Evidence map›Paper›PMID 39187316›Full record

ArticleIn vivo (Athens, Greece)

Non-Invasive Direct Visualization of Luciferase-Luciferin Emitted Light Producing True Images from an Orthotopic Lung Cancer Xenograft Model in Nude Mice Using an Ultra-sensitive Low-light Camera and Optics.

Kohei Mizuta, Sean Gallagher, April Wang, Neil Chang, Sei Morinaga, Motokazu Sato, Byung Mo Kang, Robert M Hoffman

Abstract read
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Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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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

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0 citing papers in PubMed.

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4 · The record

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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

8 authors.

Kohei MizutaAntiCancer Inc., San Diego, CA, U.S.A.
Sean GallagherAnalytik Jena, Upland, CA, U.S.A.
April WangAnalytik Jena, Upland, CA, U.S.A.
Neil ChangAnalytik Jena, Upland, CA, U.S.A.
Sei MorinagaAntiCancer Inc., San Diego, CA, U.S.A.
Motokazu SatoAntiCancer Inc., San Diego, CA, U.S.A.
Byung Mo KangAntiCancer Inc., San Diego, CA, U.S.A.
Robert M HoffmanAntiCancer Inc., San Diego, CA, U.S.A.; all@anticancer.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimIn vivo imaging with luciferase-luciferin has been limited by the inability to visualize the low emitted light, with the signal quantified only by photon counting using a cumbersome highly-cooled CCD camera in a dark room. In the present study, we demonstrate direct visualization of the luciferase-luciferin signal from an orthotopic lung cancer in a nude-mouse xenograft model with a sensitive low-light camera and optics. MATERIALS AND

methodsMouse Lewis-lung carcinoma cells expressing luciferase (LL/2-Luc2) were injected transcutaneously into the lung of a nude mouse. One week later after cell injection, luciferase imaging for emission at 560 nm was performed using the UVP Biospectrum Advanced system after i.v. injection of D-luciferin potassium salt. The intensity of the visualized light was measured and quantified with the instrument.

resultsA week following the implantation of LL/2-Luc2 cells in nude mice, the luciferase-luciferin signal from LL/2-Luc2 tumors in the lung was sufficiently visible through the skin to produce true images. At fifteen minutes, the intensity peaked and then progressively dropped due to clearance of luciferin from the tumor.

conclusionUsing the UVP Biospectrum Advanced system we demonstrated non-invasive visualization of true images from luciferase-luciferin signals from an orthotopic lung-cancer mouse model. The luciferase-luciferin emitted light was directly visible through the skin which is a major improvement over previous photon counting to detect the luciferase-luciferin signal.

Indexed as

LuciferasesLuminescent MeasurementsLung NeoplasmsMice, NudeAnimalsBenzothiazolesCell Line, TumorDisease Models, AnimalHeterograftsHumansMiceXenograft Model Antitumor AssaysBenzothiazolesD-luciferinLuciferasesdirect visualizationLewis-lung carcinomaLuciferaseluciferinlung cancernon-invasive imagingnude mouseorthotopic

Identifiers

PMID39187316
PMCPMC11363753

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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.