Evidence map›Paper›PMID 33830414›Full record

ArticleMolecular imaging and biology2021

Bioluminescent Tumor Signal Is Mouse Strain and Pelt Color Dependent: Experience in a Disseminated Lymphoma Model.

Mark J Hoegger, Mark S Longtine, Kyuhwan Shim, Richard L Wahl

Open access · greenAbstract read
In one paragraph

Article in Molecular imaging and biology, 2021. 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
0.2field-weighted citation impact, top 48% 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, 3 citations in OpenAlex.

  1. Cure of Disseminated Human Lymphoma with [Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2023
    Article
  2. Cure of Disseminated Human Lymphoma with [Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2023
    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

4 authors at 1 institution in 1 country.

Mark J HoeggerMallinckrodt Institute of Radiology, Washington University School of Medicine, Campus Box 8131, 510 South Kingshighway Boulevard, St Louis, MO, 63110, USA.ORCID 0000-0002-8214-8177
Mark S LongtineMallinckrodt Institute of Radiology, Washington University School of Medicine, Campus Box 8131, 510 South Kingshighway Boulevard, St Louis, MO, 63110, USA.
Kyuhwan ShimMallinckrodt Institute of Radiology, Washington University School of Medicine, Campus Box 8131, 510 South Kingshighway Boulevard, St Louis, MO, 63110, USA.
Richard L WahlMallinckrodt Institute of Radiology, Washington University School of Medicine, Campus Box 8131, 510 South Kingshighway Boulevard, St Louis, MO, 63110, USA. r.wahl@wustl.edu.ORCID 0000-0002-7306-2590
Mallinckrodt (United States) · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Training OPportunities in Translational Imaging Education and Research (TOP-TIER)T32EB021955 · NIBIB · WASHINGTON UNIVERSITY · PI Hongyu An, Joseph Edward Ippolito · 2017 to 2026
$2.4M
NCI NIH HHS P30 CA091842NIBIB NIH HHS T32 EB021955
6 · The paper itself

Abstract

backgroundMany preclinical cancer studies use mice with varied phenotypes to monitor tumor treatment. We compared survival and optical imaging characteristics of strains with varied coat colors harboring luciferase-expressing disseminated lymphoma.

resultsLuciferase-expressing lymphoma cells (Raji-luc) were injected via tail vein into severe combined immunodeficient (SCID) and Rag2-IL2rg (R2G2) mice, and survival was tracked. Tumor signals were obtained by imaging ventral and dorsal aspects of mice. Signal attenuation by isolated mouse pelts was measured in vitro. R2G2 mice had decreased survival compared to SCID mice (17 vs. 32 days, p<0.001) despite similar bioluminescence signal when mice were imaged dorsally (p=0.37). However, signal was 17.3-fold higher in R2G2 mice compared to SCID (p<0.001) when imaged ventrally. Isolated dark R2G2 dorsal pelts attenuated signal more than ventral pelts when placed over cells in vitro.

conclusionsMouse pelt color and imaging aspect are critical considerations for quantifying bioluminescent tumor signal, and the R2G2 mouse strain may prove useful for preclinical targeted therapy studies.

Indexed as

LymphomaAnimalsCell LineDisease Models, AnimalFemaleHairLuminescent MeasurementsMiceMice, SCIDMice, TransgenicRadiotherapySkin PigmentationBioluminescent imagingLymphomaMicePreclinical cancer therapyTargeted radionuclide therapy

Identifiers

PMID33830414
PMCPMC8410647
OpenAlexW3140539229

What OpenQuestion holds

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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.