Genetic causal relationship between gut microbiota and cutaneous melanoma: a two-sample Mendelian randomization study

• Published in: Melanoma research Vol. 34; no. 3; p. 225
• Main Authors: Wang, Peizhou, Liu, Tun, Zhang, Qingguo, Luo, Pan
• Format: Journal Article
• Language: English
• Published: England 01.06.2024
• Subjects: Gastrointestinal Microbiome; Humans; Melanoma - genetics; Melanoma - microbiology; Melanoma, Cutaneous Malignant; Mendelian Randomization Analysis; Skin Neoplasms - genetics; Skin Neoplasms - microbiology
• ISSN: 1473-5636
• DOI: 10.1097/CMR.0000000000000960

Currently, numerous studies suggest a potential association between the gut microbiota and the progression of melanoma. Hence, our objective was to examine the genetic impact of the gut microbiota on melanoma through the utilization of the Mendelian randomization (MR) approach. This research employed Bacteroides, Streptococcus, Proteobacteria, and Lachnospiraceae as exposure variables and cutaneous melanoma (CM) as the outcome in a two-sample MR analysis. In this MR research, the primary analytical approach was the random-effects inverse-variance weighting (IVW) model. Complementary methods included weighted median, MR Egger, and basic and weighted models. We assessed both heterogeneity and horizontal pleiotropy in our study, scrutinizing whether the analysis results were affected by any individual SNP. The random-effects IVW outcomes indicated that Streptococcus, Bacteroides, Lachnospiraceae and Proteobacteria had no causal relationship with CM, with odds ratios of 1.001 [95% confidence interval (CI) = 0.998-1.004, P  = 0.444], 0.999 (95% CI = 0.996-1.002, P  = 0.692), 1.001 (95% CI = 0.998-1.003, P  = 0.306), and 0.999 (95% CI = 0.997-1.002, P  = 0.998), respectively. No analyses exhibited heterogeneity, horizontal pleiotropy, or deviations. Our research determined that Bacteroides, Streptococcus, Proteobacteria, and Lachnospiraceae do not induce CM at the genetic level. However, we cannot dismiss the possibility that these four gut microbiotas might influence CM through other mechanisms.