Evidence map›Paper›PMID 36765630›Full record

ArticleCancers2023

A20 as a Potential New Tool in Predicting Recurrence and Patient's Survival in Oral Squamous Cell Carcinoma.

Steffen Spoerl, Ramona Erber, Michael Gerken, Juergen Taxis, Nils Ludwig, Felix Nieberle, Niklas Biermann, Carol Immanuel Geppert, Tobias Ettl, Arndt Hartmann and 4 more

Abstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

14 authors.

Steffen SpoerlDepartment of Cranio-Maxillofacial Surgery, University Hospital Regensburg, 93053 Regensburg, Germany.
Ramona ErberInstitute of Pathology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Comprehensive Cancer Center Erlangen-EMN, 91054 Erlangen, Germany.ORCID 0000-0003-0315-1229
Michael GerkenTumor Center, Institute for Quality Management and Health Services Research, University of Regensburg, 93053 Regensburg, Germany.
Juergen TaxisDepartment of Cranio-Maxillofacial Surgery, University Hospital Regensburg, 93053 Regensburg, Germany.ORCID 0000-0002-9733-3703
Nils LudwigDepartment of Cranio-Maxillofacial Surgery, University Hospital Regensburg, 93053 Regensburg, Germany.ORCID 0000-0001-5561-2184
Felix NieberleDepartment of Cranio-Maxillofacial Surgery, University Hospital Regensburg, 93053 Regensburg, Germany.
Niklas BiermannDepartment of Plastic, Hand and Reconstructive Surgery, University Hospital Regensburg, 93053 Regensburg, Germany.
Carol Immanuel GeppertInstitute of Pathology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Comprehensive Cancer Center Erlangen-EMN, 91054 Erlangen, Germany.
Tobias EttlDepartment of Cranio-Maxillofacial Surgery, University Hospital Regensburg, 93053 Regensburg, Germany.
Arndt HartmannInstitute of Pathology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Comprehensive Cancer Center Erlangen-EMN, 91054 Erlangen, Germany.
Philipp BeckhoveDivision of Interventional Immunology, Leibniz Institute for Immunotherapy, 93053 Regensburg, Germany.
Torsten E ReichertDepartment of Cranio-Maxillofacial Surgery, University Hospital Regensburg, 93053 Regensburg, Germany.
Gerrit SpanierDepartment of Cranio-Maxillofacial Surgery, University Hospital Regensburg, 93053 Regensburg, Germany.ORCID 0000-0002-0226-7580
Silvia SpoerlDepartment of Internal Medicine 5-Haematology and Oncology, University Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A20, known as a potent inhibitor of NF-κB signaling, has been characterized in numerous clinical as well as preclinical studies. Recently, especially in various malignant diseases, the prognostic and therapeutic relevance of A20 was investigated. In oral squamous cell carcinoma (OSCC) however, the characterization of A20 is uncharted territory. We analyzed a tissue microarray (TMA) of 229 surgically-treated OSCC patients (2003-2013). Immunohistochemical (IHC) stainings were performed for A20 and CD3; additionally, standard haematoxylin-eosin staining was applied. IHC findings were correlated with a comprehensive dataset, comprising clinical and pathohistological information. A20 expression was analyzed in tumor cells as well as in tumor infiltrating lymphocytes (TILs) and correlated with the overall survival (OS) and recurrence-free survival (RFS) using uni- and multivariable Cox regression. The median follow-up time was 10.9 years and the A20 expression was significantly decreased in CD3+ TILs compared to mucosa-infiltrating lymphocytes (MILs). In the Kaplan-Meier analyses, higher A20 expression in TILs was correlated with better OS (

Indexed as

A20oral squamous cell carcinomaOSCCtissue microarrayTNFAIP3

Identifiers

PMID36765630
PMCPMC9913673

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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.