子宫内膜癌中多态微生物群的导航复杂性。

IF 9.2 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Nicole R Jimenez, Chloe R Herman, Paweł Łaniewski, Emily Cope, Keehoon Lee, Nichole D Mahnert, Dana M Chase, J Gregory Caporaso, Melissa M Herbst-Kralovetz
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引用次数: 0

摘要

微生物组是了解子宫内膜癌(EC)病因和预防策略的关键,涉及雌激素驱动型癌症中雌激素的调节。利用QIIME 2平台的强大方法,我们检查了来自EC队列的16S rRNA阴道和直肠微生物组数据:192名患有良性妇科疾病、子宫内膜增生或子宫内膜癌的女性。鉴定出EC特有的不同微生物组成和群落网络,并将其与EC危险因素调整后的组织学分级相关。阴道健康相关的乳酸杆菌和乳酸杆菌,直肠普雷沃氏菌和嗜胃杆菌在EC中减少,而有害的阴道厌氧球菌、卟啉单胞菌、普雷沃氏菌、嗜胃杆菌和直肠布蒂axella则增加。EC直肠和阴道部位的显著细菌特征是相同的,如普雷沃氏菌(Prevotella timonensis)和嗜胃杆菌(Peptoniphilus A.)。阴道乳酸杆菌的丰富导致直肠特征共享较少。假定的微生物代谢分析确定了EC患者中氨基酸、复合碳水化合物和激素代谢的失调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Navigating complexities of polymorphic microbiomes in endometrial cancer.

The microbiome is key to understanding endometrial cancer (EC) etiology and prevention strategies, implicated in the regulation of estrogen in estrogen-driven cancers. Utilizing robust methodologies in the QIIME 2 platform, we examined 16S rRNA vaginal and rectal microbiome data from an EC cohort: 192 women with benign gynecologic conditions, endometrial hyperplasia, or endometrial cancer. Distinct microbial compositions and community networks specific to EC were identified and related to histological grade with adjustments for EC risk factors. Vaginal health-associated Lactobacillus and Limosilactobacillus, and rectal Prevotella and Peptoniphilus, were depleted in EC, while detrimental vaginal Anaerococcus, Porphyromonas, Prevotella, Peptoniphilus, and rectal Buttiaxella were enriched. Significant bacterial features were shared between rectal and vaginal sites in EC, such as Prevotella timonensis and Peptoniphilus A. Vaginal Lactobacillus abundance contributed to less feature sharing from the rectum. Putative microbial metabolic analysis identified dysregulation of amino acid, complex carbohydrate, and hormone metabolism amongst patients with EC.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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