Evidence map›Paper›PMID 28231806›Full record

ArticleJournal of translational medicine2017

Imatinib increases oxygen delivery in extracellular matrix-rich but not in matrix-poor experimental carcinoma.

Mikhail Burmakin, Tijs van Wieringen, P Olof Olsson, Linda Stuhr, Aive Åhgren, Carl-Henrik Heldin, Rolf K Reed, Kristofer Rubin, Carina Hellberg

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  5. Review
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  7. The role of collagen in cancer: from bench to bedside.Journal of translational medicine · 2019
    Review
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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

9 authors at 3 institutions in 3 countries.

Mikhail BurmakinLudwig Institute for Cancer Research, Science for Life Laboratory, Uppsala University, 751 24, Uppsala, Sweden.
Tijs van WieringenLudwig Institute for Cancer Research, Science for Life Laboratory, Uppsala University, 751 24, Uppsala, Sweden.
P Olof OlssonDepartment of Laboratory Medicine, Medicon Village, Lund University, 223 63, Lund, Sweden.
Linda StuhrDepartment of Biomedicine, University of Bergen, Bergen, Norway.
Aive ÅhgrenLudwig Institute for Cancer Research, Science for Life Laboratory, Uppsala University, 751 24, Uppsala, Sweden.
Carl-Henrik HeldinLudwig Institute for Cancer Research, Science for Life Laboratory, Uppsala University, 751 24, Uppsala, Sweden.
Rolf K ReedDepartment of Biomedicine, University of Bergen, Bergen, Norway.
Kristofer RubinDepartment of Laboratory Medicine, Medicon Village, Lund University, 223 63, Lund, Sweden. Kristofer.Rubin@med.lu.se.ORCID 0000-0003-2789-6276
Carina HellbergLudwig Institute for Cancer Research, Science for Life Laboratory, Uppsala University, 751 24, Uppsala, Sweden.
Uppsala University · SELund University · SEUniversity of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImatinib causes increased turnover of stromal collagen, reduces collagen fibril diameter, enhances extracellular fluid turnover and lowers interstitial fluid pressure (IFP) in the human colonic carcinoma KAT-4/HT-29 (KAT-4) xenograft model.

methodsWe compared the effects of imatinib on oxygen levels, vascular morphology and IFP in three experimental tumor models differing in their content of a collagenous extracellular matrix.

resultsNeither the KAT4 and CT-26 colonic carcinoma models, nor B16BB melanoma expressed PDGF β-receptors in the malignant cells. KAT-4 tumors exhibited a well-developed ECM in contrast to the other two model systems. The collagen content was substantially higher in KAT-4 than in CT-26, while collagen was not detectable in B16BB tumors. The pO

conclusionOur data suggest that the effects of imatinib on pO

Indexed as

AnimalsApoptosisCell Line, TumorCollagenColonic NeoplasmsExtracellular FluidExtracellular MatrixImatinib MesylateMice, SCIDNeoplasms, ExperimentalOxygenPressureReceptor, Platelet-Derived Growth Factor betaStromal CellsTumor BurdenWaterCollagenImatinib MesylateOxygenReceptor, Platelet-Derived Growth Factor betaWaterHypoxiaInterstitial fluid pressureReceptor tyrosine kinaseTumor stroma

Identifiers

PMID28231806
PMCPMC5324310
OpenAlexW2590937891

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.