Lv Rui, Wang Danyan, Wang Tengyue, Li Rongqun, Zhuang Aiwen
School of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Zhuji Second People's Hospital, Zhuji, China.
Medicine (Baltimore). 2024 Dec 6;103(49):e40815. doi: 10.1097/MD.0000000000040815.
The association between gut microbiota (GM) and breast cancer (BC) has been studied. Nevertheless, the causal relationship between them and the potential mediating factors have not been clearly defined. Therefore, in this study, Mendelian randomization analysis (MR) was employed to explore the causal relationship between 473 GM and BC, as well as the mediating effect of potential immune cells. In this investigation, we availed ourselves of the publicly accessible summary statistics from the genome-wide association study to undertake two-sample and reverse Mendelian randomization analyses on GM and BC, with the intention of clarifying the causal association between GM and BC. Subsequently, through the application of the two-step Mendelian randomization analysis, it was revealed that the relationship between GM and BC was mediated by immune cells. The stability of the research outcomes was verified via sensitivity analysis. Mendelian randomization analysis elucidated the protective impacts of 8 genera on BC (such as Phylum Actinobacteriota, Species Bacteroides A plebeius A, Species Bifidobacterium adolescentis, Species CAG-841 sp002479075, Family Fibrobacteraceae, Order Fibrobacterales, Class Fibrobacteria, and Species Phascolarctobacterium sp003150755). Additionally, there are 23 immune cell traits related to BC. Our research findings showed that the species Megamonas funiformis was associated with an increased risk of BC, and 11.20% of this effect was mediated by CD38 on IgD+ CD24-. Likewise, HLA DR on CD33br HLA DR+ CD14- mediated the causal relationship between Species Prevotellamassilia and BC, having a mediating ratio of 7.89%. This study clarifies a potential causal relationship between GM, immune cells, and BC and provides genetic evidence for this causal connection. It offers research directions for the subsequent prevention and treatment of BC through the interaction between GM and immune cells, and provides a reference for future mechanistic and clinical studies in this field.
肠道微生物群(GM)与乳腺癌(BC)之间的关联已得到研究。然而,它们之间的因果关系以及潜在的中介因素尚未明确界定。因此,在本研究中,采用孟德尔随机化分析(MR)来探究473种GM与BC之间的因果关系,以及潜在免疫细胞的中介作用。在本次调查中,我们利用全基因组关联研究中公开可用的汇总统计数据,对GM和BC进行两样本和反向孟德尔随机化分析,旨在阐明GM与BC之间的因果关联。随后,通过应用两步孟德尔随机化分析,发现GM与BC之间的关系由免疫细胞介导。通过敏感性分析验证了研究结果的稳定性。孟德尔随机化分析阐明了8个属对BC的保护作用(如放线菌门、普通拟杆菌、青春双歧杆菌、CAG-841 sp002479075种、纤维杆菌科、纤维杆菌目、纤维杆菌纲和袋熊杆菌属sp003150755种)。此外,有23种免疫细胞特征与BC相关。我们的研究结果表明,梭形巨单胞菌与BC风险增加有关,其中11.20%的这种效应由IgD + CD24 - 上的CD38介导。同样,CD33br HLA DR + CD14 - 上的HLA DR介导了普雷沃氏菌属与BC之间的因果关系,中介比例为7.89%。本研究阐明了GM、免疫细胞与BC之间潜在的因果关系,并为这种因果联系提供了遗传学证据。它为后续通过GM与免疫细胞之间的相互作用预防和治疗BC提供了研究方向,并为该领域未来的机制和临床研究提供了参考。