Evidence map›Paper›PMID 29289705›Full record

ArticleFree radical biology & medicine2018

Molecular imaging of tumor photoimmunotherapy: Evidence of photosensitized tumor necrosis and hemodynamic changes.

Shun Kishimoto, Nobu Oshima, Kazutoshi Yamamoto, Jeeva Munasinghe, Jan Henrik Ardenkjaer-Larsen, James B Mitchell, Peter L Choyke, Murali C Krishna

Abstract read
In one paragraph

Article in Free radical biology & medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

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  8. HyperpolarizedAntioxidants & redox signaling · 2022
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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

8 authors at 4 institutions in 2 countries.

Shun KishimotoRadiation Biology Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD 20892, United States.
Nobu OshimaUrologic Oncology Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD 20892, United States.
Kazutoshi YamamotoRadiation Biology Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD 20892, United States.
Jeeva MunasingheMouse Imaging Facility, National Institute of Neurological Disease and Stroke, NIH, Bethesda, MD 20892, United States.
Jan Henrik Ardenkjaer-LarsenCenter for Magnetic Resonance, Denmark Technical University, Copenhagen, Denmark.
James B MitchellRadiation Biology Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD 20892, United States.
Peter L ChoykeMolecular Imaging Program, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD 20892, United States.
Murali C KrishnaRadiation Biology Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD 20892, United States. Electronic address: cherukum@mail.nih.gov.
National Cancer Institute · USCenter for Cancer Research · USNational Institute of Neurological Disorders and Stroke · USTechnical University of Denmark · DK

Funding

Time Domian Electron Paramagnetic Resonance ImagingZIABC010476 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CHERUKURI, MURALI · 2009 to 2025
$17.9M
Overhauser Enhanced Magnetic Resonance Imaging (OMRI)ZIABC010477 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CHERUKURI, MURALI · 2009 to 2025
$16.1M
Time Domian Electron Paramagnetic Resonance ImagingZ01BC010476 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CHERUKURI, MURALI · 2003 to 2008
$1.7M
Overhauser Enhanced Magnetic Resonance Imaging (OMRI)Z01BC010477 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CHERUKURI, MURALI · 2003 to 2008
$732k
Intramural NIH HHS Z01 BC010476Intramural NIH HHS Z01 BC010477NCI NIH HHS ZIA BC010477
6 · The paper itself

Abstract

Near-infrared photoimmunotherapy (NIR PIT) employs the photoabsorbing dye IR700 conjugated to antibodies specific for cell surface epidermal growth factor receptor (EGFR). NIR PIT has shown highly selective cytotoxicity in vitro and in vivo. Cell necrosis is thought to be the main mode of cytotoxicity based mainly on in vitro studies. To better understand the acute effects of NIR PIT, molecular imaging studies were performed to assess its cellular and vascular effects. In addition to in vitro studies for cytotoxicity of NIR PIT, the in vivo tumoricidal effects and hemodynamic changes induced by NIR PIT were evaluated by

Indexed as

AnimalsCell Line, TumorErbB ReceptorsFemaleFumaratesHemodynamicsHumansImmunotherapyInfrared RaysMagnetic Resonance ImagingMiceMice, NudeNecrosisOxidation-ReductionPanitumumabPhotoacoustic TechniquesEGFR protein, humanErbB ReceptorsFumaratesPanitumumabPhotosensitizing Agents(13)C MRIHemodynamic changePhotoacoustic imagingPhotoimmunotherapy

Identifiers

PMID29289705
PMCPMC5963721
OpenAlexW2779052889

What OpenQuestion holds

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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.