Evidence map›Paper›PMID 26900598›Full record

ArticleMolecular therapy oncolytics

Evaluation of polymer shielding for adenovirus serotype 6 (Ad6) for systemic virotherapy against human prostate cancers.

Tien V Nguyen, Greg J Heller, Mary E Barry, Catherine M Crosby, Mallory A Turner, Michael A Barry

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy oncolytics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.0field-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

17 citing papers in PubMed, 27 citations in OpenAlex.

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  5. Strategies for Modifying Adenoviral Vectors for Gene Therapy.International journal of molecular sciences · 2024
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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.

Tien V NguyenDepartment of Internal Medicine, Division of Infectious Diseases, Translational Immunovirology and Biodefense Program, Rochester, Minnesota, USA.
Greg J HellerPostbaccalaureate Research Education Program, Rochester, Minnesota, USA.
Mary E BarryDepartment of Internal Medicine, Division of Infectious Diseases, Translational Immunovirology and Biodefense Program, Rochester, Minnesota, USA.
Catherine M CrosbyVirology and Gene Therapy Graduate Program, Rochester, Minnesota, USA.
Mallory A TurnerVirology and Gene Therapy Graduate Program, Rochester, Minnesota, USA.
Michael A BarryDepartment of Internal Medicine, Division of Infectious Diseases, Translational Immunovirology and Biodefense Program, Rochester, Minnesota, USA; Department of Immunology, Rochester, Minnesota, USA; Department of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
University of Minnesota Rochester · US

Funding

TRAINING IN TRANSLATIONAL RESEARCH: BENCH TO BEDSIDER25GM055252 · NIGMS · MAYO CLINIC ROCHESTER · PI LUJAN, LUIS, MAHER, LOUIS JAMES · 1996 to 2022
$8.3M
Post-baccalaureate Training in Biomedical ResearchR25GM075148 · NIGMS · MAYO CLINIC ROCHESTER · PI LUJAN, LUIS, MAHER, LOUIS JAMES · 2006 to 2024
$6.1M
Improving the Pharmacology of Oncolytic AdenovirusR01CA136945 · NCI · MAYO CLINIC ROCHESTER · PI BARRY, MICHAEL A · 2010 to 2014
$1.5M
NCI NIH HHS R01 CA136945NIGMS NIH HHS R25 GM055252NIGMS NIH HHS R25 GM075148
6 · The paper itself

Abstract

Oncolytic viruses hold promise as "self-amplifying" cancer therapies wherein a virally killed cell can produce thousands of new viral "drugs" that can kill more cancer cells. Adenoviruses (Ads) are one family of oncolytic viruses. Most human studies have used human Ad serotype 5 (Ad5). Unfortunately, most patients are already immune to Ad5 increasing the likelihood that the agent will be neutralized if used as a cancer therapy. In this work, lower seroprevalence Ad6 was tested as a systemic therapy for prostate cancer. Ad5 and Ad6 were injected intravenously a single time in nude mice bearing human prostate tumors, and toxicity and efficacy were assessed. Ad6 was chemically shielded with polyethylene glycol (PEG) to test if this would further improve its pharmacology. Ad6 produced 30-fold lower liver damage and less toxicity than Ad5. Ad6 significantly repressed the growth of androgen-resistant human DU145 prostate tumors and androgen-sensitive LNCaP tumors after single intravenous injection. PEGylation did not change virus distribution, but blunted liver damage and cytokine production by Ad6. PEGylated Ad6 eradicated LNCaP tumors and maintained body mass, but lost potency against the more challenging DU145 tumors. These and other data suggest that low seroprevalent Ad6 has better efficacy and safety than the benchmark oncolytic virus Ad5 for systemic therapy of prostate cancer. These data also indicate that PEGylation may improve Ad6 safety, but that this shielding may reduce oncolytic efficacy after intravenous treatment.

Identifiers

PMID26900598
PMCPMC4758940
OpenAlexW2411313245

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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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.