Evidence map›Paper›PMID 18216218›Full record

ReviewEndocrine reviews2008

Cellular signaling by fibroblast growth factors (FGFs) and their receptors (FGFRs) in male reproduction.

Leanne M Cotton, Moira K O'Bryan, Barry T Hinton

Open access · bronzeAbstract readReview
In one paragraph

Review in Endocrine reviews, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing 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

61 citing papers in PubMed, 130 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. NGF, EPO, and IGF-1 in the Male Reproductive System.Journal of clinical medicine · 2024
    Review
  11. Article
  12. Article
  13. Review
  14. The role of growth factors in human sperm parameters: A review of in vitro studies.International journal of reproductive biomedicine · 2022
    Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

1 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 2 countries.

Leanne M CottonDepartment of Cell Biology, University of Virginia Health Sciences Center, Charlottesville, VA 22908, USA.
Moira K O'Bryan
Barry T Hinton
University of Virginia · USAustralian Research Council · AU

Funding

Lumicrine regulation of epididymal functionR01HD052035 · NICHD · UNIVERSITY OF VIRGINIA · PI HINTON, BARRY T. · 2006 to 2010
$1.3M
NICHD NIH HHS HD 052035NICHD NIH HHS R01 HD052035
6 · The paper itself

Abstract

The major function of the reproductive system is to ensure the survival of the species by passing on hereditary traits from one generation to the next. This is accomplished through the production of gametes and the generation of hormones that function in the maturation and regulation of the reproductive system. It is well established that normal development and function of the male reproductive system is mediated by endocrine and paracrine signaling pathways. Fibroblast growth factors (FGFs), their receptors (FGFRs), and signaling cascades have been implicated in a diverse range of cellular processes including: proliferation, apoptosis, cell survival, chemotaxis, cell adhesion, motility, and differentiation. The maintenance and regulation of correct FGF signaling is evident from human and mouse genetic studies which demonstrate that mutations leading to disruption of FGF signaling cause a variety of developmental disorders including dominant skeletal diseases, infertility, and cancer. Over the course of this review, we will provide evidence for differential expression of FGFs/FGFRs in the testis, male germ cells, the epididymis, the seminal vesicle, and the prostate. We will show that this signaling cascade has an important role in sperm development and maturation. Furthermore, we will demonstrate that FGF/FGFR signaling is essential for normal epididymal function and prostate development. To this end, we will provide evidence for the involvement of the FGF signaling system in the regulation and maintenance of the male reproductive system.

Indexed as

AnimalsFibroblast Growth FactorsHumansMaleReceptors, Fibroblast Growth FactorReproductionSex DifferentiationSignal TransductionTestisFibroblast Growth FactorsReceptors, Fibroblast Growth Factor

Identifiers

PMID18216218
PMCPMC2528845
OpenAlexW2118456468

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.