Evidence map›Paper›PMID 41736367›Full record

ArticleJournal of microbiology (Seoul, Korea)2026

Preliminary characterization of the skin microbiota in basal cell carcinoma: An exploratory pilot study in Korean patients.

Hye Lim Keum, Woo Jun Sul, Suyeon Kim, In-Young Chung, Ara Koh, Hei Sung Kim

Abstract read
In one paragraph

Article in Journal of microbiology (Seoul, Korea), 2026. 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. Article
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

6 authors.

Hye Lim KeumSystems Microbial Ecology Laboratory, Department of Systems Biotechnology, Chung-Ang University, Anseong 17546, Republic of Korea.
Woo Jun SulSystems Microbial Ecology Laboratory, Department of Systems Biotechnology, Chung-Ang University, Anseong 17546, Republic of Korea.
Suyeon KimDepartment of Dermatology, Incheon St. Mary's Hospital, The Catholic University of Korea, Seoul 06591, Republic of Korea.
In-Young ChungDepartment of Life Sciences, POSTECH, Pohang 37673, Republic of Korea.
Ara KohDepartment of Life Sciences, POSTECH, Pohang 37673, Republic of Korea.
Hei Sung KimDepartment of Dermatology, Incheon St. Mary's Hospital, The Catholic University of Korea, Seoul 06591, Republic of Korea.

Funding

Catholic University of KoreaIncheon St. Mary's HospitalKorea Health Industry Development InstituteMinistry of Health and Welfare RS-2023-KH-136575Ministry of Health and Welfare RS-2025-02217860Ministry of Science and ICT 2023R1A2C1007759National Research Foundation of Korea
6 · The paper itself

Abstract

Basal cell carcinoma (BCC) is the most common form of skin cancer, with ultraviolet radiation recognized as the primary environmental driver; however, the potential contribution of alterations in the skin microbiota remains incompletely understood, particularly in Asian populations. This exploratory pilot study describes bacterial community patterns in BCC lesions compared with contralateral clinically normal skin in 20 Korean patients. Lesional and contralateral samples were obtained using paired skin swabs and punch biopsies and analyzed by full-length 16S rRNA gene sequencing, with targeted quantitative PCR (qPCR) of the roxP antioxidant gene of Cutibacterium acnes. Given the low-biomass nature of skin samples and the exploratory design, analyses focused on descriptive trends rather than confirmatory inference. Across available samples, C. acnes was the dominant taxon, with a trend toward lower relative abundance in BCC lesions, particularly in biopsy-derived datasets. Microbial evenness appeared higher in lesions than controls. Predictive functional profiling suggested reduced representation of vitamin B6 metabolism pathways in lesions, while qPCR analysis of swab samples showed a trend toward lower roxP/16S rRNA ratios in BCC-associated microbiota. These findings should be interpreted cautiously in light of methodological constraints, including sample heterogeneity, lidocaine exposure prior to biopsy, absence of sequencing-based negative controls, and reliance on predictive functional inference. Overall, this pilot study highlights potential differences in skin bacterial community structure between BCC lesions and contralateral skin in a Korean cohort. Larger, methodologically optimized studies incorporating metagenomic and functional validation will be required to determine whether these microbiota shifts contribute to, or result from, BCC-associated changes in the cutaneous environment.

Indexed as

BacteriaBasal Cell CarcinomaMicrobiotaSkinSkin MicrobiomeSkin NeoplasmsAgedBiopsyDNA, BacterialFemaleHumansMaleMiddle AgedPilot ProjectsRepublic of KoreaRNA, Ribosomal, 16SDNA, BacterialRNA, Ribosomal, 16Sbasal cell carcinomaKoreanskin microbiota

Identifiers

PMID41736367
PMCPMC13577125

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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.