Evidence map›Paper›PMID 19089838›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2009

Single chain epidermal growth factor receptor antibody conjugated nanoparticles for in vivo tumor targeting and imaging.

Lily Yang, Hui Mao, Y Andrew Wang, Zehong Cao, Xianghong Peng, Xiaoxia Wang, Hongwei Duan, Chunchun Ni, Qingan Yuan, Gregory Adams and 4 more

Open access · greenAbstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 118 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
118citing papers in PubMed, 1 pooled it
18.2field-weighted citation impact, top 1% 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

118 citing papers in PubMed, 1 synthesis or guideline pooled it, 356 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Magnetic Cell Targeting for Cardiovascular Tissue Engineering.Tissue engineering. Part B, Reviews · 2025
    Review
  6. Review
  7. Review
  8. Click Chemistry-Based Bioconjugation of Iron Oxide Nanoparticles.Small (Weinheim an der Bergstrasse, Germany) · 2025
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review

58 more citing papers are in PubMed but not listed here.

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

14 authors at 4 institutions in 1 country.

Lily YangDepartment of Surgery, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA 30322, USA. lyang02@emory.edu
Hui Mao
Y Andrew Wang
Zehong Cao
Xianghong Peng
Xiaoxia Wang
Hongwei Duan
Chunchun Ni
Qingan Yuan
Gregory Adams
Mark Q Smith
William C Wood
Xiaohu Gao
Shuming Nie
Emory University · USFox Chase Cancer Center · USOcean NanoTech (United States) · USUniversity of Washington · US

Funding

Tissue and Animal UseU54CA119338 · NCI · EMORY UNIVERSITY · PI SIMONS, JONATHAN W. · 2005 to 2009
$18.4M
Nanotechnology Linking Biomarkers with Cancer BehaviorR01CA108468 · NCI · EMORY UNIVERSITY · PI NIE, SHUMING · 2004 to 2008
$6.9M
NCI NIH HHS BC 021952NCI NIH HHS R01 CA108468NCI NIH HHS U54 CA119338NCI NIH HHS U54 CA119338-01
6 · The paper itself

Abstract

Epidermal growth factor receptor (EGFR) targeted nanoparticle are developed by conjugating a single-chain anti-EGFR antibody (ScFvEGFR) to surface functionalized quantum dots (QDs) or magnetic iron oxide (IO) nanoparticles. The results show that ScFvEGFR can be successfully conjugated to the nanoparticles, resulting in compact ScFvEGFR nanoparticles that specifically bind to and are internalized by EGFR-expressing cancer cells, thereby producing a fluorescent signal or magnetic resonance imaging (MRI) contrast. In vivo tumor targeting and uptake of the nanoparticles in human cancer cells is demonstrated after systemic delivery of ScFvEGFR-QDs or ScFvEGFR-IO nanoparticles into an orthotopic pancreatic cancer model. Therefore, ScFvEGFR nanoparticles have potential to be used as a molecular-targeted in vivo tumor imaging agent. Efficient internalization of ScFvEGFR nanoparticles into tumor cells after systemic delivery suggests that the EGFR-targeted nanoparticles can also be used for the targeted delivery of therapeutic agents.

Indexed as

AnimalsAntibodiesAntineoplastic AgentsChemistry, PharmaceuticalDrug Delivery SystemsErbB ReceptorsFemaleFerric CompoundsHumansMagnetic Resonance ImagingMiceMice, NudeNanoparticlesNeoplasmsNeoplasm TransplantationPancreatic NeoplasmsAntibodiesAntineoplastic AgentsErbB ReceptorsFerric Compoundsferric oxide

Identifiers

PMID19089838
PMCPMC3626261
OpenAlexW2011690386

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.