Evidence map›Paper›PMID 30464200›Full record

ArticleScientific reports2018

Suppression of Hepatic Bile Acid Synthesis by a non-tumorigenic FGF19 analogue Protects Mice from Fibrosis and Hepatocarcinogenesis.

Raffaella Maria Gadaleta, Natasha Scialpi, Claudia Peres, Marica Cariello, Brian Ko, Jian Luo, Emanuele Porru, Aldo Roda, Carlo Sabbà, Antonio Moschetta

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 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 12% 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, 52 citations in OpenAlex.

  1. Review
  2. The Role of Gut Microbiota in Liver Regeneration After Partial Hepatectomy: New Evidence From Animal and Human Studies.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. [Bile acid metabolism and the occurrence and development of primary liver cancer].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2025
    Review
  7. Review
  8. Frontiers in pharmacology · 2024
    Review
  9. Review
  10. Article
  11. Engineered FGF19BMC biotechnology · 2023
    Article
  12. Review
  13. Review
  14. Article
  15. Pleiotropic roles of FXR in liver and colorectal cancers.Molecular and cellular endocrinology · 2022
    Article
  16. Review
  17. Review
  18. Review
  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

10 authors at 5 institutions in 2 countries.

Raffaella Maria GadaletaDepartment of Interdisciplinary Medicine, "Aldo Moro" University of Bari, Bari, Italy.ORCID http://orcid.org/0000-0003-4951-9543
Natasha ScialpiDepartment of Interdisciplinary Medicine, "Aldo Moro" University of Bari, Bari, Italy.
Claudia PeresDepartment of Interdisciplinary Medicine, "Aldo Moro" University of Bari, Bari, Italy.
Marica CarielloDepartment of Interdisciplinary Medicine, "Aldo Moro" University of Bari, Bari, Italy.
Brian KoNGM Biopharmaceuticals, South San Francisco, CA, USA.
Jian LuoNGM Biopharmaceuticals, South San Francisco, CA, USA.
Emanuele PorruDepartment of Chemistry "Giacomo Ciamician", Alma Mater Studiorum, University of Bologna, Bologna, Italy.
Aldo RodaDepartment of Chemistry "Giacomo Ciamician", Alma Mater Studiorum, University of Bologna, Bologna, Italy.
Carlo SabbàDepartment of Interdisciplinary Medicine, "Aldo Moro" University of Bari, Bari, Italy.
Antonio MoschettaDepartment of Interdisciplinary Medicine, "Aldo Moro" University of Bari, Bari, Italy. antonio.moschetta@uniba.it.
Istituto Nazionale Biostrutture e Biosistemi · ITNGM Biopharmaceuticals (United States) · USUniversity of Bari Aldo Moro · ITUniversity of Bologna · ITIstituto Tumori Bari · IT

Funding

Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) IG 18987
6 · The paper itself

Abstract

Critical regulation of bile acid (BA) pool size and composition occurs via an intensive molecular crosstalk between the liver and gut, orchestrated by the combined actions of the nuclear Farnesoid X receptor (FXR) and the enterokine fibroblast growth factor 19 (FGF19) with the final aim of reducing hepatic BA synthesis in a negative feedback fashion. Disruption of BA homeostasis with increased hepatic BA toxic levels leads to higher incidence of hepatocellular carcinoma (HCC). While native FGF19 has anti-cholestatic and anti-fibrotic activity in the liver, it retains peculiar pro-tumorigenic actions. Thus, novel analogues have been generated to avoid tumorigenic capacity and maintain BA metabolic action. Here, using BA related Abcb4

Indexed as

AnimalsBile Acids and SaltsBiological ProductsCarcinoma, HepatocellularDisease Models, AnimalFibroblast Growth FactorsGastrointestinal AgentsLiver CirrhosisMiceMice, KnockoutMutant ProteinsTreatment OutcomeBile Acids and SaltsBiological Productsfibroblast growth factor 15, mouseFibroblast Growth FactorsGastrointestinal AgentsMutant Proteins

Identifiers

PMID30464200
PMCPMC6249240
OpenAlexW2901310750

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.