Evidence map›Paper›PMID 19962894›Full record

ArticleBioorganic & medicinal chemistry letters2010

Dendrimer-based tumor cell targeting of fibroblast growth factor-1.

Thommey P Thomas, Rameshwer Shukla, Alina Kotlyar, Jola Kukowska-Latallo, James R Baker

Open access · greenAbstract read
In one paragraph

Article in Bioorganic & medicinal chemistry letters, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. A multivalent probe for AI-2 quorum-sensing receptors.Journal of the American Chemical Society · 2011
    Article
  10. Structurally Diverse Nitric Oxide-Releasing Poly(propylene Imine) Dendrimers.Chemistry of materials : a publication of the American Chemical Society · 2011
    Article
  11. Article
  12. Review
  13. 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

5 authors at 1 institution in 1 country.

Thommey P ThomasMichigan Nanotechnology Institute for Medicine and Biological Sciences, Department of Internal Medicine, Division of Allergy, University of Michigan, 9220 MSRB III, Box 0648, Ann Arbor, MI 48109, United States. thommey@umich.edu
Rameshwer Shukla
Alina Kotlyar
Jola Kukowska-Latallo
James R Baker
University of Michigan–Ann Arbor · US

Funding

PUBLIC HEALTH DEMONSTRATIONP60DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MYERS, MARTIN G · 1985 to 2012
$26.5M
The Role of Cell Membrane Disruption in Non-Viral Vector Oligonucleotide DeliveryR01EB005028 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BANASZAK HOLL, MARK M · 2006 to 2013
$2.8M
Photonic Crystal Fiber Probe Fluorescence BiosensingR33CA112141 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BAKER, JAMES R. · 2005 to 2007
$1.1M
Photonic crystal technology for biomolecular assayR21RR021893 · NCRR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NORRIS, THEODORE B · 2005 to 2007
$549k
NCI NIH HHS 1 R33 CA112141NCI NIH HHS R33 CA112141NCRR NIH HHS 1 R21 RR021893NCRR NIH HHS R21 RR021893NIBIB NIH HHS R01 EB005028NIDDK NIH HHS 5P60 DK20572NIDDK NIH HHS P60 DK020572
6 · The paper itself

Abstract

Fibroblast Growth Factor Receptor (FGFR) is overexpressed in a wide variety of tumors, and therefore is an attractive target for drug delivery. Recombinant FGF-1 was purified and attached to a fifth-generation (G5) polyamidoamine dendrimer. The specific binding and internalization of this conjugate labeled with FITC was demonstrated by flow cytometry as well as by confocal microscopic analysis in cell lines expressing FGFR. The binding and uptake of FGF-conjugated dendrimers was completely blocked by excess nonconjugated FGF-1. Confocal microscopic analysis showed cytosolic as well as nuclear localization. Multivalent G5-FGF nanoparticles may serve as a platform for cytosolic as well as nuclear drug delivery in tumor cells, and as an FGF delivery agent for angiogenesis and wound healing. Our study shows for the first time the applicability of a dendrimer nanodevice for tumor cell targeting through FGFR.

Indexed as

Antineoplastic AgentsCell Line, TumorCell NucleusDendrimersDrug Delivery SystemsFibroblast Growth Factor 1Flow CytometryFluorescein-5-isothiocyanateHumansNeoplasmsPolyaminesReceptors, Fibroblast Growth FactorRecombinant ProteinsAntineoplastic AgentsDendrimersFibroblast Growth Factor 1Fluorescein-5-isothiocyanatePolyaminesReceptors, Fibroblast Growth FactorRecombinant Proteins

Identifiers

PMID19962894
PMCPMC2818523
OpenAlexW1993707497

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.