Evidence map›Paper›PMID 26423316›Full record

ArticleNMR in biomedicine2015

Peritumoral tissue compression is predictive of exudate flux in a rat model of cerebral tumor: an MRI study in an embedded tumor.

James R Ewing, Tavarekere N Nagaraja, Madhava P Aryal, Kelly A Keenan, Rasha Elmghirbi, Hassan Bagher-Ebadian, Swayamprava Panda, Mei Lu, Tom Mikkelsen, Glauber Cabral and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in NMR in biomedicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

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  14. The impact of initial tumor microenvironment on imaging phenotype.Cancer treatment and research communications · 2021
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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

11 authors at 3 institutions in 1 country.

James R EwingDepartment of Neurology, Henry Ford Hospital, Detroit, MI, USA.
Tavarekere N NagarajaDepartment of Neurosurgery, Henry Ford Hospital, Detroit, MI, USA.
Madhava P AryalDepartment of Radiation Oncology, University of Michigan Medical School, Ann Arbor, MI, USA.
Kelly A KeenanDepartment of Neurosurgery, Henry Ford Hospital, Detroit, MI, USA.
Rasha ElmghirbiDepartment of Neurology, Henry Ford Hospital, Detroit, MI, USA.
Hassan Bagher-EbadianDepartment of Neurology, Henry Ford Hospital, Detroit, MI, USA.
Swayamprava PandaDepartment of Neurology, Henry Ford Hospital, Detroit, MI, USA.
Mei LuDepartment of Public Health Sciences, Henry Ford Hospital, Detroit, MI, USA.
Tom MikkelsenDepartment of Neurology, Henry Ford Hospital, Detroit, MI, USA.
Glauber CabralDepartment of Neurology, Henry Ford Hospital, Detroit, MI, USA.
Stephen L BrownDepartment of Radiation Oncology, Henry Ford Hospital, Detroit, MI, USA.
Henry Ford Hospital · USMichigan Medicine · USOakland University · US

Funding

MRI Biomarkers of Response in Cerebral TumorsR01CA135329 · NCI · HENRY FORD HEALTH SYSTEM · PI EWING, JAMES R · 2009 to 2013
$1.5M
NCI NIH HHS R01 CA135329NCI NIH HHS R01CA135329
6 · The paper itself

Abstract

MRI estimates of extracellular volume and tumor exudate flux in peritumoral tissue are demonstrated in an experimental model of cerebral tumor. Peritumoral extracellular volume predicted the tumor exudate flux. Eighteen RNU athymic rats were inoculated intracerebrally with U251MG tumor cells and studied with dynamic contrast enhanced MRI (DCE-MRI) approximately 18 days post implantation. Using a model selection paradigm and a novel application of Patlak and Logan plots to DCE-MRI data, the distribution volume (i.e. tissue porosity) in the leaky rim of the tumor and that in the tissue external to the rim (the outer rim) were estimated, as was the tumor exudate flow from the inner rim of the tumor through the outer rim. Distribution volume in the outer rim was approximately half that of the inner adjacent region (p < 1 × 10(-4)). The distribution volume of the outer ring was significantly correlated (R(2) = 0.9) with tumor exudate flow from the inner rim. Thus, peritumoral extracellular volume predicted the rate of tumor exudate flux. One explanation for these data is that perfusion, i.e. the delivery of blood to the tumor, was regulated by the compression of the mostly normal tissue of the tumor rim, and that the tumor exudate flow was limited by tumor perfusion.

Indexed as

AnimalsBrainBrain NeoplasmsCompressive StrengthComputer SimulationExudates and TransudatesImage Interpretation, Computer-AssistedMagnetic Resonance ImagingModels, BiologicalRatsRats, NudeReproducibility of ResultsSensitivity and SpecificityStress, MechanicalDCE-MRIdynamic contrast enhanced MRIinterstitial flowLogan plotPatlak plottumor interstitial volumetumor vasculature

Identifiers

PMID26423316
PMCPMC4656050
OpenAlexW2135984383

What OpenQuestion holds

Textmetadata
LicenceTDM
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.