Evidence map›Paper›PMID 20603862›Full record

ArticleThe journal of gene medicine2010

Silk-elastinlike protein polymers improve the efficacy of adenovirus thymidine kinase enzyme prodrug therapy of head and neck tumors.

Khaled Greish, Jordan Frandsen, Stephanie Scharff, Joshua Gustafson, Joseph Cappello, Daqing Li, Bert W O'Malley, Hamidreza Ghandehari

Abstract read
In one paragraph

Article in The journal of gene medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.1field-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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Silk Fibroin-Based Materials for Catalyst Immobilization.Molecules (Basel, Switzerland) · 2020
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Silk-based biomaterials for sustained drug delivery.Journal of controlled release : official journal of the Controlled Release Society · 2014
    Review
  15. Controlled release from recombinant polymers.Journal of controlled release : official journal of the Controlled Release Society · 2014
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Elastomeric polypeptides.Topics in current chemistry · 2012
    Review
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

8 authors at 4 institutions in 2 countries.

Khaled GreishDepartment of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, UT, USA.
Jordan Frandsen
Stephanie Scharff
Joshua Gustafson
Joseph Cappello
Daqing Li
Bert W O'Malley
Hamidreza Ghandehari
University of Utah · USUniversity of Pennsylvania Health System · USMarine Polymer Technologies (United States) · USPhilipps University of Marburg · DE

Funding

Engineering Polymers For Gene Therapy of Head CancerR01CA107621 · NCI · UNIVERSITY OF UTAH · PI GHANDEHARI, HAMID · 2005 to 2014
$2.5M
NCI NIH HHS R01 CA107621NCI NIH HHS R01-CA107621
6 · The paper itself

Abstract

backgroundAdenoviral-directed enzyme prodrug therapy is a promising approach for head and neck cancer gene therapy. The challenges faced by this approach, however, comprise transient gene expression and dissemination of viruses to distant organs.

methodsWe used recombinant silk-elastinlike protein polymer (SELP) matrices for intratumoral delivery of adenoviruses containing both thymidine kinase-1 and luciferase genes in a nude mouse model of JHU-022 head and neck tumor. Hydrogels made from two SELP analogues (47K and 815K), with similar silk to elastinlike block ratios but different block lengths, were studied for intratumoral viral delivery. Tumor-bearing mice were followed up for tumor progression and luciferase gene expression concomitantly for 5 weeks. Polymer safety was evaluated through body weight change, blood count, and liver and kidney functions, in addition to gross and microscopic histological examination.

resultsSELP-815K analogues efficiently controlled the duration and extent of transfection in tumors for up to 5 weeks with no detectable spread to the liver. An approximately five-fold greater reduction in tumor volume was obtained with matrix-mediated delivery compared to intra-tumoral injection of adenoviruses in saline. SELP matrix proved safe in all injected mice compared to the control group.

conclusionsThe SELP-controlled gene delivery approach could potentially improve the anticancer activity of virus-mediated gene therapy at the same time as limiting viral spread to normal organs.

Indexed as

Genetic TherapyAdenoviridaeAnimalsBiopolymersHead and Neck NeoplasmsImaging, Three-DimensionalKidney Function TestsLiver Function TestsLuciferasesLuminescent MeasurementsMiceMice, NudeProdrugsRecombinant Fusion ProteinsThymidine KinaseTreatment OutcomeBiopolymersLuciferasesProdrugsRecombinant Fusion Proteinssilk-elastinlike protein 47KThymidine Kinase

Identifiers

PMID20603862
PMCPMC2906606
OpenAlexW2027672562

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.