Evidence map›Paper›PMID 29463820›Full record

ArticleScientific reports2018

Correlation of 360-degree Surface Mapping In Vivo Bioluminescence with Multi-Spectral Optoacoustic Tomography in Human Xenograft Tumor Models.

Andrew Brannen, Matthew Eggert, Matthias Nahrendorf, Robert Arnold, Peter Panizzi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 57% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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 at 2 institutions in 1 country.

Andrew BrannenDepartment of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, 247 Pharmacy Research Building, 720 South Donahue Dr., Auburn, AL, 36849, USA.ORCID 0000-0002-1318-2304
Matthew EggertDepartment of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, 247 Pharmacy Research Building, 720 South Donahue Dr., Auburn, AL, 36849, USA.ORCID 0000-0003-0148-3174
Matthias NahrendorfCenter for Systems Biology, Massachusetts General Hospital & Harvard Medical School, 185 Cambridge Street, Boston, MA, 02115, USA.
Robert ArnoldDepartment of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, 247 Pharmacy Research Building, 720 South Donahue Dr., Auburn, AL, 36849, USA.ORCID 0000-0001-6143-3991
Peter PanizziDepartment of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, 247 Pharmacy Research Building, 720 South Donahue Dr., Auburn, AL, 36849, USA. panizzi@auburn.edu.ORCID 0000-0003-0141-8807
Auburn University · USHarvard University · US

Funding

Pathogen specific imaging of endocarditisR01HL114477 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI NAHRENDORF, MATTHIAS, PANIZZI, PETER ROLF · 2013 to 2016
$1.7M
Secretory Phospholipases sPLA2 and their Receptors for Delivering NanoparticlesR01EB016100 · NIBIB · AUBURN UNIVERSITY AT AUBURN · PI ARNOLD, ROBERT D · 2013 to 2016
$1.3M
NHLBI NIH HHS R01 HL114477NIBIB NIH HHS R01 EB016100
6 · The paper itself

Abstract

Pre-clinical monitoring of tumor growth and identification of distal metastasis requires a balance between accuracy and expediency. Bioluminescence imaging (BLI) is often used to track tumor growth but is primarily limited to planar 2-dimensional (2D) imaging. Consistent subject placement within a standard top-mounted, single-detector small animal imager is vital to reducing variability in repeated same-animal measures over time. Here, we describe a method for tracking tumor development using a multi-angle BLI and photo-acoustic workflow. We correlate serial caliper measurements and 2D BLI to 360° BLI and photo-acoustic datasets for the same animals. Full 360° BLI showed improved correlations with both volumes obtained from caliper measurements and photo-acoustic segmentation, as compared to planar BLI. We also determined segmented tumor volumes from photo-acoustic datasets more accurately reflects true excised tumors' volumes compared to caliper measurements. Our results demonstrate the distinct advantages of both 360° surface mapping by BLI and photo-acoustic methodologies for non-invasive tracking of tumor growth in pre-clinical academic settings. Furthermore, our design is fully implementable in all top-mounted, single-detector imagers, thereby providing the opportunity to shift the paradigm away from planar BLI into rapid BLI tomography applications.

Indexed as

AnimalsBreast NeoplasmsFemaleHumansImage Processing, Computer-AssistedLuminescent MeasurementsMiceMice, NudePhotoacoustic TechniquesTumor BurdenTumor Cells, CulturedXenograft Model Antitumor Assays

Identifiers

PMID29463820
PMCPMC5820276
OpenAlexW2791951063

What OpenQuestion holds

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LicenceCC BY
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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.