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Paper · 21119661

Small molecule FGF receptor inhibitors block FGFR-dependent urothelial carcinoma growth in vitro and in vivo.

Lamont FR and 5 others. Br J Cancer, 2011. Cited by 152 papers, by iCite.

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ConductScience Library. Small molecule FGF receptor inhibitors block FGFR-dependent urothelial carcinoma growth in vitro and in vivo. Papers, record 21119661. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/21119661

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Small molecule FGF receptor inhibitors block FGFR-dependent urothelial carcinoma growth in vitro and in vivo.
PubMed
Journal
Br J Cancer
PubMed
Year
2011
PubMed
Publication types
Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
152
iCite
Relative citation ratio, by iCite
3.45
iCite
Revised in PubMed
2023-11-05
PubMed

Authors6

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Lamont FRF R
2Tomlinson DCD C
3Cooper PAP A
4Shnyder SDS D
5Chester JDJ D
6Knowles MAM A

Source PubMed

Topics25

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
ApoptosisMajor topic
BenzimidazolesMajor topic
Carcinoma, Transitional CellMajor topic
PyrimidinesMajor topic
PyrrolesMajor topic
QuinolonesMajor topic
Receptor, Fibroblast Growth Factor, Type 1Major topic
Receptor, Fibroblast Growth Factor, Type 3Major topic
Urinary Bladder NeoplasmsMajor topic
Animals
Blotting, Western
Cell Cycle
Cell Proliferation
Cells, Cultured
Humans
Immunoenzyme Techniques
In Vitro Techniques
Male
Mice
Mice, Inbred BALB C
Mutation
Phosphorylation
Protein-Tyrosine Kinases
Urothelium
Xenograft Model Antitumor Assays

Source PubMed

Grants2

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

Grant, as the record writes itAgencyCountryNIH projectStated by
C6228/A5437Cancer Research UKUnited KingdomPubMed
C6228/A5569Cancer Research UKUnited KingdomPubMed

Source PubMed

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References46

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
111,276,432Fibroblast growth factors.Genome Biol2001https://conductscience.org/library/papers/11276432PubMed
29,139,660Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors.Science1997https://conductscience.org/library/papers/9139660PubMed
316,619,045Expression of hTERT immortalises normal human urothelial cells without inactivation of the p16/Rb pathway.Oncogene2006https://conductscience.org/library/papers/16619045PubMed
417,384,684Knockdown by shRNA identifies S249C mutant FGFR3 as a potential therapeutic target in bladder cancer.Oncogene2007https://conductscience.org/library/papers/17384684PubMed
516,352,616Molecular subtypes of bladder cancer: Jekyll and Hyde or chalk and cheese?Carcinogenesis2006https://conductscience.org/library/papers/16352616PubMed
69,787,135The t(4;14) translocation in myeloma dysregulates both FGFR3 and a novel gene, MMSET, resulting in IgH/MMSET hybrid transcripts.Blood1998https://conductscience.org/library/papers/9787135PubMed
710,471,491Frequent activating mutations of FGFR3 in human bladder and cervix carcinomas.Nat Genet1999https://conductscience.org/library/papers/10471491PubMed
812,393,535In multiple myeloma, t(4;14)(p16;q32) is an adverse prognostic factor irrespective of FGFR3 expression.Blood2003https://conductscience.org/library/papers/12393535PubMed
919,458,078Fibroblast growth factor receptor 1 promotes proliferation and survival via activation of the mitogen-activated protein kinase pathway in bladder cancer.Cancer Res2009https://conductscience.org/library/papers/19458078PubMed
1011,157,491Activated fibroblast growth factor receptor 3 is an oncogene that contributes to tumor progression in multiple myeloma.Blood2001https://conductscience.org/library/papers/11157491PubMed

Cited by97

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 152 citations.

PMIDTitleJournalYearIn PapersSource
42,177,363FGFR3 oncogenic activation drives oxidative metabolic reprogramming in bladder cancer: a systems metabolomics approach.Commun Biol2026https://conductscience.org/library/papers/42177363PubMed
41,315,241MET signaling drives acquired resistance to erdafitinib in muscle-invasive bladder cancer cells.Cell Death Dis2025https://conductscience.org/library/papers/41315241PubMed
41,179,739Dysregulation of mRNA splicing in urothelial carcinoma: Clinical, diagnostic and therapeutic implications.Bladder Cancer2025https://conductscience.org/library/papers/41179739PubMed
40,603,902FGFR inhibitors promote the autophagic degradation of IFN-γ-induced PD-L1 and alleviate the PD-L1-mediated transcriptional suppression of FGFR3-TACC3 in non-muscle-invasive bladder cancer.Cell Death Dis2025https://conductscience.org/library/papers/40603902PubMed
40,515,475A phase II, multicenter, single-arm study of pemigatinib in patients with metastatic or unresectable colorectal cancer harboring FGFR alterations.Oncologist2025https://conductscience.org/library/papers/40515475PubMed
40,227,644From Bench to Bladder: The Rise in Immune Checkpoint Inhibition in the Treatment of Non-Muscle Invasive Bladder Cancer.Cancers (Basel)2025https://conductscience.org/library/papers/40227644PubMed
40,112,217Targeting COPA to Enhance Erdafitinib Sensitivity in FGFR-Altered Bladder Cancer.Adv Sci (Weinh)2025https://conductscience.org/library/papers/40112217PubMed
39,764,422Targeted therapies and molecular targets in the therapeutic landscape of advanced urothelial carcinoma: state of the art and future perspectives.Explor Target Antitumor Ther2024https://conductscience.org/library/papers/39764422PubMed
39,536,791FGFR Inhibitors in Urothelial Cancer: From Scientific Rationale to Clinical Development.J Korean Med Sci2024https://conductscience.org/library/papers/39536791PubMed
39,031,286The roles of FGFR3 and c-MYC in urothelial bladder cancer.Discov Oncol2024https://conductscience.org/library/papers/39031286PubMed

1 to 10 of 97

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Genes9

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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