Evidence map›Paper›PMID 22807580›Full record

ArticleMolecular cancer therapeutics2012

An optical probe for noninvasive molecular imaging of orthotopic brain tumors overexpressing epidermal growth factor receptor.

Richard S Agnes, Ann-Marie Broome, Jing Wang, Anjali Verma, Kari Lavik, James P Basilion

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Fluorescence imaging of MALAT1 expression using a Cy5.5-labeled antisense oligonucleotide in lung cancer and epidermal carcinoma cells.Cancer imaging : the official publication of the International Cancer Imaging Society · 2025
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  9. Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2017
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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

6 authors at 1 institution in 1 country.

Richard S AgnesDepartments of Radiology, Biomedical Engineering, and Pathology, NFCR Center for Molecular Imaging at Case, Case Western Reserve University, Wearn Building, Room B-42, 11100 Euclid Avenue, Cleveland, OH 44106, USA. jxb206@case.edu
Ann-Marie Broome
Jing Wang
Anjali Verma
Kari Lavik
James P Basilion
Case Western Reserve University · US

Funding

Imaging of gene expression in glioblastomaR01CA109620 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI BASILION, JAMES PETER · 2006 to 2010
$1.6M
Northeastern Ohio Animal Imaging Resource Center- NOAIRCU24CA110943 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI DUERK, JEFFREY L. · 2007 to 2008
$1.3M
Dual-Receptor Targeted Nanoparticles for Photodynamic Therapy of Brain CancerR01EB012099 · NIBIB · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BROOME, ANN-MARIE · 2010 to 2013
$1.3M
NCI NIH HHS R01 CA109620NCI NIH HHS R01CA109620NCI NIH HHS U24 CA110943NCI NIH HHS U24CA110943NIBIB NIH HHS R01 EB012099NIBIB NIH HHS R01EB12099
6 · The paper itself

Abstract

We have developed a near-infrared (NIR) probe that targets cells overexpressing the EGF receptor (EGFR) for imaging glioblastoma brain tumors in live subjects. A peptide specific for the EGFR was modified with various lengths of monodiscrete polyethylene glycol (PEG) units and a NIR Cy5.5 fluorescence dye. The lead compound, compound 2, with one unit of PEG displayed good binding (8.9 μmol/L) and cellular uptake in glioblastoma cells overexpressing EGFR in vitro. The in vivo studies have shown that the probe was able to selectively label glioblastoma-derived orthotopic brain tumors. In vivo image analyses of peptide binding to the tumors using fluorescence-mediated molecular tomography revealed that the compound could distinguish between tumors expressing different levels of EGFR. The data presented here represent the first demonstration of differential quantitation of tumors expressing EGFR in live animals by a targeted NIR fluorescence probe using a molecular imaging device.

Indexed as

Optical PhenomenaAmino Acid SequenceAnimalsBrain NeoplasmsCarbocyaninesCell Line, TumorErbB ReceptorsFemaleFluorescent DyesHumansKineticsLigandsMiceMice, NudeMolecular ImagingMolecular Sequence DataCarbocyaninesCY5.5 cyanine dyeErbB ReceptorsFluorescent DyesLigandsPeptides

Identifiers

PMID22807580
PMCPMC3829608
OpenAlexW2122411931

What OpenQuestion holds

Textmetadata
LicenceTDM
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.