Evidence map›Paper›PMID 32111012›Full record

ArticleCancers2020

Molecular Profiling of Keratinocyte Skin Tumors Links

Nandhitha Madhusudhan, Manuela R Pausan, Bettina Halwachs, Marija Durdević, Markus Windisch, Jan Kehrmann, VijayKumar Patra, Peter Wolf, Petra Boukamp, Christine Moissl-Eichinger and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 70 citations in OpenAlex.

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  13. Control of Methicillin-ResistantMicroorganisms · 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

13 authors at 4 institutions in 2 countries.

Nandhitha MadhusudhanInstitute of Pathology, Medical University of Graz, Neue Stiftingtalstrasse 6, 8010 Graz, Austria.
Manuela R PausanDepartment of Internal Medicine, Medical University of Graz, Auenbruggerplatz 15, 8036 Graz, Austria.
Bettina HalwachsInstitute of Pathology, Medical University of Graz, Neue Stiftingtalstrasse 6, 8010 Graz, Austria.
Marija DurdevićInstitute of Pathology, Medical University of Graz, Neue Stiftingtalstrasse 6, 8010 Graz, Austria.
Markus WindischInstitute of Pathology, Medical University of Graz, Neue Stiftingtalstrasse 6, 8010 Graz, Austria.
Jan KehrmannInstitute of Medical Microbiology, University Hospital Essen, University of Duisburg-Essen, Hufelandstrasse 55, 45122 Essen, Germany.
VijayKumar PatraDepartment of Dermatology, Medical University of Graz, Auenbruggerplatz 8, 8036 Graz, Austria.
Peter WolfDepartment of Dermatology, Medical University of Graz, Auenbruggerplatz 8, 8036 Graz, Austria.
Petra BoukampLeibniz Research Institute for Environmental Medicine, Auf'm Hennekamp 50, 40225 Düsseldorf, Germany.
Christine Moissl-EichingerDepartment of Internal Medicine, Medical University of Graz, Auenbruggerplatz 15, 8036 Graz, Austria.
Lorenzo CerroniDepartment of Dermatology, Medical University of Graz, Auenbruggerplatz 8, 8036 Graz, Austria.
Jürgen C BeckerDepartment of Translational Skin Cancer Research and Department of Dermatology, German Cancer Consortium (DKTK), University Hospital Essen, Universitätsstrasse 1, 45141 Essen, Germany.
Gregor GorkiewiczInstitute of Pathology, Medical University of Graz, Neue Stiftingtalstrasse 6, 8010 Graz, Austria.
Medical University of Graz · ATDeutschen Konsortium für Translationale Krebsforschung · DELeibniz Institute of Environmental Medicine · DEUniversity of Duisburg-Essen · DE

Funding

Austrian Science Fund FWF W1241-B18
6 · The paper itself

Abstract

The skin microbiota plays a prominent role in health and disease; however, its contribution to skin tumorigenesis is not well understood. We comparatively assessed the microbial community compositions from excision specimens of the main human non-melanoma skin cancers, actinic keratosis (AK), squamous cell carcinoma (SCC) and basal cell carcinoma (BCC). Keratinocyte skin tumors are characterized by significantly different microbial community compositions, wherein AK and SCC are more similar to each other than to BCC. Notably, in SCC, which represents the advanced tumor entity and frequently develops from AK, overabundance of Staphylococcus aureus, a known skin pathogen, was noted. Moreover, S. aureus overabundance was significantly associated with increased human β-defensin-2 (hBD-2) expression in SCC. By challenging human SCC cell lines with

Indexed as

actinic keratosisantimicrobial peptidesbasal cell carcinomahuman β-defensinskin microbiotasquamous cell carcinomaStaphylococcus aureus

Identifiers

PMID32111012
PMCPMC7139500
OpenAlexW3007236503

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.