Evidence map›Paper›PMID 26592976›Full record

ArticleNature communications2015

Saturated fatty acids regulate retinoic acid signalling and suppress tumorigenesis by targeting fatty acid-binding protein 5.

Liraz Levi, Zeneng Wang, Mary Kathryn Doud, Stanley L Hazen, Noa Noy

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 7% 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

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 107 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Single-Cell Pan-Cancer Atlas Reveals GPR171 as a Candidate Marker of CD8International journal of molecular sciences · 2026
    Article
  4. Review
  5. Epithelial sensing of vitamin A shapes intestinal antimicrobial defense.bioRxiv : the preprint server for biology · 2026
    Article
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1 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

5 authors at 1 institution in 1 country.

Liraz LeviDepartment of Cellular &Molecular Medicine, Cleveland Clinic, 9500 Euclid Avenue, NC-10, Cleveland, Ohio 44195, USA.
Zeneng WangDepartment of Cellular &Molecular Medicine, Cleveland Clinic, 9500 Euclid Avenue, NC-10, Cleveland, Ohio 44195, USA.
Mary Kathryn DoudDepartment of Cellular &Molecular Medicine, Cleveland Clinic, 9500 Euclid Avenue, NC-10, Cleveland, Ohio 44195, USA.
Stanley L HazenDepartment of Cellular &Molecular Medicine, Cleveland Clinic, 9500 Euclid Avenue, NC-10, Cleveland, Ohio 44195, USA.
Noa NoyDepartment of Cellular &Molecular Medicine, Cleveland Clinic, 9500 Euclid Avenue, NC-10, Cleveland, Ohio 44195, USA.
Cleveland Clinic · US

Funding

Structural Determinants Of Ceruloplasmin Inflammatory ActivityP01HL076491 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI PLOW, EDWARD FRANKLIN · 2004 to 2019
$27.3M
FUNCTIONS OF INTRACELLULAR LIPID-BINDING PROTEINSR01DK060684 · NIDDK · CORNELL UNIVERSITY ITHACA · PI BROWN, JONATHAN MARK · 2002 to 2015
$4.3M
NHLBI NIH HHS HL076491NHLBI NIH HHS P01 HL076491NIDDK NIH HHS DK060684NIDDK NIH HHS R01 DK060684
6 · The paper itself

Abstract

Long chain fatty acids (LCFA) serve as energy sources, components of cell membranes and precursors for signalling molecules. Here we show that these biological compounds also regulate gene expression and that they do so by controlling the transcriptional activities of the retinoic acid (RA)-activated nuclear receptors RAR and PPARβ/δ. The data indicate that these activities of LCFA are mediated by FABP5, which delivers ligands from the cytosol to nuclear PPARβ/δ. Both saturated and unsaturated LCFA (SLCFA, ULCFA) bind to FABP5, thereby displacing RA and diverting it to RAR. However, while SLCFA inhibit, ULCFA activate the FABP5/PPARβ/δ pathway. We show further that, by concomitantly promoting the activation of RAR and inhibiting the activation of PPARβ/δ, SLCFA suppress the oncogenic properties of FABP5-expressing carcinoma cells in cultured cells and in vivo. The observations suggest that compounds that inhibit FABP5 may constitute a new class of drugs for therapy of certain types of cancer.

Indexed as

Signal TransductionCarcinogenesisCell Line, TumorDown-RegulationFatty Acid-Binding ProteinsFatty AcidsHumansPPAR-betaPPAR deltaReceptors, Retinoic AcidTretinoinFABP5 protein, humanFatty Acid-Binding ProteinsFatty AcidsPPAR-betaPPAR deltaReceptors, Retinoic AcidTretinoin

Identifiers

PMID26592976
PMCPMC4662070
OpenAlexW2172674054

What OpenQuestion holds

Textmetadata
LicenceTDM
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.