Evidence map›Paper›PMID 31382500›Full record

ReviewInternational journal of molecular sciences2019

Revisiting the Role of LXRs in PUFA Metabolism and Phospholipid Homeostasis.

Antoine Jalil, Thibaut Bourgeois, Louise Ménégaut, Laurent Lagrost, Charles Thomas, David Masson

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Total alkaloids fromFrontiers in pharmacology · 2025
    Article
  10. Article
  11. LXR agonism for CNS diseases: promises and challenges.Journal of neuroinflammation · 2024
    Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. ApoE Lipidation as a Therapeutic Target in Alzheimer's Disease.International journal of molecular sciences · 2020
    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

6 authors at 1 institution in 1 country.

Antoine JalilUniversité Bourgogne Franche-Comté, LNC UMR1231, F-21000 Dijon, France.
Thibaut BourgeoisUniversité Bourgogne Franche-Comté, LNC UMR1231, F-21000 Dijon, France.
Louise MénégautUniversité Bourgogne Franche-Comté, LNC UMR1231, F-21000 Dijon, France.
Laurent LagrostUniversité Bourgogne Franche-Comté, LNC UMR1231, F-21000 Dijon, France.
Charles ThomasUniversité Bourgogne Franche-Comté, LNC UMR1231, F-21000 Dijon, France.ORCID 0000-0001-9998-6698
David MassonUniversité Bourgogne Franche-Comté, LNC UMR1231, F-21000 Dijon, France. david.masson@chu-dijon.fr.
Inserm · FR

Funding

Agence Nationale de la Recherche ANR-11-LABX-0021Agence Nationale de la Recherche ANR-15-IDEX-0003
6 · The paper itself

Abstract

Liver X receptors (LXRs) play a pivotal role in fatty acid (FA) metabolism. So far, the lipogenic consequences of in vivo LXR activation, as characterized by a major hepatic steatosis, has constituted a limitation to the clinical development of pharmacological LXR agonists. However, recent studies provided a different perspective. Beyond the quantitative accumulation of FA, it appears that LXRs induce qualitative changes in the FA profile and in the distribution of FAs among cellular lipid species. Thus, LXRs activate the production of polyunsaturated fatty acids (PUFAs) and their distribution into phospholipids via the control of FA desaturases, FA elongases, lysophosphatidylcholine acyltransferase (LPCAT3), and phospholipid transfer protein (PLTP). Therefore, LXRs control, in a dynamic manner, the PUFA composition and the physicochemical properties of cell membranes as well as the release of PUFA-derived lipid mediators. Recent studies suggest that modulation of PUFA and phospholipid metabolism by LXRs are involved in the control of lipogenesis and lipoprotein secretion by the liver. In myeloid cells, the interplay between LXR and PUFA metabolism affects the inflammatory response. Revisiting the complex role of LXRs in FA metabolism may open new opportunities for the development of LXR modulators in the field of cardiometabolic diseases.

Indexed as

AnimalsFatty Acids, UnsaturatedHomeostasisHumansInflammationLipogenesisLipoproteins, VLDLLiverLiver X ReceptorsPhospholipidsFatty Acids, UnsaturatedLipoproteins, VLDLLiver X ReceptorsPhospholipidsinflammationlipogenesisliver X receptorsphospholipidspolyunsaturated fatty acids

Identifiers

PMID31382500
PMCPMC6696407
OpenAlexW2964774219

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.