Evidence map›Paper›PMID 30996006›Full record

ArticleThe Journal of biological chemistry2019

Phosphorylation of hepatic farnesoid X receptor by FGF19 signaling-activated Src maintains cholesterol levels and protects from atherosclerosis.

Sangwon Byun, Hyunkyung Jung, Jinjing Chen, Young-Chae Kim, Dong-Hyun Kim, Bo Kong, Grace Guo, Byron Kemper, Jongsook Kim Kemper

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  5. FGF-based drug discovery: advances and challenges.Nature reviews. Drug discovery · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Review
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  12. Article
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  16. Article
  17. Role of FXR in Renal Physiology and Kidney Diseases.International journal of molecular sciences · 2023
    Review
  18. Review
  19. Review
  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

9 authors at 2 institutions in 1 country.

Sangwon ByunFrom the Department of Molecular and Integrative Physiology, University of Illinois, Urbana, Illinois 61801 and.
Hyunkyung JungFrom the Department of Molecular and Integrative Physiology, University of Illinois, Urbana, Illinois 61801 and.
Jinjing ChenFrom the Department of Molecular and Integrative Physiology, University of Illinois, Urbana, Illinois 61801 and.
Young-Chae KimFrom the Department of Molecular and Integrative Physiology, University of Illinois, Urbana, Illinois 61801 and.
Dong-Hyun KimFrom the Department of Molecular and Integrative Physiology, University of Illinois, Urbana, Illinois 61801 and.ORCID 0000-0001-8995-9426
Bo Kongthe Department of Pharmacology and Toxicology, Ernest Mario School of Pharmacy, Rutgers University, Piscataway, New Jersey 08854.
Grace Guothe Department of Pharmacology and Toxicology, Ernest Mario School of Pharmacy, Rutgers University, Piscataway, New Jersey 08854.
Byron KemperFrom the Department of Molecular and Integrative Physiology, University of Illinois, Urbana, Illinois 61801 and.
Jongsook Kim KemperFrom the Department of Molecular and Integrative Physiology, University of Illinois, Urbana, Illinois 61801 and jongsook@illinois.edu.
University of Illinois Urbana-Champaign · USRutgers, The State University of New Jersey · US

Funding

Regulation of Cholesterol Catabolism by Bile AcidsR01DK062777 · NIDDK · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI KEMPER, JONGSOOK KIM · 2003 to 2021
$5.8M
Coordination of gut-liver bile acid signaling by FXRR01DK095842 · NIDDK · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI KEMPER, JONGSOOK KIM · 2012 to 2021
$3.0M
Regulation of cholesterol catabolism by bile acidsR56DK062777 · NIDDK · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI KEMPER, JONGSOOK KIM · 2008 to 2008
$192k
NIDDK NIH HHS R01 DK062777NIDDK NIH HHS R01 DK095842NIDDK NIH HHS R56 DK062777
6 · The paper itself

Abstract

The bile acid (BA) nuclear receptor, farnesoid X receptor (FXR/NR1H4), maintains metabolic homeostasis by transcriptional control of numerous genes, including an intestinal hormone, fibroblast growth factor-19 (FGF19; FGF15 in mice). Besides activation by BAs, the gene-regulatory function of FXR is also modulated by hormone or nutrient signaling-induced post-translational modifications. Recently, phosphorylation at Tyr-67 by the FGF15/19 signaling-activated nonreceptor tyrosine kinase Src was shown to be important for FXR function in BA homeostasis. Here, we examined the role of this FXR phosphorylation in cholesterol regulation. In both hepatic FXR-knockout and FXR-knockdown mice, reconstitution of FXR expression up-regulated cholesterol transport genes for its biliary excretion, including scavenger receptor class B member 1 (

Indexed as

AnimalsAtherosclerosisATP Binding Cassette Transporter, Subfamily G, Member 8Bile Acids and SaltsCholesterolDown-RegulationFibroblast Growth FactorsHepatocytesLipoproteinsMiceMice, Inbred C57BLMice, KnockoutMutagenesis, Site-DirectedPhosphorylationReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearABCG8 protein, mouseATP Binding Cassette Transporter, Subfamily G, Member 8Bile Acids and SaltsCholesterolfibroblast growth factor 15, mouseFibroblast Growth FactorsLipoproteinsReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearRNA, Small InterferingScarb1 protein, mouseScavenger Receptors, Class Bsrc-Family KinasesAbcg8atherosclerosisATP-binding cassette subfamily G member 5 (Abcg5)bile acidbiliary excretioncholesterol regulationFGF15hypercholesterolemiametabolic homeostasisnuclear receptorpost-translational modification (PTM)reverse cholesterol transportscavenger receptor class B member 1 (Scarb1)

Identifiers

PMID30996006
PMCPMC6552419
OpenAlexW2938849305

What OpenQuestion holds

Textmetadata
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.