Evidence map›Paper›PMID 24023685›Full record

ArticlePloS one2013

Bevacizumab attenuates hepatic fibrosis in rats by inhibiting activation of hepatic stellate cells.

Yangqing Huang, Helin Feng, Tong Kan, Bin Huang, Minfeng Zhang, Yesheng Li, Changying Shi, Mengchao Wu, Yunquan Luo, Jiamei Yang and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

26 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Hepatic inflammatory responses in liver fibrosis.Nature reviews. Gastroenterology & hepatology · 2023
    Review
  10. [An update of understanding of the hepatic vascular system and new research strategies].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    Review
  11. Article
  12. The roles and mechanisms of hypoxia in liver fibrosis.Journal of translational medicine · 2021
    Review
  13. Role of Angiogenesis in the Pathogenesis of NAFLD.Journal of clinical medicine · 2021
    Review
  14. Article
  15. Article
  16. Review
  17. Therapeutic molecular targets of SSc-ILD.Journal of scleroderma and related disorders · 2020
    Article
  18. Review
  19. Hepatic Stellate Cells and Hepatocarcinogenesis.Frontiers in cell and developmental biology · 2020
    Review
  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

11 authors at 4 institutions in 1 country.

Yangqing HuangDepartment of Special Treatment, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, China ; Department of Hepatobiliary Surgery, Shuguang Hospital, Shanghai, China.
Helin Feng
Tong Kan
Bin Huang
Minfeng Zhang
Yesheng Li
Changying Shi
Mengchao Wu
Yunquan Luo
Jiamei Yang
Feng Xu
Eastern Hepatobiliary Surgery Hospital · CNSecond Military Medical University · CNFourth Hospital of Hebei Medical University · CNShanghai University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiogenesis is a fundamental part of the response to tissue injury, which is involved in the development of hepatic fibrosis. Vascular endothelial growth factor plays an important role in angiogenesis. The expression of VEGF is increased during hepatic fibrogenesis and correlates with the micro-vessel density. In this study, we investigated the effects of bevacizumab, an anti-angiogenetic drug, on the formation of hepatic fibrosis. We found that bevacizumab could attenuate the development of hepatic fibrosis and contribute to the protection of liver function. Bevacizumab was also found to downregulate the expression α-SMA and TGF-β1, which have been reported to be profibrogenic genes in vivo. We also observed that the expression of VEGF increased significantly during the development of hepatic fibrosis and CCl4 was found to induce hepatocytes to secrete VEGF, which led to the activation and proliferation of HSCs. Bevacizumab was also found to block the effects of the hepatocytes on the activation and proliferation of HSCs. Our results suggest that bevacizumab might alleviate liver fibrosis by blocking the effect of VEGF on HSCs. Bevacizumab might be suitable as a potential agent for hepatic fibrosis therapy.

Indexed as

AnimalsAntibodies, Monoclonal, HumanizedBevacizumabCarbon TetrachlorideCell ProliferationCulture Media, ConditionedDown-RegulationHepatic Stellate CellsHepatocytesLiver CirrhosisLiver Function TestsMaleRatsRats, Sprague-DawleyUp-RegulationVascular Endothelial Growth Factor AAntibodies, Monoclonal, HumanizedBevacizumabCarbon TetrachlorideCulture Media, ConditionedVascular Endothelial Growth Factor A

Identifiers

PMID24023685
PMCPMC3758295
OpenAlexW1981175286

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.