Evidence map›Paper›PMID 34205379›Full record

ArticleCancers2021

Nectin-1 Expression Correlates with the Susceptibility of Malignant Melanoma to Oncolytic Herpes Simplex Virus In Vitro and In Vivo.

Barbara Schwertner, Georg Lindner, Camila Toledo Stauner, Elisa Klapproth, Clara Magnus, Anette Rohrhofer, Stefanie Gross, Beatrice Schuler-Thurner, Veronika Öttl, Nicole Feichtgruber and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
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  3. Identification of TPRA1 as a Novel Receptor and Predictive Biomarker for Oncolytic Virus M1.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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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

17 authors at 5 institutions in 1 country.

Barbara SchwertnerDepartment of Dermatology, University Hospital Regensburg, 93053 Regensburg, Germany.
Georg LindnerInstitute of Medical Microbiology and Hygiene, University of Regensburg, 93053 Regensburg, Germany.
Camila Toledo StaunerDepartment of Dermatology, University Hospital Regensburg, 93053 Regensburg, Germany.
Elisa KlapprothInstitute of Medical Microbiology and Hygiene, University of Regensburg, 93053 Regensburg, Germany.
Clara MagnusInstitute of Medical Microbiology and Hygiene, University of Regensburg, 93053 Regensburg, Germany.
Anette RohrhoferInstitute of Clinical Microbiology and Hygiene, University Hospital Regensburg, 93053 Regensburg, Germany.
Stefanie GrossDepartment of Dermatology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
Beatrice Schuler-ThurnerDepartment of Dermatology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.ORCID 0000-0001-8653-5425
Veronika ÖttlInstitute of Medical Microbiology and Hygiene, University of Regensburg, 93053 Regensburg, Germany.
Nicole FeichtgruberInstitute of Medical Microbiology and Hygiene, University of Regensburg, 93053 Regensburg, Germany.
Konstantin DrexlerDepartment of Dermatology, University Hospital Regensburg, 93053 Regensburg, Germany.
Katja EvertInstitute of Pathology, University of Regensburg, 93053 Regensburg, Germany.
Michael P KrahnMedical Cell Biology, Internal Medicine D, University Hospital Münster, 48149 Münster, Germany.
Mark BerneburgDepartment of Dermatology, University Hospital Regensburg, 93053 Regensburg, Germany.
Barbara SchmidtInstitute of Medical Microbiology and Hygiene, University of Regensburg, 93053 Regensburg, Germany.ORCID 0000-0003-0059-0349
Philipp SchusterInstitute of Medical Microbiology and Hygiene, University of Regensburg, 93053 Regensburg, Germany.
Sebastian HaferkampDepartment of Dermatology, University Hospital Regensburg, 93053 Regensburg, Germany.
University Hospital Regensburg · DEInstitute of Medical Microbiology and Hygiene · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversity Hospital Münster · DEUniversity of Regensburg · DE

Funding

Deutsche Forschungsgemeinschaft DFG HA 8481/1-1
6 · The paper itself

Abstract

Talimogene laherparepvec (T-VEC), an oncolytic herpes simplex virus, is approved for intralesional injection of unresectable stage IIIB/IVM1a melanoma. However, it is still unclear which parameter(s) predict treatment response or failure. Our study aimed at characterizing surface receptors Nectin-1 and the herpes virus entry mediator (HVEM) in addition to intracellular molecules cyclic GMP-AMP synthase (cGAS) and stimulator of interferon genes (STING) as potential bio-markers for oncolytic virus treatment. In 20 melanoma cell lines, oncolytic activity of T-VEC was correlated with the expression of Nectin-1 but not HVEM, as evaluated via flow cytometry and immunohistochemistry. Knockout using CRISPR/Cas9 technology confirmed the superior role of Nectin-1 over HVEM for entry and oncolytic activity of T-VEC. Neither cGAS nor STING as evaluated by Western Blot and immunohistochemistry correlated with T-VEC induced oncolysis. The role of these biomarkers was retrospectively analyzed for the response of 35 cutaneous melanoma metastases of 21 patients to intralesional T-VEC injection, with 21 (60.0%) of these lesions responding with complete (

Indexed as

herpes simplex virusmalignant melanomanectin-1oncolyticT-VEC

Identifiers

PMID34205379
PMCPMC8234279
OpenAlexW3174534096

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.