Evidence map›Paper›PMID 29229927›Full record

ArticleScientific reports2017

Activation of non-canonical WNT signaling in human visceral adipose tissue contributes to local and systemic inflammation.

María A Zuriaga, José J Fuster, Melissa G Farb, Susan MacLauchlan, Rosa Bretón-Romero, Shakun Karki, Donald T Hess, Caroline M Apovian, Naomi M Hamburg, Noyan Gokce and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

33 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
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  3. Article
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  5. Type 2 diabetes mellitus in adults: pathogenesis, prevention and therapy.Signal transduction and targeted therapy · 2024 · on this map
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  8. Prohibitions in the meta-inflammatory response: a review.Frontiers in molecular biosciences · 2024
    Review
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  15. Article
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  18. Article
  19. Perivascular Adipose Tissue Inflammation in Ischemic Heart Disease.Arteriosclerosis, thrombosis, and vascular biology · 2021
    Article
  20. 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

11 authors at 1 institution in 1 country.

María A ZuriagaMolecular Cardiology, Whitaker Cardiovascular Institute, Boston University School of Medicine, 715 Albany Street, W-611, Boston, MA, USA.
José J FusterMolecular Cardiology, Whitaker Cardiovascular Institute, Boston University School of Medicine, 715 Albany Street, W-611, Boston, MA, USA.ORCID 0000-0002-5970-629X
Melissa G FarbCardiovascular Medicine, Whitaker Cardiovascular Institute, Boston University School of Medicine, 715 Albany Street, E-7 C.H.U., Boston, MA, USA.
Susan MacLauchlanMolecular Cardiology, Whitaker Cardiovascular Institute, Boston University School of Medicine, 715 Albany Street, W-611, Boston, MA, USA.
Rosa Bretón-RomeroCardiovascular Medicine, Whitaker Cardiovascular Institute, Boston University School of Medicine, 715 Albany Street, E-7 C.H.U., Boston, MA, USA.
Shakun KarkiCardiovascular Medicine, Whitaker Cardiovascular Institute, Boston University School of Medicine, 715 Albany Street, E-7 C.H.U., Boston, MA, USA.
Donald T HessDepartment of General Surgery, Boston University School of Medicine, Boston, MA, USA.
Caroline M ApovianDepartment of Medicine, Section of Endocrinology, Diabetes and Nutrition, Boston University School of Medicine, Boston, MA, USA.
Naomi M HamburgCardiovascular Medicine, Whitaker Cardiovascular Institute, Boston University School of Medicine, 715 Albany Street, E-7 C.H.U., Boston, MA, USA.
Noyan GokceCardiovascular Medicine, Whitaker Cardiovascular Institute, Boston University School of Medicine, 715 Albany Street, E-7 C.H.U., Boston, MA, USA.
Kenneth WalshMolecular Cardiology, Whitaker Cardiovascular Institute, Boston University School of Medicine, 715 Albany Street, W-611, Boston, MA, USA. kxwalsh@bu.edu.ORCID 0000-0001-7580-2276
Boston University · US

Funding

Redox regulation in Endothelial Progenitor CellsP01HL081587 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WALSH, KENNETH · 2005 to 2015
$21.5M
Mitochondrial Dynamics and UCP2 - Endothelial Dysfunction in Human ObesityR01HL115391 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI HAMBURG, NAOMI MIRIAM · 2013 to 2017
$2.8M
Anti-Angiogenic Mechanisms in Human ObesityR01HL126141 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GOKCE, NOYAN, WALSH, KENNETH · 2015 to 2019
$2.4M
Adipose inflammation, mitochondrial function & endothelial phenotypes in obesityR01HL114675 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GOKCE, NOYAN · 2012 to 2016
$2.3M
Inflammatory Wnt signaling in ischemic myocardiumR01HL131006 · NHLBI · UNIVERSITY OF VIRGINIA · PI WALSH, KENNETH · 2016 to 2019
$2.1M
Endothelial Insulin Resistance, Inflammation and Vascular Function in DiabetesR01HL102299 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI HAMBURG, NAOMI MIRIAM · 2010 to 2014
$2.0M
Inflammatory Pathways in Aortic AneurysmsR01HL132564 · NHLBI · UNIVERSITY OF VIRGINIA · PI WALSH, KENNETH · 2016 to 2019
$1.9M
Determinants of obesity-associated insulin resistanceK23HL135394 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FARB, MELISSA G · 2017 to 2021
$895k
Myokine Control of Hepatic SteatosisR21AG052160 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WALSH, KENNETH · 2016 to 2017
$452k
NHLBI NIH HHS K23 HL135394NHLBI NIH HHS P01 HL081587NHLBI NIH HHS R01 HL102299NHLBI NIH HHS R01 HL114675NHLBI NIH HHS R01 HL115391NHLBI NIH HHS R01 HL126141NHLBI NIH HHS R01 HL131006NHLBI NIH HHS R01 HL132564NIA NIH HHS R21 AG052160
6 · The paper itself

Abstract

The accumulation of visceral adiposity is strongly associated with systemic inflammation and increased cardiometabolic risk. WNT5A, a non-canonical WNT ligand, has been shown to promote adipose tissue inflammation and insulin resistance in animal studies. Among other non-canonical pathways, WNT5A activates planar cell polarity (PCP) signaling. The current study investigated the potential contribution of non-canonical WNT5A/PCP signaling to visceral adipose tissue (VAT) inflammation and associated metabolic dysfunction in individuals with obesity. VAT and subcutaneous adipose tissue (SAT) samples obtained from subjects undergoing bariatric surgery were analyzed by qRT-PCR for expression of WNT/PCP genes. In vitro experiments were conducted with preadipocytes isolated from VAT and SAT biopsies. The expression of 23 out of 33 PCP genes was enriched in VAT compared to SAT. Strong positive expression correlations of individual PCP genes were observed in VAT. WNT5A expression in VAT, but not in SAT, correlated with indexes of JNK signaling activity, IL6, waist-to-hip ratio and hsCRP. In vitro, WNT5A promoted the expression of IL6 in human preadipocytes. In conclusion, elevated non-canonical WNT5A signaling in VAT contributes to the exacerbated IL-6 production in this depot and the low-grade systemic inflammation typically associated with visceral adiposity.

Indexed as

Gene Expression RegulationWnt Signaling PathwayAdultFemaleHumansInflammationMalePanniculitisSubcutaneous Fat

Identifiers

PMID29229927
PMCPMC5725530
OpenAlexW2772869455

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.