Evidence map›Paper›PMID 29699061›Full record

ArticleGut and liver2018

Expression of Fibroblast Growth Factor 21 and β-Klotho Regulates Hepatic Fibrosis through the Nuclear Factor-κB and c-Jun N-Terminal Kinase Pathways.

Kyong Joo Lee, Yoon Ok Jang, Seung-Kuy Cha, Moon Young Kim, Kyu-Sang Park, Young Woo Eom, Soon Koo Baik

Open access · diamondAbstract read
In one paragraph

Article in Gut and liver, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.0field-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

27 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. c-Jun N-terminal kinase signaling in aging.Frontiers in aging neuroscience · 2024
    Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Drug Discovery in Liver Disease Using Kinome Profiling.International journal of molecular sciences · 2021
    Review
  18. Review
  19. Article
  20. Article
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

7 authors at 1 institution in 1 country.

Kyong Joo LeeDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Yoon Ok JangDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Seung-Kuy ChaDepartment of Physiology, Yonsei University Wonju College of Medicine, Wonju, Korea.
Moon Young KimDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Kyu-Sang ParkDepartment of Physiology, Yonsei University Wonju College of Medicine, Wonju, Korea.
Young Woo EomCell Therapy and Tissue Engineering Center, Yonsei University Wonju College of Medicine, Wonju, Korea.
Soon Koo BaikDepartment of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
Yonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aims: Fibroblast growth factor (FGF) 21 is associated with hepatic inflammation and fibrosis. However, little is known regarding the effects of inflammation and fibrosis on the β-Klotho and FGF21 pathway in the liver. Methods: Enrolled patients had biopsy-confirmed viral or alcoholic hepatitis. FGF19, FGF21 and β-Klotho levels were evaluated using enzyme-linked immunosorbent assay, real-time polymerase chain reaction, and Western blotting. Furthermore, we explored the underlying mechanisms for this process by evaluating nuclear factor-κB (NF-κB) and c-Jun N-terminal kinase (JNK) pathway involvement in Huh-7 cells. Results: We observed that the FGF19 and FGF21 serum and mRNA levels in the biopsied liver tissue gradually increased and were correlated with fibrosis stage. Inflammatory markers (interleukin 1β [IL-1β], IL-6, and tumor necrosis factor-α) were positively correlated, while β-Klotho expression was negatively correlated with the degree of fibrosis. In Huh-7 cells, IL-1β increased FGF21 levels and decreased β-Klotho levels. NF-κB and JNK inhibitors abolished the effect of IL-1β on both FGF21 and β-Klotho expression. FGF21 protected IL-1β-induced growth retardation in Huh-7 cells. Conclusions: These results indicate that the inflammatory response during fibrogenesis increases FGF21 levels and suppresses β-Klotho via the NF-κB and JNK pathway. In addition, FGF21 likely protects hepatocytes from hepatic inflammation and fibrosis.

Indexed as

AdolescentAdultAgedFemaleFibroblast Growth FactorsHepatitis, AlcoholicHepatitis, Viral, HumanHepatocytesHumansJNK Mitogen-Activated Protein KinasesKlotho ProteinsLiverLiver CirrhosisMaleMembrane ProteinsMiddle Agedfibroblast growth factor 21Fibroblast Growth FactorsJNK Mitogen-Activated Protein KinasesKLB protein, humanKlotho ProteinsMembrane ProteinsNF-kappa BFibroblast growth factor 21Interleukin-1betaJNKNF-kappa Bβ-Klotho

Identifiers

PMID29699061
PMCPMC6027831
OpenAlexW2801424129

What OpenQuestion holds

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LicenceCC BY-NC
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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.