Evidence map›Paper›PMID 38022905›Full record

ReviewJournal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques2023

Current investigations for liver fibrosis treatment: between repurposing the FDA-approved drugs and the other emerging approaches.

Omima S Mohammed, Hany G Attia, Bassim M S A Mohamed, Marawan A Elbaset, Hany M Fayed

Open access · diamondAbstract readReview
In one paragraph

Review in Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

33 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Review
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  6. Animal models accurately representing acute liver failure (Review).International journal of molecular medicine · 2026
    Review
  7. Review
  8. Article
  9. Article
  10. Bicuculline fromComputational and structural biotechnology journal · 2026
    Article
  11. Article
  12. Article
  13. Article
  14. Exploring Cirrhosis: Insights into Advances in Therapeutic Strategies.International journal of molecular sciences · 2025
    Review
  15. Article
  16. Anti-Fibrotic Effect of Oleamide Identified from theInternational journal of molecular sciences · 2025
    Article
  17. Targeting TGF-β: a promising strategy for cancer therapy.Medical oncology (Northwood, London, England) · 2025
    Review
  18. Article
  19. 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

5 authors at 2 institutions in 2 countries.

Omima S MohammedDepartment of Microbiology, College of Medicine, Najran University, Najran, Saudi Arabia.
Hany G AttiaDepartment of Pharmacognosy, College of Pharmacy, Najran University, Najran, Saudi Arabia.
Bassim M S A MohamedDepartment of Pharmacology, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt.
Marawan A ElbasetDepartment of Pharmacology, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt.
Hany M FayedDepartment of Pharmacology, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt.
National Research Centre · EGNajran University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long-term liver injuries lead to hepatic fibrosis, often progressing into cirrhosis, liver failure, portal hypertension, and hepatocellular carcinoma. There is currently no effective therapy available for liver fibrosis. Thus, continuous investigations for anti-fibrotic therapy are ongoing. The main theme of anti-fibrotic investigation during recent years is the rationale-based selection of treatment molecules according to the current understanding of the pathology of the disease. The research efforts are mainly toward repurposing current FDA-approved drugs targeting etiological molecular factors involved in developing liver fibrosis. In parallel, investigations also focus on experimental small molecules with evidence to hinder or reverse the fibrosis. Natural compounds, immunological, and genetic approaches have shown significant encouraging effects. This review summarizes the efficacy and safety of current under-investigation antifibrosis medications targeting various molecular targets, as well as the properties of antifibrosis medications, mainly in phase II and III clinical trials.

Indexed as

Drug RepositioningLiver CirrhosisHumansLiveranti-fibrotic agentsHSCsliver fibrosispharmacotherapytherapeutic targets

Identifiers

PMID38022905
PMCPMC10662312
OpenAlexW4388461418

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.