Evidence map›Paper›PMID 27993141›Full record

ArticleJournal of translational medicine2016

Colonization of xenograft tumors by oncolytic vaccinia virus (VACV) results in enhanced tumor killing due to the involvement of myeloid cells.

Mehmet Okyay Kilinc, Klaas Ehrig, Maysam Pessian, Boris R Minev, Aladar A Szalay

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 35% 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

8 citing papers in PubMed, 9 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

5 authors at 3 institutions in 2 countries.

Mehmet Okyay KilincDepartment of Biochemistry, Biocenter, University of Würzburg, Am Hubland, 97074, Würzburg, Germany.
Klaas EhrigDepartment of Biochemistry, Biocenter, University of Würzburg, Am Hubland, 97074, Würzburg, Germany.
Maysam PessianSan Diego Science Center, Genelux Corporation, San Diego, CA, USA.
Boris R MinevSan Diego Science Center, Genelux Corporation, San Diego, CA, USA.
Aladar A SzalayDepartment of Biochemistry, Biocenter, University of Würzburg, Am Hubland, 97074, Würzburg, Germany. aladar.szalay@virchow.uni-wuerzburg.de.
Fleet Science Center · USUniversity of Würzburg · DEGenelux (United States) · US

Funding

Optimizing Induction Conditions for Immunotherapeutic CTLR01CA154256 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PRINS, ROBERT M · 2010 to 2014
$1.9M
NCI NIH HHS R01 CA154256
6 · The paper itself

Abstract

backgroundThe mechanisms by which vaccinia virus (VACV) interacts with the innate immune components are complex and involve different mechanisms. iNOS-mediated NO production by myeloid cells is one of the central antiviral mechanisms and this study aims to investigate specifically whether iNOS-mediated NO production by myeloid cells, is involved in tumor eradication following the virus treatment.

methodsHuman colon adenocarcinoma (HCT-116) xenograft tumors were infected by VACV. Infiltration of iNOS

resultsInfection of human colon adenocarcinoma (HCT-116) xenograft tumors by VACV has led to recruitment of many CD11b

conclusionsWe initially hypothesized that NO could be one of the factors that limits active spreading of the virus in the cancerous tissue. In contrast to our initial hypothesis, we observed that PMN-MDSCs were the main producer of NO through iNOS and NO provided a beneficial antitumor effect, The results strongly support an important novel role for VACV infection in the tumor microenvironment. VACV convert tumor-promoting MDSCs into tumor-killing cells by inducing higher NO production.

Indexed as

Cytotoxicity, ImmunologicXenograft Model Antitumor AssaysAnimalsCell ProliferationHCT116 CellsHumansKineticsMaleMice, NudeMyeloid CellsNeutrophilsNitric OxideNitric Oxide Synthase Type IIOncolytic VirusesTumor BurdenVaccinia virusNitric OxideNitric Oxide Synthase Type IIAntitumor immune responseAntiviral immunityInnate immune systemiNOSMDSCsNOOncolytic virus therapyVACV

Identifiers

PMID27993141
PMCPMC5168712
OpenAlexW2561073572

What OpenQuestion holds

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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.