Evidence map›Paper›PMID 18157579›Full record

ArticleMolecular imaging and biology

Non-invasive PET imaging of EGFR degradation induced by a heat shock protein 90 inhibitor.

Gang Niu, Weibo Cai, Kai Chen, Xiaoyuan Chen

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular imaging and biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  6. Molecular targeting of CEACAM6 using antibody probes of different sizes.Journal of controlled release : official journal of the Controlled Release Society · 2012
    Article
  7. PET imaging of EGF receptors using [18F]FBEM-EGF in a head and neck squamous cell carcinoma model.European journal of nuclear medicine and molecular imaging · 2012
    Article
  8. Article
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  11. Review
  12. Review
  13. Article
  14. Inhibition of Hsp90 activates osteoclast c-Src signaling and promotes growth of prostate carcinoma cells in bone.Proceedings of the National Academy of Sciences of the United States of America · 2008
    Article
  15. 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.

Gang NiuThe Molecular Imaging Program at Stanford, Department of Radiology and Bio-X Program, Stanford University School of Medicine, 1201 Welch Rd, P095, Stanford, CA 94305-5484, USA.
Weibo Cai
Kai Chen
Xiaoyuan Chen
Stanford University · US

Funding

Stanford Nanocharacterization LaboratoryU54CA119367 · NCI · STANFORD UNIVERSITY · PI GAMBHIR, SANJIV S · 2006 to 2010
$19.8M
Small Animal ImagingP50CA114747 · NCI · STANFORD UNIVERSITY · PI GAMBHIR, SANJIV S · 2005 to 2014
$18.2M
Imaging Alpha (v)beta(3) Integrin ExpressionR21CA102123 · NCI · STANFORD UNIVERSITY · PI CHEN, XIAOYUAN · 2005 to 2006
$365k
MicroPET and NIR Fluorescence Imaging Tumor AngiogenesisR21EB001785 · NIBIB · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHEN, XIAOYUAN · 2003 to 2004
$319k
NCI NIH HHS P50 CA114747NCI NIH HHS R21 CA102123NCI NIH HHS R24 CA93862NCI NIH HHS U54 CA119367NIBIB NIH HHS R21 EB001785
6 · The paper itself

Abstract

purposeThe aim of this study is to non-invasively monitor the epidermal growth factor receptor (EGFR) response to a Hsp90 inhibitor-17-AAG treatment in a PC-3 prostate cancer model. PROCEDURES: Nude mice bearing PC-3 tumor were injected intraperitoneally with 17-AAG and then imaged with micro positron emission tomography (microPET) using (64)Cu-DOTA-cetuximab. Biodistribution studies, immunofluorescence staining, and Western blot were performed to validate the microPET results.

resultsPC-3 cells are sensitive to 17-AAG treatment in a dose-dependent manner. Quantitative microPET showed that (64)Cu-DOTA-cetuximab has prominent tumor activity accumulation in untreated tumors (14.6 +/- 2.6%ID/g) but significantly lower uptake in 17-AAG-treated tumors (8.9 +/- 1.6% ID/g) at 24 h post-injection. Both immunofluorescence staining and Western blot confirmed the significantly lower EGFR expression level in the tumor tissue upon 17-AAG treatment.

conclusionsThe early response to anti-Hsp90 therapy was successfully monitored by quantitative PET using (64)Cu-DOTA-cetuximab, which indicates that this approach may be valuable in monitoring the therapeutic response to Hsp90 inhibitor 17-AAG in EGFR-positive cancer patients.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsBenzoquinonesCell DeathCell Line, TumorCell ProliferationCetuximabErbB ReceptorsFluorescent Antibody TechniqueHeterocyclic Compounds, 1-RingHSP90 Heat-Shock ProteinsHumansLactams, MacrocyclicMice1,4,7,10-tetraazacyclododecane- 1,4,7,10-tetraacetic acidAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsBenzoquinonesCetuximabErbB ReceptorsHeterocyclic Compounds, 1-RingHSP90 Heat-Shock ProteinsLactams, Macrocyclictanespimycin

Identifiers

PMID18157579
OpenAlexW2094031242

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.