Evidence map›Paper›PMID 22935534›Full record

ReviewCirculation research2012

Role of phospholipid oxidation products in atherosclerosis.

Sangderk Lee, Konstantin G Birukov, Casey E Romanoski, James R Springstead, Aldons J Lusis, Judith A Berliner

Open access · bronzeAbstract readReview
In one paragraph

Review in Circulation research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

99 citing papers in PubMed, 204 citations in OpenAlex.

  1. Trial
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  7. Linking Lipidomics to Vulnerable Coronary Plaques: A PROSPECT II Substudy.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Lipid Biochemistry and its Role in Human Diseases.Current medicinal chemistry · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Review

39 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Sangderk LeeDepartment of Pathology, University of California-Los Angeles, MRL 4760, 675 Charles E. Young Dr. S., Los Angeles, CA 90095, USA.
Konstantin G Birukov
Casey E Romanoski
James R Springstead
Aldons J Lusis
Judith A Berliner
University of Chicago · US

Funding

ULTRASTRUCTURE OF THE INTIMA IN EARLY LESION FORMATIONP01HL030568 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI FOGELMAN, ALAN M · 1985 to 2019
$55.2M
Tissue Culture Biomechanical CoreP01HL058064 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LAL, RATNESHWAR · 1998 to 2012
$27.8M
Vascular Biology Training GrantT32HL069766 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LUSIS, ALDONS JAKE · 2002 to 2022
$7.4M
Control of Lung Permeability by Oxidized PhospholipidsR01HL076259 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI BIRUKOV, KONSTANTIN · 2004 to 2023
$6.8M
Molecular control of lung endothelial barrier function in ALIR01HL087823 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI BIRUKOV, KONSTANTIN · 2008 to 2020
$4.6M
ENDOTHELIAL ACTIVATION BY AN ISOPROSTANE PHOSPHOLIPIDR01HL064731 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BERLINER, JUDITH ANNE · 2000 to 2011
$3.2M
Role of MP-HBEGF-EGFR signaling for inflammatory action of oxidized phospholipidsR00HL105577 · NHLBI · UNIVERSITY OF KENTUCKY · PI LEE, SANGDERK · 2013 to 2015
$718k
Role of MP-HBEGF-EGFR signaling for inflammatory action of oxidized phospholipidsK99HL105577 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LEE, SANGDERK · 2011 to 2012
$180k
NHLBI NIH HHS 1K99HL105577NHLBI NIH HHS HL064731NHLBI NIH HHS HL30568NHLBI NIH HHS HL76259NHLBI NIH HHS HL87823NHLBI NIH HHS K99 HL105577NHLBI NIH HHS P01 HL030568NHLBI NIH HHS P01 HL058064NHLBI NIH HHS R00 HL105577NHLBI NIH HHS R01 HL064731NHLBI NIH HHS R01 HL076259NHLBI NIH HHS R01 HL087823NHLBI NIH HHS T232HL69766NHLBI NIH HHS T32 HL069766
6 · The paper itself

Abstract

There is increasing clinical evidence that phospholipid oxidation products (Ox-PL) play a role in atherosclerosis. This review focuses on the mechanisms by which Ox-PL interact with endothelial cells, monocyte/macrophages, platelets, smooth muscle cells, and HDL to promote atherogenesis. In the past few years major progress has been made in identifying these mechanisms. It has been recognized that Ox-PL promote phenotypic changes in these cell types that have long-term consequences for the vessel wall. Individual Ox-PL responsible for specific cellular effects have been identified. A model of the configuration of bioactive truncated Ox-PL within membranes has been developed that demonstrates that the oxidized fatty acid moiety protrudes into the aqueous phase, rendering it accessible for receptor recognition. Receptors and signaling pathways for individual Ox-PL species are now determined and receptor independent signaling pathways identified. The effects of Ox-PL are mediated both by gene regulation and transcription independent processes. It has now become apparent that Ox-PL affects multiple genes and pathways, some of which are proatherogenic and some are protective. However, at concentrations that are likely present in the vessel wall in atherosclerotic lesions, the effects promote atherogenesis. There have also been new insights on enzymes that metabolize Ox-PL and the significance of these enzymes for atherosclerosis. With the knowledge we now have of the regulation and effects of Ox-PL in different vascular cell types, it should be possible to design experiments to test the role of specific Ox-PL on the development of atherosclerosis.

Indexed as

Signal TransductionAtherosclerosisCytokinesEndothelial CellsHumansMacrophagesMyocytes, Smooth MuscleOxidation-ReductionPhospholipidsReceptors, Cell SurfaceCytokinesPhospholipidsReceptors, Cell Surface

Identifiers

PMID22935534
PMCPMC3563283
OpenAlexW2148989921

What OpenQuestion holds

Textmetadata
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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.