{"title":"鼻咽部恶性肿瘤中肠道微生物-免疫细胞相互作用的孟德尔随机分析。","authors":"Qicong Chen, Gang Wang, Jingcheng Shu, Xiaosu Zou, Weiwei Miao, Wenqian Nong, Min Li, Guiping Lan, Wenlin Huang, Xueying Huang, Honglin Luo, Shenhong Qu","doi":"10.1186/s13568-025-01909-2","DOIUrl":null,"url":null,"abstract":"<p><p>Observational studies have suggested associations among the gut microbiome, immune cells, and the risk of malignant neoplasms of nasopharynx. However, the causality of these relationships remains unclear. Thus, we conducted multiple Mendelian Randomization analyses to estimate the causal association of gut microbiota with the risk of malignant neoplasms of nasopharynx and to evaluate the mediating effect of immune cells on this causal pathway. Genetic variants extracted from genome-wide association studies of human gut microbiota compositions (n = 211), immune cell traits (n = 731) and malignant neoplasms of nasopharynx served as instrumental variables for calculating causal associations and mediating effects. Four gut microbiota compositions and eight immune cell traits exhibited detrimental causal effects, while three gut microbiota compositions and fifteen immune cell traits demonstrated protective effects. Interestingly, the causal association of genus Candidatus Soleaferrea id.11350 was no longer significant after adjusting for two established immune cell traits (HLA DR + + monocyte %leukocyte and HLA DR + + monocyte % monocyte). Moreover, HLA DR + + monocyte %leukocyte exhibited a mediating effect (OR 0.75, 95% CI 0.59-0.96) on the causal pathway of genus Candidatus Soleaferrea id.11350-malignant neoplasms of nasopharynx, with a mediating proportion of 21.59%. To our knowledge, this study is the first to identify potential therapeutic targets and elucidate mechanistic insights for malignant neoplasms of nasopharynx interventions involving gut microbiota and immune cell traits; however, these findings warrant further validation through adequately powered randomized clinical trials (RCTs).</p>","PeriodicalId":7537,"journal":{"name":"AMB Express","volume":"15 1","pages":"106"},"PeriodicalIF":3.7000,"publicationDate":"2025-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12263519/pdf/","citationCount":"0","resultStr":"{\"title\":\"Mendelian randomization analysis of gut microbiota-immune cell interactions in malignant neoplasm of nasopharynx.\",\"authors\":\"Qicong Chen, Gang Wang, Jingcheng Shu, Xiaosu Zou, Weiwei Miao, Wenqian Nong, Min Li, Guiping Lan, Wenlin Huang, Xueying Huang, Honglin Luo, Shenhong Qu\",\"doi\":\"10.1186/s13568-025-01909-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Observational studies have suggested associations among the gut microbiome, immune cells, and the risk of malignant neoplasms of nasopharynx. 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Interestingly, the causal association of genus Candidatus Soleaferrea id.11350 was no longer significant after adjusting for two established immune cell traits (HLA DR + + monocyte %leukocyte and HLA DR + + monocyte % monocyte). Moreover, HLA DR + + monocyte %leukocyte exhibited a mediating effect (OR 0.75, 95% CI 0.59-0.96) on the causal pathway of genus Candidatus Soleaferrea id.11350-malignant neoplasms of nasopharynx, with a mediating proportion of 21.59%. To our knowledge, this study is the first to identify potential therapeutic targets and elucidate mechanistic insights for malignant neoplasms of nasopharynx interventions involving gut microbiota and immune cell traits; however, these findings warrant further validation through adequately powered randomized clinical trials (RCTs).</p>\",\"PeriodicalId\":7537,\"journal\":{\"name\":\"AMB Express\",\"volume\":\"15 1\",\"pages\":\"106\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-07-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12263519/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"AMB Express\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1186/s13568-025-01909-2\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"AMB Express","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1186/s13568-025-01909-2","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
观察性研究表明,肠道微生物群、免疫细胞和鼻咽恶性肿瘤的风险之间存在关联。然而,这些关系的因果关系尚不清楚。因此,我们进行了多次孟德尔随机化分析,以估计肠道微生物群与鼻咽部恶性肿瘤风险的因果关系,并评估免疫细胞在这一因果途径中的介导作用。从人类肠道微生物群组成(n = 211)、免疫细胞特征(n = 731)和鼻咽部恶性肿瘤的全基因组关联研究中提取的遗传变异作为计算因果关系和中介效应的工具变量。4种肠道菌群组成和8种免疫细胞特征表现出有害的因果关系,而3种肠道菌群组成和15种免疫细胞特征表现出保护作用。有趣的是,候选念珠菌属的因果关系。在调整两种已建立的免疫细胞特征(HLA DR + +单核细胞%白细胞和HLA DR + +单核细胞%单核细胞)后,11350不再显著。此外,HLA DR + +单核细胞%白细胞在候选葡萄属的致病途径中表现出中介作用(OR 0.75, 95% CI 0.59-0.96)。鼻咽部恶性肿瘤11350例,中间比例为21.59%。据我们所知,这项研究首次确定了潜在的治疗靶点,并阐明了涉及肠道微生物群和免疫细胞特征的鼻咽部恶性肿瘤干预的机制;然而,这些发现需要通过足够有力的随机临床试验(rct)进一步验证。
Mendelian randomization analysis of gut microbiota-immune cell interactions in malignant neoplasm of nasopharynx.
Observational studies have suggested associations among the gut microbiome, immune cells, and the risk of malignant neoplasms of nasopharynx. However, the causality of these relationships remains unclear. Thus, we conducted multiple Mendelian Randomization analyses to estimate the causal association of gut microbiota with the risk of malignant neoplasms of nasopharynx and to evaluate the mediating effect of immune cells on this causal pathway. Genetic variants extracted from genome-wide association studies of human gut microbiota compositions (n = 211), immune cell traits (n = 731) and malignant neoplasms of nasopharynx served as instrumental variables for calculating causal associations and mediating effects. Four gut microbiota compositions and eight immune cell traits exhibited detrimental causal effects, while three gut microbiota compositions and fifteen immune cell traits demonstrated protective effects. Interestingly, the causal association of genus Candidatus Soleaferrea id.11350 was no longer significant after adjusting for two established immune cell traits (HLA DR + + monocyte %leukocyte and HLA DR + + monocyte % monocyte). Moreover, HLA DR + + monocyte %leukocyte exhibited a mediating effect (OR 0.75, 95% CI 0.59-0.96) on the causal pathway of genus Candidatus Soleaferrea id.11350-malignant neoplasms of nasopharynx, with a mediating proportion of 21.59%. To our knowledge, this study is the first to identify potential therapeutic targets and elucidate mechanistic insights for malignant neoplasms of nasopharynx interventions involving gut microbiota and immune cell traits; however, these findings warrant further validation through adequately powered randomized clinical trials (RCTs).
期刊介绍:
AMB Express is a high quality journal that brings together research in the area of Applied and Industrial Microbiology with a particular interest in ''White Biotechnology'' and ''Red Biotechnology''. The emphasis is on processes employing microorganisms, eukaryotic cell cultures or enzymes for the biosynthesis, transformation and degradation of compounds. This includes fine and bulk chemicals, polymeric compounds and enzymes or other proteins. Downstream processes are also considered. Integrated processes combining biochemical and chemical processes are also published.