Evidence map›Paper›PMID 27709411›Full record

ArticleMolecular imaging and biology2017

Patterns of Vasculature in Mouse Models of Lung Cancer Are Dependent on Location.

Marta Vilalta, Nicholas P Hughes, Rie Von Eyben, Amato J Giaccia, Edward E Graves

Abstract read
In one paragraph

Article in Molecular imaging and biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. The effect of flow on blood oxygen level dependent (RMagnetic resonance in medicine · 2019
    Article
  12. Article
  13. Deletion ofCancer research · 2019
    Article
  14. Article
  15. 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

5 authors.

Marta VilaltaDepartment of Radiation Oncology, Molecular Imaging Program at Stanford and Bio-X Program, Stanford University, Stanford, CA, USA.
Nicholas P HughesDepartment of Radiation Oncology, Molecular Imaging Program at Stanford and Bio-X Program, Stanford University, Stanford, CA, USA.
Rie Von EybenDepartment of Radiation Oncology, Molecular Imaging Program at Stanford and Bio-X Program, Stanford University, Stanford, CA, USA.
Amato J GiacciaDepartment of Radiation Oncology, Molecular Imaging Program at Stanford and Bio-X Program, Stanford University, Stanford, CA, USA.
Edward E GravesDepartment of Radiation Oncology, Molecular Imaging Program at Stanford and Bio-X Program, Stanford University, Stanford, CA, USA. egraves@stanford.edu.

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Melinda L. Telli · 2007 to 2026
$71.4M
TUMOR HYPOXIA--MOLECULAR STUDIES &CLINICAL EXPLOITATIONP01CA067166 · NCI · STANFORD UNIVERSITY · PI LE, QUYNH-THU XUAN · 1996 to 2017
$25.5M
Radiation-Induced Tumor Cell MigrationR01CA197136 · NCI · STANFORD UNIVERSITY · PI GRAVES, EDWARD E. · 2015 to 2019
$1.9M
Small Animal Image-Guided RadiotherapyR01CA131199 · NCI · STANFORD UNIVERSITY · PI GRAVES, EDWARD E. · 2008 to 2012
$1.6M
NCI NIH HHS P01 CA067166NCI NIH HHS P30 CA124435NCI NIH HHS R01 CA131199NCI NIH HHS R01 CA197136
6 · The paper itself

Abstract

purposePreclinical studies of hypoxia are generally done using ectopic xenograft tumors, which behave differently from human tumors. Our previous findings have shown that subcutaneously implanted lung tumors exhibit more hypoxia than their orthotopic implanted or spontaneous K-ras-induced counterparts. We hypothesize that differences in hypoxia are due to site-specific differences in vascularity and perfusion. PROCEDURES: To compare the presence and functionality of vessels in these tumor models, we studied vascular perfusion in vivo in real time.

resultsOrthotopically implanted and spontaneous K-ras-induced lung tumors showed elevated perfusion, demonstrating vasculature functionality. Little contrast agent uptake was observed within the subcutaneously implanted tumors, indicating vascular dysfunction. These findings were corroborated at the microscopic level with Hoechst 33342 and Meca-32 staining.

conclusionsFrom these observations, we concluded that differences in hypoxia in experimental models is related to vessel perfusion. Thus, appropriate selection of preclinical lung tumor models is essential for the study of hypoxia, angiogenesis and therapies targeting these phenomena.

Indexed as

AnimalsCell Line, TumorDisease Models, AnimalLung NeoplasmsMiceNeoplasm TransplantationPerfusionProto-Oncogene Proteins p21(ras)Signal Processing, Computer-AssistedSubcutaneous TissueHras protein, mouseProto-Oncogene Proteins p21(ras)Non-invasive imaging in animal modelsPreclinical models of cancerTumor microenvironmentVasculatureXenograft models

Identifiers

PMID27709411
PMCPMC5546406

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.