Evidence map›Paper›PMID 24448161›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2014

A pRb-responsive, RGD-modified, and hyaluronidase-armed canine oncolytic adenovirus for application in veterinary oncology.

Eduardo Laborda, Cristina Puig-Saus, Alba Rodriguez-García, Rafael Moreno, Manel Cascalló, Josep Pastor, Ramon Alemany

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
3.0field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 44 citations in OpenAlex.

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  14. In vitro functional genetic modification of canine adenovirus type 2 genome by CRISPR/Cas9.Laboratory investigation; a journal of technical methods and pathology · 2021
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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

7 authors at 3 institutions in 1 country.

Eduardo Laborda1] Translational Research Laboratory, IDIBELL-Institut Català d'Oncologia, Barcelona, Spain [2] Biochemistry and Molecular Biology Department, Autonomous University of Barcelona, Barcelona, Spain.
Cristina Puig-SausTranslational Research Laboratory, IDIBELL-Institut Català d'Oncologia, Barcelona, Spain.
Alba Rodriguez-GarcíaTranslational Research Laboratory, IDIBELL-Institut Català d'Oncologia, Barcelona, Spain.
Rafael MorenoTranslational Research Laboratory, IDIBELL-Institut Català d'Oncologia, Barcelona, Spain.
Manel CascallóVCN Biosciences, Barcelona, Spain.
Josep PastorAnimal Medicine and Surgery Department, Fundació Hospital Clínic Veterinari, Autonomous University of Barcelona, Barcelona, Spain.
Ramon AlemanyTranslational Research Laboratory, IDIBELL-Institut Català d'Oncologia, Barcelona, Spain.
Institut d'Investigació Biomédica de Bellvitge · ESInstitut Català d'Oncologia · ESUniversitat Autònoma de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human and canine cancer share similarities such as genetic and molecular aspects, biological complexity, tumor epidemiology, and targeted therapeutic treatment. Lack of good animal models for human adenovirotherapy has spurred the use of canine adenovirus 2-based oncolytic viruses. We have constructed a canine oncolytic virus that mimics the characteristics of our previously published human adenovirus ICOVIR17: expression of E1a controlled by E2F sites, deletion of the pRb-binding site of E1a, insertion of an RGD integrin-binding motif at the fiber Knob, and expression of hyaluronidase under the major late promoter/IIIa protein splicing acceptor control. Preclinical studies showed selectivity, increased cytotoxicity, and strong hyaluronidase activity. Intratumoral treatment of canine osteosarcoma and melanoma xenografts in mice resulted in inhibition of tumor growth and prolonged survival. Moreover, we treated six dogs with different tumor types, including one adenoma, two osteosarcomas, one mastocitoma, one fibrosarcoma, and one neuroendocrine hepatic carcinoma. No virus-associated adverse effects were observed, but toxicity associated to tumor lysis, including disseminated intravascular coagulation and systemic failure, was found in one case. Two partial responses and two stable diseases warrant additional clinical testing.

Indexed as

Oncolytic VirotherapyAdenoviruses, CanineAnimalsDogsHumansHyaluronoglucosaminidaseMelanomaMiceOncolytic VirusesOsteosarcomaXenograft Model Antitumor AssaysHyaluronoglucosaminidase

Identifiers

PMID24448161
PMCPMC4015225
OpenAlexW2078835797

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.