Evidence map›Paper›PMID 24339736›Full record

ArticleNeoplasia (New York, N.Y.)2013

Mapping in vivo tumor oxygenation within viable tumor by 19F-MRI and multispectral analysis.

Yunzhou Shi, Jason Oeh, Jeffrey Eastham-Anderson, Sharon Yee, David Finkle, Franklin V Peale, Jed Ross, Maj Hedehus, Nicholas van Bruggen, Rayna Venook and 3 more

Abstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2013. 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
–field-weighted citation impact
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.

  1. Review
  2. Perfluorocarbons-BasedInternational journal of nanomedicine · 2020
    Review
  3. Article
  4. Simultaneous spatiotemporal tracking and oxygen sensing of transient implants in vivo using hot-spot MRI and machine learning.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Frontiers in cellular and infection microbiology · 2017
    Article
  10. Article
  11. Review
  12. Biomarkers in preclinical cancer imaging.European journal of nuclear medicine and molecular imaging · 2015
    Review
  13. Article
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

13 authors.

Yunzhou ShiDepartment of Biomedical Imaging, Genentech Inc, South San Francisco, CA.
Jason Oeh
Jeffrey Eastham-Anderson
Sharon Yee
David Finkle
Franklin V Peale
Jed Ross
Maj Hedehus
Nicholas van Bruggen
Rayna Venook
Sarajane Ross
Deepak Sampath
Richard A D Carano

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantifying oxygenation in viable tumor remains a major obstacle toward a better understanding of the tumor micro-environment and improving treatment strategies. Current techniques are often complicated by tumor heterogeneity. Herein, a novel in vivo approach that combines (19)F magnetic resonance imaging ((19)F-MRI) R 1 mapping with diffusion-based multispectral (MS) analysis is introduced. This approach restricts the partial pressure of oxygen (pO2) measurements to viable tumor, the tissue of therapeutic interest. The technique exhibited sufficient sensitivity to detect a breathing gas challenge in a xenograft tumor model, and the hypoxic region measured by MS (19)F-MRI was strongly correlated with histologic estimates of hypoxia. This approach was then applied to address the effects of antivascular agents on tumor oxygenation, which is a research question that is still under debate. The technique was used to monitor longitudinal pO2 changes in response to an antibody to vascular endothelial growth factor (B20.4.1.1) and a selective dual phosphoinositide 3-kinase/mammalian target of rapamycin inhibitor (GDC-0980). GDC-0980 reduced viable tumor pO2 during a 3-day treatment period, and a significant reduction was also produced by B20.4.1.1. Overall, this method provides an unprecedented view of viable tumor pO2 and contributes to a greater understanding of the effects of antivascular therapies on the tumor's microenvironment.

Indexed as

AnimalsCell HypoxiaCell Line, TumorColorectal NeoplasmsFemaleHeterograftsHumansMagnetic Resonance ImagingMiceMice, NudeOxygenPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsTOR Serine-Threonine KinasesTumor MicroenvironmentVascular Endothelial Growth Factor AMTOR protein, humanOxygenPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsTOR Serine-Threonine KinasesVascular Endothelial Growth Factor A

Identifiers

PMID24339736
PMCPMC3858898

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Registered trials

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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.