Evidence map›Paper›PMID 9742123›Full record

ArticleMolecular and cellular biology1998

FGF-18, a novel member of the fibroblast growth factor family, stimulates hepatic and intestinal proliferation.

M C Hu, W R Qiu, Y P Wang, D Hill, B D Ring, S Scully, B Bolon, M DeRose, R Luethy, W S Simonet and 2 more

Abstract read
In one paragraph

Article in Molecular and cellular biology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 151 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Role of FGF-18 in Bone Regeneration.Journal of functional biomaterials · 2023
    Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Generation and validation of novel conditional flox and inducible Cre alleles targeting fibroblast growth factor 18 (Fgf18).Developmental dynamics : an official publication of the American Association of Anatomists · 2019
    Article
  17. Article
  18. Article
  19. Article
  20. Regulation of Bone Metabolism.Reports of biochemistry & molecular biology · 2017
    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

12 authors at 2 institutions in 2 countries.

M C HuDepartments of Cell Biology, Amgen, Inc., Thousand Oaks, California 91320, USA. mhu@amgen.com
W R Qiu
Y P Wang
D Hill
B D Ring
S Scully
B Bolon
M DeRose
R Luethy
W S Simonet
T Arakawa
D M Danilenko
Institute of Cell Biology · UAAmgen (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The fibroblast growth factors (FGFs) play key roles in controlling tissue growth, morphogenesis, and repair in animals. We have cloned a novel member of the FGF family, designated FGF-18, that is expressed primarily in the lungs and kidneys and at lower levels in the heart, testes, spleen, skeletal muscle, and brain. Sequence comparison indicates that FGF-18 is highly conserved between humans and mice and is most homologous to FGF-8 among the FGF family members. FGF-18 has a typical signal sequence and was glycosylated and secreted when it was transfected into 293-EBNA cells. Recombinant murine FGF-18 protein (rMuFGF-18) stimulated proliferation in the fibroblast cell line NIH 3T3 in vitro in a heparan sulfate-dependent manner. To examine its biological activity in vivo, rMuFGF-18 was injected into normal mice and ectopically overexpressed in transgenic mice by using a liver-specific promoter. Injection of rMuFGF-18 induced proliferation in a wide variety of tissues, including tissues of both epithelial and mesenchymal origin. The two tissues which appeared to be the primary targets of FGF-18 were the liver and small intestine, both of which exhibited histologic evidence of proliferation and showed significant gains in organ weight following 7 (sometimes 3) days of FGF-18 treatment. Transgenic mice that overexpressed FGF-18 in the liver also exhibited an increase in liver weight and hepatocellular proliferation. These results suggest that FGF-18 is a pleiotropic growth factor that stimulates proliferation in a number of tissues, most notably the liver and small intestine.

Indexed as

3T3 CellsAmino Acid SequenceAnimalsBase SequenceCell DivisionCell Line, TransformedCells, CulturedCloning, MolecularDNA, ComplementaryEscherichia coliFibroblast Growth FactorsGene ExpressionHumansIntestine, SmallLiverMiceDNA, Complementaryfibroblast growth factor 18Fibroblast Growth FactorsRecombinant Fusion Proteins

Identifiers

PMID9742123
PMCPMC109192
OpenAlexW2120727763

What OpenQuestion holds

Textmetadata
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.