Evidence map›Paper›PMID 25032960›Full record

ArticlePloS one2014

Pharmacologic inhibition of sphingomyelin synthase (SMS) activity reduces apolipoprotein-B secretion from hepatocytes and attenuates endotoxin-mediated macrophage inflammation.

Bin Lou, Jibin Dong, Yali Li, Tingbo Ding, Tingting Bi, Yue Li, Xiaodong Deng, Deyong Ye, Xian-Cheng Jiang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Sphingomyelin Synthase Family and Phospholipase Cs.Advances in experimental medicine and biology · 2022
    Article
  6. Article
  7. Effect of liver total sphingomyelin synthase deficiency on plasma lipid metabolism.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2021
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
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 at 2 institutions in 2 countries.

Bin LouSchool of Pharmacy Fudan University, Shanghai, China.
Jibin DongSchool of Pharmacy Fudan University, Shanghai, China.
Yali LiSchool of Pharmacy Fudan University, Shanghai, China.
Tingbo DingSchool of Pharmacy Fudan University, Shanghai, China.
Tingting BiSchool of Pharmacy Fudan University, Shanghai, China.
Yue LiSchool of Pharmacy Fudan University, Shanghai, China.
Xiaodong DengSchool of Pharmacy Fudan University, Shanghai, China.
Deyong YeSchool of Pharmacy Fudan University, Shanghai, China.
Xian-Cheng JiangSchool of Pharmacy Fudan University, Shanghai, China; Department of Cell Biology, SUNY Downstate Medical Center, Brooklyn, New York United States of America.
Fudan University · CNSUNY Downstate Health Sciences University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sphingomyelin synthase (SMS) plays an important role in plasma atherogenic lipoprotein metabolism, inflammation, and the development of atherosclerosis. To understand whether the impaired apoB secretion and inflammation response is a direct result from lack of SMS activity, in this study, we prepared a series of compounds that inhibit SMS activity. Further, we characterized Dy105, the most potent inhibitor. We found that Dy105 treatment significantly reduces SM levels in SM-rich microdomain on cell membranes. Moreover, we found that SMS inhibition reduces apoB secretion in a human hepatoma cell line and reduces the activation of NFκB and p38, a MAP kinase, in bone marrow derived macrophages. These studies provided further evidence that SMS activity regulates atherogenic lipoprotein metabolism and inflammatory responses. Pharmacologic inhibition of SMS may be a new therapy for atherosclerosis by reducing apoB secretion, and reducing inflammation.

Indexed as

AcetonitrilesAnimalsApolipoproteins BAtherosclerosisBone Marrow CellsCell Line, TumorCell MembraneEndotoxinsEnzyme ActivationHepatocytesHumansInflammationMacrophagesMaleMiceMice, Inbred C57BLAcetonitrilesApolipoproteins BEndotoxinsNF-kappa Bp38 Mitogen-Activated Protein Kinasesphosphatidylcholine-ceramide phosphocholine transferaseSphingomyelinsTransferases (Other Substituted Phosphate Groups)

Identifiers

PMID25032960
PMCPMC4102531
OpenAlexW2084918839

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.