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. 2025 Apr 25;13(5):992.
doi: 10.3390/microorganisms13050992.

Investigating Skin Microbial Community in Malignant Melanoma Lesions

Affiliations

Investigating Skin Microbial Community in Malignant Melanoma Lesions

Michele Properzi et al. Microorganisms. .

Abstract

The skin microbiome is identified as one of the crucial factors in several pathological conditions, including its potential capacity in modulating cancer progression and response to treatment. A strong association of Bacilli and Betaproteobacteria classes and the Bacteroidetes phylum with melanoma is described in patients with cutaneous malignancies, while an imbalance of S. epidermidis and S. aureus is related to the progression of other skin cancers. In the present study, we characterized the microbial community in suspected lesions of 35 patients, classified, after histological analysis, as malignant melanoma lesions and benign non-melanoma lesions. Mirrored healthy skin were also included as negative control. No significant difference in alpha and beta diversity was observed when samples were categorized in four different groups (melanoma samples vs. contralateral healthy samples; melanoma samples vs. benign lesions; benign lesions vs. contralateral controls; melanoma controls vs. benign controls). The differential abundance analyses show that Corynebacterium urealyticum is more abundant in melanoma samples compared to their control, while Roseomonas gilardii is less abundant in melanoma. Staphylococcus massiliensis, Bacillus coagulans, Paracoccus yeei, Corynebacterium jeikeium, and Corynebacterium pyruviciproducens are present only in melanoma samples when compared with benign lesions.

Keywords: benign skin lesion; biomarker; melanoma; skin microbiota.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
(A) Distribution of reads depth. (B) Rarefaction curve; the curves represent the following: purple = M-Samp, blue = M-Ctrl, green = B-Samp, red = B-Ctrl. (C) Phylogenetic tree representing all the species found in the samples, distinguished by phylum and abundance.
Figure 2
Figure 2
(A) Boxplots of alpha diversity by Shannon metric. (B) Bray–Curtis graph for beta diversity. (C) Heatmap showing the abundance levels of each species with significant differential abundance for the four comparisons evaluated. In the heatmap, fold change indicates differential abundance of the species. Specifically: (1) In the M-Samp vs. M-Ctrl column, positive fold change indicates higher abundance in M-Samp; (2) In the M-Samp vs. B-Samp column, positive fold change indicates higher abundance in M-Samp; (3) In the B-Samp vs. B-Ctrl column, positive fold change indicates higher abundance in B-Samp; (4) In the M-Ctrl vs. B-Ctrl column, positive fold change indicates higher abundance in M-Ctrl. “ns” means “not significant”.

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