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SHR Neuro Krebs Kardio Lipid

Madhusudhan, N; Pausan, MR; Halwachs, B; Durdević, M; Windisch, M; Kehrmann, J; Patra, V; Wolf, P; Boukamp, P; Moissl-Eichinger, C; Cerroni, L; Becker, JC; Gorkiewicz, G.
Molecular Profiling of Keratinocyte Skin Tumors Links Staphylococcus aureus Overabundance and Increased Human β-Defensin-2 Expression to Growth Promotion of Squamous Cell Carcinoma.
Cancers (Basel). 2020; 12(3): [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG


Autor/innen der Med Uni Graz:
Becker Jürgen Christian
Cerroni Lorenzo
Durdevic Marija
Gorkiewicz Gregor
Halwachs-Wenzl Bettina
Madhusudhan Nandhitha
Moissl-Eichinger Christine
Patra Vijaykumar
Pausan Manuela-Raluca
Windisch Markus
Wolf Peter

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Number of Figures: 6
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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 S. aureus, a specific induction of hBD-2 expression and increased tumor cell growth was seen. Increased proliferation was also induced by directly challenging SCC cells with hBD-2. Together, our data indicate that a changed microbial community composition in SCC, specified by S. aureus overabundance, might promote tumor cell growth via modulation of hBD-2 expression.

Find related publications in this database (Keywords)
skin microbiota
actinic keratosis
squamous cell carcinoma
basal cell carcinoma
Staphylococcus aureus
antimicrobial peptides
human beta-defensin
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