Evidence map›Paper›PMID 24398510›Full record

ArticleBritish journal of cancer2014

Inhibition of OATP1B1 by tyrosine kinase inhibitors: in vitro-in vivo correlations.

S Hu, R H J Mathijssen, P de Bruijn, S D Baker, A Sparreboom

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 54 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Pharmacogenomics in Cytotoxic Chemotherapy of Cancer.Methods in molecular biology (Clifton, N.J.) · 2022
    Review
  11. Regulation of OATP1B1 Function by Tyrosine Kinase-mediated Phosphorylation.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  12. Article
  13. Article
  14. Review
  15. Role of Oatp2b1 in Drug Absorption and Drug-Drug Interactions.Drug metabolism and disposition: the biological fate of chemicals · 2020
    Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

S HuDepartment of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
R H J MathijssenDepartment of Medical Oncology, Erasmus University Medical Center, Rotterdam, The Netherlands.
P de BruijnDepartment of Medical Oncology, Erasmus University Medical Center, Rotterdam, The Netherlands.
S D BakerDepartment of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
A Sparreboom1] Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN 38105, USA [2] Department of Medical Oncology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Erasmus MC · NLSt. Jude Children's Research Hospital · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
NCI NIH HHS 3P30CA021765NCI NIH HHS P30 CA021765
6 · The paper itself

Abstract

backgroundSeveral tyrosine kinase inhibitors (TKIs) can decrease docetaxel clearance in patients by an unknown mechanism. We hypothesised that these interactions are mediated by the hepatic uptake transporter OATP1B1.

methodsThe influence of 16 approved TKIs on transport was studied in vitro using HEK293 cells expressing OATP1B1 or its mouse equivalent Oatp1b2. Pharmacokinetic studies were performed with Oatp1b2-knockout and OATP1B1-transgenic mice.

resultsAll docetaxel-interacting TKIs, including sorafenib, were identified as potent inhibitors of OATP1B1 in vitro. Although Oatp1b2 deficiency in vivo was associated with increased docetaxel exposure, single- or multiple-dose sorafenib did not influence docetaxel pharmacokinetics.

conclusionThese findings highlight the importance of identifying proper preclinical models for verifying and predicting TKI-chemotherapy interactions involving transporters.

Indexed as

AnimalsBiological TransportDocetaxelDrug InteractionsHEK293 CellsHepatocytesHumansLiverLiver-Specific Organic Anion Transporter 1MiceMice, KnockoutNiacinamideOrganic Anion TransportersOrganic Anion Transporters, Sodium-IndependentPhenylurea CompoundsProtein Kinase InhibitorsDocetaxelLiver-Specific Organic Anion Transporter 1NiacinamideOrganic Anion TransportersOrganic Anion Transporters, Sodium-IndependentPhenylurea CompoundsProtein Kinase InhibitorsProtein-Tyrosine KinasesSLCO1B1 protein, humanSlco1b2 protein, mouseSorafenibTaxoids

Identifiers

PMID24398510
PMCPMC3929889
OpenAlexW1975051553

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.