Evidence map›Paper›PMID 23097630›Full record

ArticleNeoplasia (New York, N.Y.)2012

Tumor angiogenesis phenotyping by nanoparticle-facilitated magnetic resonance and near-infrared fluorescence molecular imaging.

Peter A Jarzyna, Lisette H Deddens, Benjamin H Kann, Sarayu Ramachandran, Claudia Calcagno, Wei Chen, Anita Gianella, Rick M Dijkhuizen, Arjan W Griffioen, Zahi A Fayad and 1 more

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Detecting vascular normalization in epithelial ovarian cancer.Medical oncology (Northwood, London, England) · 2025
    Review
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  5. Journal of nanobiotechnology · 2019
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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

11 authors at 4 institutions in 2 countries.

Peter A JarzynaTranslational and Molecular Imaging Institute, Mount Sinai School of Medicine, New York, NY 10029, USA.
Lisette H Deddens
Benjamin H Kann
Sarayu Ramachandran
Claudia Calcagno
Wei Chen
Anita Gianella
Rick M Dijkhuizen
Arjan W Griffioen
Zahi A Fayad
Willem J M Mulder
Icahn School of Medicine at Mount Sinai · USUniversity Medical Center Utrecht · NLAmsterdam UMC Location VUmc · NLHarvard University · US

Funding

A Surface Activable Nanoemulsion platform for Breast Cancer Diagnosis and TherapyR01CA155432 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MULDER, WILLEM · 2011 to 2015
$1.7M
NCI NIH HHS R01 CA155432NHLBI NIH HHS HHSN268201000045C
6 · The paper itself

Abstract

One of the challenges of tailored antiangiogenic therapy is the ability to adequately monitor the angiogenic activity of a malignancy in response to treatment. The α(v)β(3) integrin, highly overexpressed on newly formed tumor vessels, has been successfully used as a target for Arg-Gly-Asp (RGD)-functionalized nanoparticle contrast agents. In the present study, an RGD-functionalized nanocarrier was used to image ongoing angiogenesis in two different xenograft tumor models with varying intensities of angiogenesis (LS174T > EW7). To that end, iron oxide nanocrystals were included in the core of the nanoparticles to provide contrast for T(2)*-weighted magnetic resonance imaging (MRI), whereas the fluorophore Cy7 was attached to the surface to enable near-infrared fluorescence (NIRF) imaging. The mouse tumor models were used to test the potential of the nanoparticle probe in combination with dual modality imaging for in vivo detection of tumor angiogenesis. Pre-contrast and post-contrast images (4 hours) were acquired at a 9.4-T MRI system and revealed significant differences in the nanoparticle accumulation patterns between the two tumor models. In the case of the highly vascularized LS174T tumors, the accumulation was more confined to the periphery of the tumors, where angiogenesis is predominantly occurring. NIRF imaging revealed significant differences in accumulation kinetics between the models. In conclusion, this technology can serve as an in vivo biomarker for antiangiogenesis treatment and angiogenesis phenotyping.

Indexed as

Magnetic Resonance ImagingMolecular ImagingNanoparticlesNeovascularization, PathologicSpectroscopy, Near-InfraredAnimalsBone NeoplasmsColorectal NeoplasmsContrast MediaDisease Models, AnimalFluorescenceHumansImmunoenzyme TechniquesIntegrin alphaVbeta3MiceOligopeptidesarginyl-glycyl-aspartic acidContrast MediaIntegrin alphaVbeta3Oligopeptides

Identifiers

PMID23097630
PMCPMC3479840
OpenAlexW2107638043

What OpenQuestion holds

Textmetadata
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.