Evidence map›Paper›PMID 37123894›Full record

ArticleHeliyon2023

FGF21/FGFR1-β-KL cascade in cardiomyocytes modulates angiogenesis and inflammation under metabolic stress.

Namrita Kaur, Sanskruti Ravindra Gare, Andrea Ruiz-Velasco, Jessica M Miller, Riham R E Abouleisa, Qinghui Ou, Jiahan Shen, Handrean Soran, Tamer M A Mohamed, Wei Liu

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  8. The Cardiohepatic Axis in Metabolic Disease: Liver to Heart.JACC. Basic to translational science · 2025
    Review
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  10. Article
  11. Article
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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

10 authors at 2 institutions in 2 countries.

Namrita KaurUniversity of Manchester, Oxford Road, M13 9PT, Manchester, UK.
Sanskruti Ravindra GareUniversity of Manchester, Oxford Road, M13 9PT, Manchester, UK.
Andrea Ruiz-VelascoUniversity of Manchester, Oxford Road, M13 9PT, Manchester, UK.
Jessica M MillerInstitute of Molecular Cardiology, University of Louisville, 580 S Preston St., Louisville, KY, 40202, USA.
Riham R E AbouleisaInstitute of Molecular Cardiology, University of Louisville, 580 S Preston St., Louisville, KY, 40202, USA.
Qinghui OuInstitute of Molecular Cardiology, University of Louisville, 580 S Preston St., Louisville, KY, 40202, USA.
Jiahan ShenUniversity of Manchester, Oxford Road, M13 9PT, Manchester, UK.
Handrean SoranUniversity of Manchester, Oxford Road, M13 9PT, Manchester, UK.
Tamer M A MohamedInstitute of Molecular Cardiology, University of Louisville, 580 S Preston St., Louisville, KY, 40202, USA.
Wei LiuUniversity of Manchester, Oxford Road, M13 9PT, Manchester, UK.
University of Manchester · GBUniversity of Louisville · US

Funding

TBDP30GM127607 · NIGMS · UNIVERSITY OF LOUISVILLE · PI HILL, BRADFORD GUY · 2018 to 2022
$6.3M
Induction of Cardiomyocyte Proliferation via Transient Expression of Cell Cycle Factors as a Promising Therapy for Heart FailureR01HL147921 · NHLBI · UNIVERSITY OF LOUISVILLE · PI Tamer M A Mohamed, Jonathan Satin · 2020 to 2026
$5.3M
Defining the major signaling mechanism which controls spontaneous cardiomyocyte proliferation in the Neonatal StageR01HL178610 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI Tamer M A Mohamed · 2025 to 2026
$1.5M
Deciphering the Relationship Between Cardiomyocyte Metabolic Configuration and Cell Cycle Re-entryF32HL149140 · NHLBI · UNIVERSITY OF LOUISVILLE · PI ABOULEISA, RIHAM RAAFAT ELGHARIB · 2020 to 2023
$243k
British Heart Foundation FS/PHD/22/29307British Heart Foundation PG/19/66/34600British Heart Foundation PG/22/10904British Heart Foundation PG/22/11075NHLBI NIH HHS F32 HL149140NHLBI NIH HHS R01 HL147921NHLBI NIH HHS R01 HL178610NIGMS NIH HHS P30 GM127607
6 · The paper itself

Abstract

Diabetes is a metabolic disorder with an increased risk of developing heart failure. Inflammation and damaged vasculature are the cardinal features of diabetes-induced cardiac damage. Moreover, systemic metabolic stress triggers discordant intercellular communication, thus culminating in cardiac dysfunction. Fibroblast growth factor 21 (FGF21) is a pleiotropic hormone transducing cellular signals via fibroblast growth factor receptor 1 (FGFR1) and its co-receptor beta-klotho (β-KL). This study first demonstrated a decreased expression or activity of FGFR1 and β-KL in both human and mouse diabetic hearts. Reinforcing cardiac FGFR1 and β-KL expression can alleviate pro-inflammatory response and endothelial dysfunction upon diabetic stress. Using proteomics, novel cardiomyocyte-derived anti-inflammatory and proangiogenic factors regulated by FGFR1-β-KL signaling were identified. Although not exhaustive, this study provides a unique insight into the protective topology of the cardiac FGFR1-β-KL signaling-mediated intercellular reactions in the heart in response to metabolic stress.

Indexed as

AngiogenesisDiabetic cardiomyopathyInflammationIntercellular communicationMetabolic stress

Identifiers

PMID37123894
PMCPMC10133673
OpenAlexW4361275521

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.