Evidence map›Paper›PMID 27986807›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2017

Effects of 4 multitargeted receptor tyrosine kinase inhibitors on regional hemodynamics in conscious, freely moving rats.

Joanne J Carter, Laurice V Fretwell, Jeanette Woolard

Open access · hybridAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Acute vascular and cardiac effects of lenvatinib in mice.Cardio-oncology (London, England) · 2025
    Article
  3. Article
  4. Regionally selective cardiovascular responses to adenosine AFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  5. Article
  6. Article
  7. The effect of two selective ABritish journal of pharmacology · 2020
    Article
  8. Article
  9. Article
  10. Molecular Pharmacology of VEGF-A Isoforms: Binding and Signalling at VEGFR2.International journal of molecular sciences · 2018
    Review
  11. Article
  12. Review
  13. 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

3 authors at 3 institutions in 1 country.

Joanne J CarterCell Signalling Research Group, School of Life Sciences, Medical School, The University of Nottingham, Queen's Medical Centre, Nottingham, United Kingdom; and.
Laurice V FretwellFaculty of Health and Life Sciences, De Montfort University, Leicester, United Kingdom.
Jeanette WoolardCell Signalling Research Group, School of Life Sciences, Medical School, The University of Nottingham, Queen's Medical Centre, Nottingham, United Kingdom; and jeanette.woolard@nottingham.ac.uk.
De Montfort University · GBQueen's Medical Centre · GBUniversity of Nottingham · GB

Funding

Biotechnology and Biological Sciences Research Council BB/L19418
6 · The paper itself

Abstract

VEGF inhibitors, including receptor tyrosine kinase inhibitors, are used as adjunct therapies in a number of cancer treatments. An emerging issue with these drugs is that most cause hypertension. To gain insight into the physiological mechanisms involved, we evaluated their regional hemodynamic effects in conscious rats. Male Sprague Dawley rats (350-450 g) were chronically implanted with pulsed Doppler flow probes (renal and mesenteric arteries, and the descending abdominal aorta) and catheters (jugular vein, peritoneal cavity, and distal abdominal aorta). Regional hemodynamics were measured over 4 d, before and after daily administration of cediranib (3 and 6 mg/kg, 3 and 6 mg/kg/h for 1 h, i.v.), sorafenib (10 and 20 mg/kg, 10 and 20 mg kg/h for 1 h, i.v.), pazopanib (30 and100 mg/kg, i.p.), or vandetanib (12.5 and 25 mg/kg, i.p.). All drugs evoked significant increases (

Indexed as

Adrenergic beta-AntagonistsAngiotensin II Type 1 Receptor BlockersAnimalsConsciousnessHemodynamicsIndazolesIndolesLosartanMaleNiacinamidePhenylurea CompoundsPiperidinesPropranololProtein Kinase InhibitorsPyrimidinesQuinazolinesAdrenergic beta-AntagonistsAngiotensin II Type 1 Receptor BlockerscediranibIndazolesIndolesLosartanNiacinamidepazopanibPhenylurea CompoundsPiperidinesPropranololProtein Kinase InhibitorsPyrimidinesQuinazolinesReceptor Protein-Tyrosine KinasesSorafenibSulfonamidesvandetanibcancer therapyhypertensionregional hemodynamicsRTKIVEGF

Identifiers

PMID27986807
PMCPMC5295730
OpenAlexW2565754769

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.