Evidence map›Paper›PMID 16871231›Full record

ArticleGene therapy2006

Imaging immediate-early and strict-late promoter activity during oncolytic herpes simplex virus type 1 infection and replication in tumors.

S Yamamoto, L A Deckter, K Kasai, E A Chiocca, Y Saeki

Abstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. NOTCH-Induced MDSC Recruitment after oHSV Virotherapy in CNS Cancer Models Modulates Antitumor Immunotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  3. Toxicity and Efficacy of a Novel GADD34-expressing Oncolytic HSV-1 for the Treatment of Experimental Glioblastoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  4. Article
  5. Review
  6. Article
  7. Multimechanistic tumor targeted oncolytic virus overcomes resistance in brain tumors.Molecular therapy : the journal of the American Society of Gene Therapy · 2013
    Article
  8. Article
  9. Article
  10. HSV Recombinant Vectors for Gene Therapy.The open virology journal · 2010
    Article
  11. Article
  12. Designing Herpes Viruses as Oncolytics.Molecular therapy oncolytics
    Article
  13. 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

5 authors at 2 institutions in 2 countries.

S YamamotoDardinger Laboratory for Neuro-oncology and Neurosciences, Department of Neurological Surgery, James Cancer Hospital and Solove Research Institute, The Ohio State University Medical Center, Columbus, OH, USA.
L A Deckter
K Kasai
E A Chiocca
Y Saeki
The Ohio State University · USThe Ohio State University Wexner Medical Center · US

Funding

The role of microvesicles in giloma virotherapyP01CA069246 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI CHAREST, ALAIN · 1996 to 2021
$30.9M
Interdisciplinary Tumor Complexity ModelingR01CA085139 · NCI · OHIO STATE UNIVERSITY · PI CHIOCCA, E. ANTONIO · 2003 to 2006
$4.0M
HSV Amplicon Vectors for Cerebral IschemiaR01NS041571 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI CHIOCCA, E. ANTONIO · 2002 to 2004
$1.2M
NCI NIH HHS P01 CA69246NCI NIH HHS R01 CA85139NINDS NIH HHS R01 NS41571
6 · The paper itself

Abstract

An increasing number of oncolytic viruses have been developed and studied for cancer therapy. In response to needs for non-invasive monitoring and imaging of oncolytic virotherapy, several different approaches, including a positron emission tomography-based method, a method using secreted marker peptides, and optical imaging-based methods, have been reported. Among these modalities, we utilized the luciferase-based bioluminescent assay/imaging systems to determine the kinetics and dynamics of a productive viral infection. The replication cycle of herpes simplex virus type 1 (HSV-1) is punctuated by a temporal cascade of three classes of viral genes: immediate-early (IE), early (E) and late (L) genes. U(L)39- and gamma(1)34.5-deleted, replication-conditional HSV-1 mutants that express firefly luciferase under the control of the IE4/5 or strict-late gC promoters were generated. These oncolytic viruses were examined in cultured cells and a mouse tumor model. IE promoter- and strict-late promoter-mediated luciferase expression was confirmed to indicate viral infection and replication, respectively. Incorporation of a strict-late promoter-driven luciferase cassette into oncolytic HSV-1 vectors would be useful for assessing tumor oncolysis in preclinical tumor treatment studies.

Indexed as

Promoter Regions, GeneticAnimalsAntiviral AgentsCell LineChlorocebus aethiopsGene ExpressionGenetic EngineeringGenetic TherapyGenetic VectorsHerpes SimplexHerpesvirus 1, HumanHumansLuciferasesLuminescent ProteinsMiceMice, NudeAntiviral AgentsLuciferasesLuminescent ProteinsPhosphonoacetic AcidPurinesRoscovitine

Identifiers

PMID16871231
OpenAlexW2078993865

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.