Evidence map›Paper›PMID 20460527›Full record

ArticleCancer research2010

Intratumoral therapy of glioblastoma multiforme using genetically engineered transferrin for drug delivery.

Dennis J Yoon, Byron H Kwan, Felix C Chao, Theodore P Nicolaides, Joanna J Phillips, Gretchen Y Lam, Anne B Mason, William A Weiss, Daniel T Kamei

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
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  9. Review
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  11. Temozolomide nanoparticles for targeted glioblastoma therapy.ACS applied materials & interfaces · 2015
    Article
  12. Review
  13. Review
  14. Review
  15. Imaging tumor burden in the brain with 89Zr-transferrin.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2013
    Article
  16. Review
  17. Article
  18. The intracellular trafficking pathway of transferrin.Biochimica et biophysica acta · 2012
    Review
  19. Review
  20. 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

9 authors at 3 institutions in 1 country.

Dennis J YoonDepartment of Bioengineering, University of California, Los Angeles, CA 90095, USA.
Byron H Kwan
Felix C Chao
Theodore P Nicolaides
Joanna J Phillips
Gretchen Y Lam
Anne B Mason
William A Weiss
Daniel T Kamei
Neurological Surgery · USUniversity of California, San Francisco · USUniversity of California, Los Angeles · US

Funding

Tissue CoreP50CA097257 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Joseph F Costello · 2002 to 2026
$57.4M
Molecular and Cellular Mechanisms in CancerT32CA108462 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GOGA, ANDREI · 2004 to 2024
$10.4M
Iron Delivery via Blood; Structure Role of TransferrinR01DK021739 · NIDDK · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI MASON, ANNE B. · 1987 to 2011
$3.4M
The role of microglia and macrophages in the development of brain tumorsK08NS063456 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PHILLIPS, JOANNA · 2008 to 2012
$854k
Iron Delivery via Blood; Structural Role of TransferrinR56DK021739 · NIDDK · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI MASON, ANNE B. · 2006 to 2006
$114k
NCI NIH HHS P50 CA097257NCI NIH HHS T32 CA108462NIDDK NIH HHS R01 DK021739NIDDK NIH HHS R01 DK 21739NINDS NIH HHS K08 NS063456
6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is the most common and lethal primary brain tumor with median survival of only 12 to 15 months under the current standard of care. To both increase tumor specificity and decrease nonspecific side effects, recent experimental strategies in the treatment of GBM have focused on targeting cell surface receptors, including the transferrin (Tf) receptor, that are overexpressed in many cancers. A major limitation of Tf-based therapeutics is the short association of Tf within the cell to deliver its payload. We previously developed two mutant Tf molecules, K206E/R632A Tf and K206E/K534A Tf, in which iron is locked into each of the two homologous lobes. Relative to wild-type Tf, we showed enhanced delivery of diphtheria toxin (DT) from these mutants to a monolayer culture of HeLa cells. Here, we extend the application of our Tf mutants to the treatment of GBM. In vitro treatment of Tf mutants to a monolayer culture of glioma cells showed enhanced cellular association as well as enhanced delivery of conjugated DT. Treatment of GBM xenografts with mutant Tf-conjugated DT resulted in pronounced regression in vivo, indicating their potential use as drug carriers.

Indexed as

AnimalsBrain NeoplasmsCell Line, TumorCricetinaeDiphtheria ToxinDrug Delivery SystemsFemaleGenetic EngineeringGlioblastomaHumansImmunotoxinsMiceMice, NudeMutagenesis, Site-DirectedRecombinant ProteinsTransferrinDiphtheria ToxinImmunotoxinsRecombinant ProteinsTransferrin

Identifiers

PMID20460527
PMCPMC2893299
OpenAlexW2107296090

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.