloproteinase 9MMP2 protein, humanMMP9 protein, human

Identifiers

PMID29253870
PMCPMC5734787
OpenAlexW2777724025

What OpenQuestion 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 OpenQuestion graph.