Evidence map›Paper›PMID 16248789›Full record

ReviewCurrent topics in medicinal chemistry2005

Combining cytotoxic and immune-mediated gene therapy to treat brain tumors.

James F Curtin, Gwendalyn D King, Marianela Candolfi, Remy B Greeno, Kurt M Kroeger, Pedro R Lowenstein, Maria G Castro

Open access · greenAbstract readReview
In one paragraph

Review in Current topics in medicinal chemistry, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

27 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Emerging immunotherapies for glioblastoma.Expert opinion on emerging drugs · 2016
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
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  12. Article
  13. Review
  14. Opuntia humifusa partitioned extracts inhibit the growth of U87MG human glioblastoma cells.Plant foods for human nutrition (Dordrecht, Netherlands) · 2010
    Article
  15. Article
  16. Article
  17. Article
  18. Release of HMGB1 in response to proapoptotic glioma killing strategies: efficacy and neurotoxicity.Clinical cancer research : an official journal of the American Association for Cancer Research · 2009
    Article
  19. Article
  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

7 authors at 2 institutions in 1 country.

James F CurtinGene Therapeutics Research Institute, Cedars-Sinai Medical Center, Research Pavilion, Suite 5090, 8700 Beverly Boulevard, Los Angeles, CA 90048, USA.
Gwendalyn D King
Marianela Candolfi
Remy B Greeno
Kurt M Kroeger
Pedro R Lowenstein
Maria G Castro
Cedars-Sinai Medical Center · USUniversity of California, Los Angeles · US

Funding

Trophic gene transfer in MPTP animalsU54NS045309 · NINDS · UNIVERSITY OF ROCHESTER · PI FEDEROFF, HOWARD J. · 2002 to 2006
$9.7M
Gene therapy for chronic neurodegenerative disordersR01NS044556 · NINDS · CEDARS-SINAI MEDICAL CENTER · PI CASTRO, MARIA G · 2002 to 2006
$2.0M
Gene Therapy for Neurological DiseasesR01NS042893 · NINDS · CEDARS-SINAI MEDICAL CENTER · PI LOWENSTEIN, PEDRO R · 2002 to 2006
$1.8M
Gene Therapy for GliomaR21NS047298 · NINDS · CEDARS-SINAI MEDICAL CENTER · PI LOWENSTEIN, PEDRO R · 2003 to 2004
$354k
APOPTOSIS OF ANTERIOR PITUITARY CELLSR03TW006273 · FIC · CEDARS-SINAI MEDICAL CENTER · PI CASTRO, MARIA G · 2004 to 2006
$102k
FIC NIH HHS 1R03 TW006273-01FIC NIH HHS R03 TW006273NINDS NIH HHS 1R01 NS42893-01NINDS NIH HHS 1R01 NS44556-01NINDS NIH HHS 1R21 NS047298-01NINDS NIH HHS R01 NS042893NINDS NIH HHS R01 NS044556NINDS NIH HHS R21 NS047298NINDS NIH HHS U54 NS045309NINDS NIH HHS U54 NS045309-01
6 · The paper itself

Abstract

Glioblastoma (GBM) is a type of intracranial brain tumor, for which there is no cure. In spite of advances in surgery, chemotherapy and radiotherapy, patients die within a year of diagnosis. Therefore, there is a critical need to develop novel therapeutic approaches for this disease. Gene therapy, which is the use of genes or other nucleic acids as drugs, is a powerful new treatment strategy which can be developed to treat GBM. Several treatment modalities are amenable for gene therapy implementation, e.g. conditional cytotoxic approaches, targeted delivery of toxins into the tumor mass, immune stimulatory strategies, and these will all be the focus of this review. Both conditional cytotoxicity and targeted toxin mediated tumor death, are aimed at eliminating an established tumor mass and preventing further growth. Tumors employ several defensive strategies that suppress and inhibit anti-tumor immune responses. A better understanding of the mechanisms involved in eliciting anti-tumor immune responses has identified promising targets for immunotherapy. Immunotherapy is designed to aid the immune system to recognize and destroy tumor cells in order to eliminate the tumor burden. Also, immune-therapeutic strategies have the added advantage that an activated immune system has the capability of recognizing tumor cells at distant sites from the primary tumor, therefore targeting metastasis distant from the primary tumor locale. Pre-clinical models and clinical trials have demonstrated that in spite of their location within the central nervous system (CNS), a tissue described as 'immune privileged', brain tumors can be effectively targeted by the activated immune system following various immunotherapeutic strategies. This review will highlight recent advances in brain tumor immunotherapy, with particular emphasis on advances made using gene therapy strategies, as well as reviewing other novel therapies that can be used in combination with immunotherapy. Another important aspect of implementing gene therapy in the clinical arena is to be able to image the targeting of the therapeutics to the tumors, treatment effectiveness and progression of disease. We have therefore reviewed the most exciting non-invasive, in vivo imaging techniques which can be used in combination with gene therapy to monitor therapeutic efficacy over time.

Indexed as

Genetic TherapyImmunotherapyAntineoplastic AgentsBrain NeoplasmsCombined Modality TherapyDisease ProgressionGlioblastomaHumansInterferonsInterleukinsMagnetic Resonance ImagingPositron-Emission TomographyToxins, BiologicalAntineoplastic AgentsInterferonsInterleukinsToxins, Biological

Identifiers

PMID16248789
PMCPMC1629031
OpenAlexW2122526949

What OpenQuestion holds

Textmetadata
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.