Evidence map›Paper›PMID 30326563›Full record

ArticleInternational journal of molecular sciences2018

BGJ398, A Pan-FGFR Inhibitor, Overcomes Paclitaxel Resistance in Urothelial Carcinoma with FGFR1 Overexpression.

Se Hyun Kim, Haram Ryu, Chan-Young Ock, Koung Jin Suh, Ji Yun Lee, Ji-Won Kim, Jeong-Ok Lee, Jin Won Kim, Yu Jung Kim, Keun-Wook Lee and 6 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Pharmacological and Biological Targeting of FGFR1 in Cancer.Current issues in molecular biology · 2024
    Review
  5. Article
  6. Frontiers in oncology · 2023
    Article
  7. Article
  8. Predicting patient response with models trained on cell lines and patient-derived xenografts by nonlinear transfer learning.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  9. Review
  10. Article
  11. Article
  12. Role of tyrosine kinases in bladder cancer progression: an overview.Cell communication and signaling : CCS · 2020
    Review
  13. Synthesis, biological evaluations and molecular modelling studies of novel indolin-2-ones designing as FGFR inhibitors.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2019
    Article
  14. Article
  15. [Molecular tumor board-urothelial cancer].Der Urologe. Ausg. A · 2019
    Review
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

16 authors at 2 institutions in 1 country.

Se Hyun KimDivision of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea. sehyunkim@snubh.org.ORCID 0000-0002-2292-906X
Haram RyuMedical Research Collaborating Center, Seoul National University Bundang Hospital, Seongnam 13605, Korea. r2218@snubh.org.
Chan-Young OckDivision of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea. ock.chanyoung@gmail.com.
Koung Jin SuhDivision of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea. skjmd0919@snubh.org.
Ji Yun LeeDivision of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea. maimatin83@snubh.org.
Ji-Won KimDivision of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea. jiwonkim@snubh.org.ORCID 0000-0001-6426-9074
Jeong-Ok LeeDivision of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea. deafkeller@snubh.org.
Jin Won KimDivision of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea. jwkim@snubh.org.
Yu Jung KimDivision of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea. cong1005@snubh.org.
Keun-Wook LeeDivision of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea. hmodoctor@snubh.org.
Soo-Mee BangDivision of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea. 65368@snubh.org.
Jee Hyun KimDivision of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea. jhkimmd@snubh.org.
Jong Seok LeeDivision of Hematology and Medical Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea. jslee@snubh.org.
Joong Bae AhnDivision of Medical Oncology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Korea. vvswm513@yuhs.ac.
Kui-Jin KimMedical Research Collaborating Center, Seoul National University Bundang Hospital, Seongnam 13605, Korea. 99264@snubh.org.
Sun Young RhaDivision of Medical Oncology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Korea. rha7655@yuhs.ac.
Seoul National University Bundang Hospital · KRYonsei University · KR

Funding

National Research Foundation of Korea 2016R1D1A1B03932800
6 · The paper itself

Abstract

Paclitaxel (PTX) is commonly used to treat urothelial carcinoma (UC) after platinum-based chemotherapy has failed. However, single-agent taxane therapy is not sufficient to inhibit tumor progression and drug resistance in advanced UC. Epithelial-to-mesenchymal transition (EMT) induced by fibroblast growth factor receptor (

Indexed as

Gene ExpressionCell Line, TumorCell MovementCell SurvivalDrug Resistance, NeoplasmDrug SynergismEpithelial-Mesenchymal TransitionGene Expression ProfilingHumansPaclitaxelPhenylurea CompoundsProtein Kinase InhibitorsPyrimidinesReceptor, Fibroblast Growth Factor, Type 1Signal TransductionTranscriptomeFGFR1 protein, humaninfigratinibPaclitaxelPhenylurea CompoundsProtein Kinase InhibitorsPyrimidinesReceptor, Fibroblast Growth Factor, Type 1BGJ398combination therapyepithelial-to-mesenchymal transitionFGFRFGFR inhibitorpaclitaxelurothelial carcinoma

Identifiers

PMID30326563
PMCPMC6214101
OpenAlexW2896050619

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.