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Paper · 32315352

INCB054828 (pemigatinib), a potent and selective inhibitor of fibroblast growth factor receptors 1, 2, and 3, displays activity against genetically defined tumor models.

Liu PCC and 26 others. PLoS One, 2020. Cited by 144 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. INCB054828 (pemigatinib), a potent and selective inhibitor of fibroblast growth factor receptors 1, 2, and 3, displays activity against genetically defined tumor models. Papers, record 32315352. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/32315352

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Paper

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

Title
INCB054828 (pemigatinib), a potent and selective inhibitor of fibroblast growth factor receptors 1, 2, and 3, displays activity against genetically defined tumor models.
PubMed
Journal
PLoS One
PubMed
Year
2020
PubMed
Publication types
Journal Article, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
144
iCite
Relative citation ratio, by iCite
6.18
iCite
Revised in PubMed
2020-07-24
PubMed

Authors27

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

OrderAuthorForenameKindORCID iD
1Liu PCCPhillip C C
2Koblish HHolly
3Wu LLiangxing
4Bowman KKevin
5Diamond SSharon
6DiMatteo DDarlise
7Zhang YYue
8Hansbury MMichael
9Rupar MMark
10Wen XXiaoming

1 to 10 of 27Source PubMed

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Topics21

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

MeSH termMajor
MorpholinesMajor topic
NeoplasmsMajor topic
Protein Kinase InhibitorsMajor topic
PyrimidinesMajor topic
PyrrolesMajor topic
Receptor, Fibroblast Growth Factor, Type 1Major topic
Receptor, Fibroblast Growth Factor, Type 2Major topic
Receptor, Fibroblast Growth Factor, Type 3Major topic
Administration, Oral
Animals
Cell Line, Tumor
Female
Half-Life
Humans
Mice
Mice, Inbred C57BL
Mice, Nude
Mice, SCID
Rats
Rats, Nude
Xenograft Model Antitumor Assays

Source PubMed

Grants0

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.

None in this release.

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.

References42

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

OrderPMIDTitleJournalYearIn PapersSource
129,848,605Efficacy of BGJ398, a Fibroblast Growth Factor Receptor 1-3 Inhibitor, in Patients with Previously Treated Advanced Urothelial Carcinoma with FGFR3 Alterations.Cancer Discov2018https://conductscience.org/library/papers/29848605PubMed
221,119,661Small molecule FGF receptor inhibitors block FGFR-dependent urothelial carcinoma growth in vitro and in vivo.Br J Cancer2011https://conductscience.org/library/papers/21119661PubMed
324,550,739Integrated genomic characterization reveals novel, therapeutically relevant drug targets in FGFR and EGFR pathways in sporadic intrahepatic cholangiocarcinoma.PLoS Genet2014https://conductscience.org/library/papers/24550739PubMed
424,393,342Targeted inhibition of the FGF19-FGFR4 pathway in hepatocellular carcinoma; translational safety considerations.Liver Int2014https://conductscience.org/library/papers/24393342PubMed
523,175,443Oncogenic FGFR3 gene fusions in bladder cancer.Hum Mol Genet2013https://conductscience.org/library/papers/23175443PubMed
610,647,931The hallmarks of cancer.Cell2000https://conductscience.org/library/papers/10647931PubMed
720,226,9628p11 myeloproliferative syndrome: a review.Hum Pathol2010https://conductscience.org/library/papers/20226962PubMed
817,912,529Role of FGFR3 in urothelial cell carcinoma: biomarker and potential therapeutic target.World J Urol2007https://conductscience.org/library/papers/17912529PubMed
910,809,780Elevated cholesterol metabolism and bile acid synthesis in mice lacking membrane tyrosine kinase receptor FGFR4.J Biol Chem2000https://conductscience.org/library/papers/10809780PubMed
1022,837,387Transforming fusions of FGFR and TACC genes in human glioblastoma.Science2012https://conductscience.org/library/papers/22837387PubMed

Cited by85

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 144 citations.

PMIDTitleJournalYearIn PapersSource
42,679,332Sequencing of Fibroblast Growth Factor Receptor Inhibitors in Cholangiocarcinoma: A Review of Published Cases.JCO Precis Oncol2026https://conductscience.org/library/papers/42679332PubMed
42,177,363FGFR3 oncogenic activation drives oxidative metabolic reprogramming in bladder cancer: a systems metabolomics approach.Commun Biol2026https://conductscience.org/library/papers/42177363PubMed
42,058,998FGFR alterations and potential role of FGFR inhibitors in pediatric brain tumors.Neurooncol Adv2026https://conductscience.org/library/papers/42058998PubMed
41,420,106Mechanisms of resistance to VHL loss-induced genetic and pharmacological vulnerabilities.EMBO Mol Med2026https://conductscience.org/library/papers/41420106PubMed
41,226,200Protein-Ligand Interactions in Cardiometabolic Drug Targets: Focus on Weight Loss and Cardioprotection.Molecules2025https://conductscience.org/library/papers/41226200PubMed
41,090,357Pharmacologic inhibition of IRE1α-dependent decay protects alveolar epithelial identity and prevents pulmonary fibrosis in mice.J Clin Invest2025https://conductscience.org/library/papers/41090357PubMed
41,084,837Dabogratinib (TYRA-300), an FGFR3 Isoform-Selective Inhibitor: Preclinical and Initial Clinical Evidence of Antitumor Activity.Mol Cancer Ther2026https://conductscience.org/library/papers/41084837PubMed
41,002,392FGFR1 Inhibition by Pemigatinib Enhances Radiosensitivity in Glioblastoma Stem Cells Through S100A4 Downregulation.Cells2025https://conductscience.org/library/papers/41002392PubMed
40,781,553Exploiting collateral sensitivity in the evolution of resistance to tyrosine kinase inhibitors in soft tissue sarcomas.Commun Biol2025https://conductscience.org/library/papers/40781553PubMed
40,762,256Protein kinase B inhibitors enhance the sensitivity of translocated promoter region-fibroblast growth factor receptor 1 cells to fibroblast growth factor receptor 1 inhibitor-induced apoptosis.J Int Med Res2025https://conductscience.org/library/papers/40762256PubMed

1 to 10 of 85

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Genes25

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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