Evidence map›Paper›PMID 34746149›Full record

ArticleFrontiers in cell and developmental biology2021

Fibroblast Growth Factor 21 Augments Autophagy and Reduces Apoptosis in Damaged Liver to Improve Tissue Regeneration in Zebrafish.

Weidong Qiang, Tianzhu Shen, Muhammad Noman, Jinnan Guo, Zhongqian Jin, Danfeng Lin, Jiaxuan Pan, Huiqiang Lu, Xiaokun Li, Fanghua Gong

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Using different zebrafish models to explore liver regeneration.Frontiers in cell and developmental biology · 2024
    Review
  12. Article
  13. Article
  14. mTORC1 signaling pathway regulates tooth repair.International journal of oral science · 2023
    Article
  15. Review
  16. Review
  17. Frontiers in endocrinology · 2021
    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

10 authors at 3 institutions in 1 country.

Weidong QiangCollege of Life Sciences, Jilin Agricultural University, Changchun, China.
Tianzhu ShenSchool of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Muhammad NomanCollege of Life Sciences, Jilin Agricultural University, Changchun, China.
Jinnan GuoCollege of Life Sciences, Jilin Agricultural University, Changchun, China.
Zhongqian JinSchool of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Danfeng LinSchool of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Jiaxuan PanSchool of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Huiqiang LuCenter for Drug Screening and Research, College of Geography and Environmental Engineering, Gannan Normal University, Ganzhou, China.
Xiaokun LiCollege of Life Sciences, Jilin Agricultural University, Changchun, China.
Fanghua GongSchool of Pharmacy, Wenzhou Medical University, Wenzhou, China.
Wenzhou Medical University · CNJilin Agricultural University · CNJinggangshan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regeneration of a part of the diseased liver after surgical resection is mainly achieved by the proliferation of the remaining healthy liver cells. However, in case of extreme loss of liver cells or in the final stages of chronic liver disease, most liver cells are depleted or lose their ability to proliferate. Therefore, to foster liver regeneration, it is of great clinical and scientific significance to improve the survival and proliferation ability of residual hepatocytes. In this study, we conducted experiments on a zebrafish model of targeted ablation of liver cells to clarify the role of fibroblast growth factor 21 (FGF21). We found that FGF21 increased the regeneration area of the damaged liver and improved the survival rate of damaged liver cells by inhibiting cell apoptosis and reducing oxidative stress. Our results also showed that administration of FGF21 upregulated autophagy, and the beneficial effects of FGF21 were reversed by the well-known autophagy inhibitor chloroquine (CQ), indicating that FGF21-activated autophagy played a central role in the treatment. We further showed that the enhancement of autophagy induced by FGF21 was due to the activation of the AMPK-mTOR signaling pathway. Taken together, these data provide new evidence that FGF21 is an effective autophagy regulator that can significantly improve the survival of damaged livers.

Indexed as

autophagydamaged liverFGF21regenerationzebrafish

Identifiers

PMID34746149
PMCPMC8570170
OpenAlexW3208846809

What OpenQuestion holds

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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.