Evidence map›Paper›PMID 27119113›Full record

ArticleMolecular therapy oncolytics2016

Development of new therapy for canine mammary cancer with recombinant measles virus.

Koichiro Shoji, Misako Yoneda, Tomoko Fujiyuki, Yosuke Amagai, Akane Tanaka, Akira Matsuda, Kikumi Ogihara, Yuko Naya, Fusako Ikeda, Hiroshi Matsuda and 2 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy oncolytics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

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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

12 authors at 4 institutions in 1 country.

Koichiro ShojiLaboratory Animal Research Center, Institute of Medical Science, University of Tokyo , Japan.
Misako YonedaLaboratory Animal Research Center, Institute of Medical Science, University of Tokyo , Japan.
Tomoko FujiyukiLaboratory Animal Research Center, Institute of Medical Science, University of Tokyo , Japan.
Yosuke AmagaiLaboratory Animal Research Center, Institute of Medical Science, University of Tokyo , Japan.
Akane TanakaLaboratories of Comparative Animal Medicine, Division of Animal Life Science, Tokyo University of Agriculture and Technology , Japan.
Akira MatsudaLaboratories of Veterinary Molecular Pathology and Therapeutics, Division of Animal Life Science, Tokyo University of Agriculture and Technology , Japan.
Kikumi OgiharaDepartment of Pathology, School of Life and Environmental Science, Azabu University , Japan.
Yuko NayaDepartment of Pathology, School of Life and Environmental Science, Azabu University , Japan.
Fusako IkedaLaboratory Animal Research Center, Institute of Medical Science, University of Tokyo , Japan.
Hiroshi MatsudaLaboratories of Veterinary Molecular Pathology and Therapeutics, Division of Animal Life Science, Tokyo University of Agriculture and Technology , Japan.
Hiroki SatoLaboratory Animal Research Center, Institute of Medical Science, University of Tokyo , Japan.
Chieko KaiLaboratory Animal Research Center, Institute of Medical Science, University of Tokyo , Japan.
Tokyo University of Science · JPTokyo University of Agriculture and Technology · JPAzabu University · JPThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oncolytic virotherapy is a promising treatment strategy for cancer. We previously generated a recombinant measles virus (rMV-SLAMblind) that selectively uses a poliovirus receptor-related 4 (PVRL4/Nectin4) receptor, but not signaling lymphocyte activation molecule (SLAM). We demonstrated that the virus exerts therapeutic effects against human breast cancer cells. Here, we examined the applicability of rMV-SLAMblind to treating canine mammary cancers (CMCs). We found that the susceptibilities of host cells to rMV-SLAMblind were dependent on canine Nectin-4 expression. Nectin-4 was detected in four of nine CMC cell lines. The rMV-SLAMblind efficiently infected those four Nectin-4-positive cell lines and was cytotoxic for three of them (CF33, CHMm, and CTBm). In vivo experiment showed that the administration of rMV-SLAMblind greatly suppressed the progression of tumors in mice xenografted with a CMC cell line (CF33). Immunohistochemistry revealed that canine Nectin-4 was expressed in 45% of canine mammary tumors, and the tumor cells derived from one clinical specimen were efficiently infected with rMV-SLAMblind. These results suggest that rMV-SLAMblind infects CMC cells and displays antitumor activity in vitro, in xenografts, and ex vivo. Therefore, oncolytic virotherapy with rMV-SLAMblind can be a novel method for treating CMCs.

Identifiers

PMID27119113
PMCPMC4782952
OpenAlexW2233239467

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.