Evidence map›Paper›PMID 23032977›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2013

Infectivity-selective oncolytic adenovirus developed by high-throughput screening of adenovirus-formatted library.

Yoshiaki Miura, Satoshi Yamasaki, Julia Davydova, Eric Brown, Kazunori Aoki, Selwyn Vickers, Masato Yamamoto

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

20 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Gene Therapy Leaves a Vicious Cycle.Frontiers in oncology · 2019
    Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Gene and virotherapy for hematological malignancies.International journal of hematology · 2016
    Review
  17. Oncolytic viruses: From bench to bedside with a focus on safety.Human vaccines & immunotherapeutics · 2015
    Review
  18. Review
  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.

Yoshiaki MiuraDivision of Basic and Translational Research, Department of Surgery, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Satoshi Yamasaki
Julia Davydova
Eric Brown
Kazunori Aoki
Selwyn Vickers
Masato Yamamoto
University of Minnesota · USUniversity of Minnesota Medical Center · US

Funding

UAB / UMN SPORE in Pancreatic CancerP50CA101955 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BUCHSBAUM, DONALD J · 2010 to 2014
$11.1M
Enhanced CRAd for Pancreatic CancerR01CA094084 · NCI · UNIVERSITY OF MINNESOTA · PI YAMAMOTO, MASATO · 2002 to 2013
$2.7M
Next Generation Oncolytic Adenovirus for Advanced Pancreatic Cancer TreatmentR01CA168448 · NCI · UNIVERSITY OF MINNESOTA · PI YAMAMOTO, MASATO · 2013 to 2017
$1.6M
NCI NIH HHS P50 CA101955NCI NIH HHS P50CA101955NCI NIH HHS R01 CA094084NCI NIH HHS R01 CA168448NCI NIH HHS R01CA168448NCI NIH HHS R01CA94084
6 · The paper itself

Abstract

Adenovirus (Ad) is a potent gene-delivery vehicle and has frequently been used for designing oncolytic viruses. However, lack of selectivity on infection has hampered the achievement of sufficient in vivo efficiency. Here, we developed a novel oncolytic virus system, infectivity-selective oncolytic adenovirus (ISOAd), via direct high-throughput screening of a high-diversity targeting-ligand library in adenoviral format. Through our newly designed rescue virus system, the high-diversity Ad library carrying the random seven amino acid sequences ligand-library in the AB-loop of its fiber-knob region (5 × 10(9) diversity) was successfully generated. During the screening of this library with the cells expressing the target molecule (mesothelin, MSLN), the AB-loop sequence of the virus clones converged to one dominant sequence and a novel MSLN-targeting sequence was isolated. The virus with the isolated motif showed selective infectivity to MSLN-positive cells in vitro. In vivo, it exhibited a selective and potent antitumor effect resulted from the viral replication in MSLN-positive xenografts. The ISOAd is a novel class of oncolytic Ad, which has selectivity at the step of transduction. The selectivity at the stage of infection can open new perspectives in oncolytic Ad therapy for various diseases.

Indexed as

Oncolytic VirotherapyAdenoviridaeAmino Acid SequenceAnimalsBase SequenceCell LineDNA PrimersFemaleFlow CytometryHumansMesothelinMiceMice, NudeMolecular Sequence DataPolymerase Chain ReactionVirulenceDNA PrimersMesothelinMSLN protein, humanMsln protein, mouse

Identifiers

PMID23032977
PMCPMC3538312
OpenAlexW2016714875

What OpenQuestion holds

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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.