Evidence map›Paper›PMID 9524079›Full record

ArticleJournal of neuro-oncology1998

Adenovirus-mediated p53 gene delivery potentiates the radiation-induced growth inhibition of experimental brain tumors.

B Badie, M H Kramar, R Lau, D A Boothman, J S Economou, K L Black

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neuro-oncology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Oncolytic Viral Therapy for Malignant Glioma and Their Application in Clinical Practice.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    Review
  3. Review
  4. Review
  5. Current Approaches for Glioma Gene Therapy and Virotherapy.Frontiers in molecular neuroscience · 2021
    Review
  6. Article
  7. Gene therapy for malignant glioma.Molecular and cellular therapies · 2014
    Review
  8. Review
  9. Intelligent design: combination therapy with oncolytic viruses.Molecular therapy : the journal of the American Society of Gene Therapy · 2010
    Review
  10. Article
  11. Review
  12. Current and Future Gene Therapy for Malignant Gliomas.Journal of biomedicine & biotechnology · 2003
    Article
  13. Article
  14. Review
  15. The role of p53 in human cancer.Journal of neuro-oncology · 2001
    Review
  16. 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

6 authors at 4 institutions in 1 country.

B BadieDepartment of Neurological Surgery, University of Wisconsin, Madison 53792, USA.
M H Kramar
R Lau
D A Boothman
J S Economou
K L Black
University of California, Los Angeles · USNeurological Surgery · USUCLA Medical Center · USUniversity of Wisconsin–Madison · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
XIP8, AN X RAY INDUCIBLE KU70 BINDING PROTEINR01CA078530 · NCI · UNIVERSITY OF WISCONSIN MADISON · PI BOOTHMAN, DAVID A · 1998 to 2001
$433k
NCI NIH HHS CA-16042NCI NIH HHS R01 CA078530
6 · The paper itself

Abstract

Patients with malignant gliomas continue to have very poor prognosis even after surgical resection, radiation and chemotherapy. Because these tumors often have alterations in the p53 tumor suppressor gene, which plays a key role in the cellular response to DNA damaging agents, we investigated the role of p53 gene therapy in conjunction with ionizing radiation in a rat brain tumor model. Exposure of cultured rat 9L gliosarcoma cells, which contain a mutant p53 gene, to a recombinant adenovirus-vector bearing the wild-type p53 gene (Adp53), induced apoptosis within 24 hours. Although ionizing radiation had no additional effect on apoptosis within this time frame, it caused G1 arrest in non-apoptotic cells after Adp53 therapy. In contrast, wild-type 9L cells demonstrated little G1 arrest after X-irradiation. When animals bearing brain tumors were irradiated after intratumoral Adp53 injections, more than 85% reduction in tumor size was noted. Moreover, the group of rats receiving both radiation and Adp53 therapy had a significant increase in survival as compared to animals receiving either therapy alone. These results support the use of p53 gene therapy as an adjunct to radiation in treatment of malignant brain tumors.

Indexed as

Gene Transfer TechniquesRadiation Injuries, ExperimentalAdenoviridaeAnimalsBrain NeoplasmsCell CycleGliosarcomaHumansRatsTumor Cells, CulturedTumor Suppressor Protein p53Tumor Suppressor Protein p53

Identifiers

PMID9524079
OpenAlexW64698069

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.