Evidence map›Paper›PMID 11250709›Full record

ReviewBreast cancer research : BCR2000

Tyrosine kinase signalling in breast cancer: fibroblast growth factors and their receptors.

C Dickson, B Spencer-Dene, C Dillon, V Fantl

2 registry-linked trialsOpen access · goldAbstract readReview
In one paragraph

Review in Breast cancer research : BCR, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.8field-weighted citation impact, top 15% 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.

NCT02558348 phase1 / phase2terminatednot on this mapstarted 2015, after this paper: background citation

A Phase 1/2a Evaluation of the Safety, Pharmacokinetics and Efficacy of AL3818, a Dual Receptor Tyrosine Kinase Inhibitor, in Subjects With Recurrent or Metastatic Endometrial, Ovarian or Cervical Cancer (AL3818-US-001)

TypeinterventionalSponsorAdvenchen Laboratories, LLCRan2015 to 2017Enrolled12ConditionsEndometrial Cancer, Ovarian Cancer, Cervical CancerArmsAL3818
NCT02584478 phase3unknown statusnot on this mapstarted 2015, after this paper: background citation

A Phase 1/2a/3 Evaluation of the Safety and Efficacy of Adding AL3818 (Anlotinib, INN: Catequentinib), a Dual Receptor Tyrosine Kinase Inhibitor, to Standard Platinum-Based Chemotherapy in Subjects With Recurrent or Metastatic Endometrial, Ovarian, Fallopian, Primary Peritoneal or Cervical Carcinoma

TypeinterventionalSponsorAdvenchen Laboratories, LLCRan2015 to 2024Enrolled294ConditionsEndometrial Carcinoma, Ovarian Carcinoma, Fallopian Tube Carcinoma, Primary Peritoneal CarcinomaArmsAL3818, Paclitaxel, Pegylated Liposomal Doxorubicin (PLD), Topotecan, Carboplatin
3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Beyond VEGF: inhibition of the fibroblast growth factor pathway and antiangiogenesis.Clinical cancer research : an official journal of the American Association for Cancer Research · 2011
    Review
  9. Article
  10. Article
  11. Review
  12. Dendrimer-based tumor cell targeting of fibroblast growth factor-1.Bioorganic & medicinal chemistry letters · 2010
    Article
  13. Article
  14. Review
  15. Review
  16. Genetic susceptibility loci for breast cancer by estrogen receptor status.Clinical cancer research : an official journal of the American Association for Cancer Research · 2008
    Review
  17. Article
  18. Comparative mechanisms of branching morphogenesis in diverse systems.Journal of mammary gland biology and neoplasia · 2006
    Review
  19. Article
  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

4 authors at 2 institutions in 1 country.

C DicksonImperial Cancer Research Fund, London, UK. dickson@icrf.icnet.uk
B Spencer-Dene
C Dillon
V Fantl
The Honourable Society of Lincoln's Inn · GBWorld Cancer Research Fund International · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The fibroblast growth factors [Fgfs (murine), FGFs (human)] constitute a large family of ligands that signal through a class of cell-surface tyrosine kinase receptors. Fgf signalling has been associated in vitro with cellular differentiation as well as mitogenic and motogenic responses. In vivo, Fgfs are critical for animal development, and some have potent angiogenic properties. Several Fgfs have been identified as oncogenes in murine mammary cancer, where their deregulation is associated with proviral insertions of the mouse mammary tumour virus (MMTV). Thus, in some mammary tumours of MMTV-infected mouse strains, integration of viral genomic DNA into the somatic DNA of mammary epithelial cells was found to have caused the inappropriate expression of members of this family of growth factors. Although examination of human breast cancers has shown an altered expression of FGFs or of their receptors in some tumours, their role in the causation of breast disease is unclear and remains controversial.

Indexed as

Signal TransductionAnimalsBreastBreast NeoplasmsFemaleFibroblast Growth FactorsHumansMammary Tumor Virus, MouseMiceOncogenesProtein-Tyrosine KinasesReceptors, Fibroblast Growth FactorFibroblast Growth FactorsProtein-Tyrosine KinasesReceptors, Fibroblast Growth Factor

Identifiers

PMID11250709
PMCPMC138774
OpenAlexW2111121888

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.