Evidence map›Paper›PMID 19149629›Full record

ReviewCurrent stem cell research & therapy2009

Stem cells as vectors to deliver HSV/tk gene therapy for malignant gliomas.

Prakash Rath, Huidong Shi, Joel A Maruniak, N Scott Litofsky, Bernard L Maria, Mark D Kirk

Abstract readReview
In one paragraph

Review in Current stem cell research & therapy, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Nucleic acid drug vectors for diagnosis and treatment of brain diseases.Signal transduction and targeted therapy · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Genetically engineered theranostic mesenchymal stem cells for the evaluation of the anticancer efficacy of enzyme/prodrug systems.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Article
  10. Article
  11. Gene therapy for malignant glioma.Molecular and cellular therapies · 2014
    Review
  12. Systemic tumor-specific gene delivery.Journal of controlled release : official journal of the Controlled Release Society · 2013
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Neurotransplantation: lux et veritas, fiction or reality?Journal of neurosurgical sciences · 2011
    Review
  18. [Cutaneous mesenchymal stem cells. Current status of research and potential clinical applications].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2010
    Review
  19. Article
  20. 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

6 authors at 1 institution in 1 country.

Prakash RathDivision of Biological Sciences, University of Missouri-Columbia, Columbia, MO 65211, USA.
Huidong Shi
Joel A Maruniak
N Scott Litofsky
Bernard L Maria
Mark D Kirk
University of Missouri · US

Funding

Stem Cell Therapies For Batten DiseaseR01NS045813 · NINDS · UNIVERSITY OF MISSOURI-COLUMBIA · PI KIRK, MARK D · 2004 to 2007
$1.0M
NINDS NIH HHS NS 045813NINDS NIH HHS R01 NS045813
6 · The paper itself

Abstract

The prognosis of patients diagnosed with malignant gliomas including glioblastoma multiforme (GBM) is poor and there is an urgent need to develop and translate novel therapies into the clinic. Neural stem cells display remarkable tropism toward GBMs and thus may provide a platform to deliver oncolytic agents to improve survival. First we provide a brief review of clinical trials that have used intra-tumoral herpes simplex virus thymidine kinase (HSV/tk) gene therapy to treat brain tumors. Then, we review recent evidence that neural stem cells can be used to deliver HSV/tk to GBMs in animal models. While previous clinical trials used viruses or non-migratory vector-producing cells to deliver HSV/tk, the latter approaches were not effective in humans, primarily because of satellite tumor cells that escaped surgical resection and survived due to low efficiency delivery of HSV/tk. To enhance delivery of HSV/tk to kill gliomas cells, recent animal studies have focused on the ability of neural stem cells, transduced with HSV/tk, to migrate efficiently and selectively to regions occupied by GBM cells. This approach holds the promise of targeting GBM cells that have infiltrated the brain well beyond the original site of the tumor epicenter.

Indexed as

Stem Cell TransplantationTransduction, GeneticAnimalsAntineoplastic AgentsCell MovementClinical Trials as TopicGenetic TherapyGlioblastomaHumansNeoplasm MetastasisNeoplasms, ExperimentalNeuronsOncolytic VirotherapySimplexvirusThymidine KinaseViral ProteinsAntineoplastic AgentsThymidine KinaseViral Proteins

Identifiers

PMID19149629
PMCPMC3384546
OpenAlexW2161612641

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.