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Record W2264651442

Systemic administration of mutant vesicular stomatitis virus (VSV) completely eradicates nasopharyngeal carcinoma (NPC) models

2006· article· en· W2264651442 on OpenAlexaff
Nehad M. Alajez, Joseph D. Mocanu, Shane Knowles, John C. Bell, Fei‐Fei Liu

Bibliographic record

VenueCancer Research · 2006
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicVirus-based gene therapy research
Canadian institutionsOntario Institute for Cancer Research
Fundersnot available
KeywordsVesicular stomatitis virusNasopharyngeal carcinomaCytotoxic T cellVirologyBiologyApoptosisMultiplicity of infectionIn vivoCancer researchIn vitroMolecular biologyVirusMedicineRadiation therapyInternal medicine
DOInot available

Abstract

fetched live from OpenAlex

Proc Amer Assoc Cancer Res, Volume 47, 2006 2177 Introduction: Nasopharyngeal carcinoma (NPC) is a malignancy of the head and neck region with unique clinical and demographic features. Standard therapy for NPC achieves only modest survival rates, underscoring a need to develop novel therapies. Our group has previously investigated multiple novel molecular therapeutics including adenoviral vectors, and antisense oligonucleotide approaches. None has succeeded in complete eradication of established xenograft tumours. Hence, we were interested in examining the therapeutic potential of vesicular stomatitis viruses (VSV), which preferentially replicate in malignant cells, presumably due to defects in their interferon (IFN) signaling. Materials and Methods: Two EBV-positive human NPC models were utilized: the C666-1, and the C17 tumours. The MTS assay was utilized to assess viability in vitro ; apoptosis was measured using flow-based techniques including fraction of cells in the sub-G0/G1 phase, and caspase-3 activation. In vivo experiments were conducted using nu/nu mice, which are permissive to VSV infection. The VSV-delta51-GFP is a mutant VSV carrying the GFP reporter gene; control VSV was inactivated by UV radiation (30 min in laminar flow hood). Results: Our data demonstrated that VSV-delta51-GFP (MOI = 0.00001 to 10.0) was cytotoxic to C666-1 cells in a time and dose-dependent manner (75.4 to 87.2 killing at 72 hrs, respectively). Control VSV demonstrated no cytotoxicity. VSVdelta51 infection of C666-1 cells at MOI=1.0 induced apoptosis in > 6.2% of infected cells at 24 hrs and reached >10.8 % at 72 hrs. C666-1 cells (5x10^6) infected ex vivo with VSVdelta51-GFP (MOI=5.0) and then implanted into nu/nu mice demonstrated no tumour formation when injected subcutaneously, followed for 58 days, while C666-1 cells infected with UV-irradiated control virus formed tumors as early as day 27 post injection. Therapeutic efficacy of VSVdelta51-GFP was evaluated in both the C666-1 and C17 models. Four intravenous injections of VSVdelta51-GFP (5x1^8 pfu x 4) were able to completely eradicate established tumours followed for 31 days. No adverse effects were observed in mice treated with VSV; control VSV demonstrated no in vivo effect. Conclusion: These data demonstrate that VSV is a potentially promising novel oncolytic viral therapeutic modality for NPC. We are currently investigating the therapeutic benefit of combining VSV with RT and chemotherapy, and anticipate application to human patients in the near future if the combinatorial strategy demonstrates such impressive efficacy. Our finding may also be applicable to other human cancers.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.005

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0020.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.056
GPT teacher head0.354
Teacher spread0.298 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2006
Admission routes1
Has abstractyes

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