Evidence map›Paper›PMID 20094046›Full record

ReviewNature reviews. Cancer2010

Fibroblast growth factor signalling: from development to cancer.

Nicholas Turner, Richard Grose

3 registry-linked trialsAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Cancer, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 1,416 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,416citing papers in PubMed, 2 pooled it
59.5field-weighted citation impact, top 1% 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.

NCT01496534 phase1terminatednot on this mapstarted 2012, after this paper: background citation

Phase Ib Study of Dovitinib in Combination With Gemcitabine Plus Cisplatin or Gemcitabine Plus Carboplatin in Patients With Advanced Solid Tumors

TypeinterventionalSponsorMatthew GalskyRan2012 to 2013Enrolled14ConditionsSolid Tumors, Bladder CancerArmsCisplatin, Carboplatin
NCT02307500 phase2completednot on this mapstarted 2014, after this paper: background citation

An Open-label Phase II Study of Regorafenib in Patients With Metastatic Solid Tumors Who Have Progressed After Standard Therapy - RESOUND

TypeinterventionalSponsorIstituto Clinico HumanitasRan2014 to 2020Enrolled82ConditionsPancreas Cancer, Ovarian Cancer, Melanoma, SarcomaArmsRegorafenib
NCT03620643 phase2completednot on this mapstarted 2019, after this paper: background citation

Phase II Study of ROS1 Targeting With Crizotinib in Advanced E-cadherin Negative, ER Positive Lobular Breast Cancer, Diffuse Gastric Cancer, Triple Negative Lobular Breast Cancer or CDH1-mutated Solid Tumours

TypeinterventionalSponsorRoyal Marsden NHS Foundation TrustRan2019 to 2024Enrolled33ConditionsLobular Breast Carcinoma, Gastric Cancer, Triple Negative Breast Cancer, CDH1 Gene MutationArmsCrizotinib Oral Capsule [Xalkori], Fulvestrant 50 MG/ML Prefilled Syringe [Faslodex or generic]
3 · Its place in the literature

Who cites it

1,416 citing papers in PubMed, 2 syntheses or guidelines pooled it, 2,644 citations in OpenAlex.

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1,356 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

2 authors at 2 institutions in 1 country.

Nicholas TurnerBreakthrough Breast Cancer Research Centre, The Institute of Cancer Research, London SW3 6JB, UK, and Royal Marsden Hospital, London SW3 6JJ, UK. Nicholas.turner@icr.ac.uk
Richard Grose
Institute of Cancer Research · GBQueen Mary University of London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibroblast growth factors (FGFs) and their receptors control a wide range of biological functions, regulating cellular proliferation, survival, migration and differentiation. Although targeting FGF signalling as a cancer therapeutic target has lagged behind that of other receptor tyrosine kinases, there is now substantial evidence for the importance of FGF signalling in the pathogenesis of diverse tumour types, and clinical reagents that specifically target the FGFs or FGF receptors are being developed. Although FGF signalling can drive tumorigenesis, in different contexts FGF signalling can mediate tumour protective functions; the identification of the mechanisms that underlie these differential effects will be important to understand how FGF signalling can be most appropriately therapeutically targeted.

Indexed as

Cell ProliferationFibroblast Growth FactorsGene AmplificationHumansNeoplasm InvasivenessNeoplasmsReceptors, Fibroblast Growth FactorSignal TransductionTranslocation, GeneticFibroblast Growth FactorsReceptors, Fibroblast Growth Factor

Identifiers

PMID20094046
OpenAlexW1988476050

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.