Orchestrating the gut microbiota-mitochondrial-immune axis in gynecological diseases: mechanisms and dual-targeting therapeutic strategies.

IF 3.1 Q2 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Frontiers in reproductive health Pub Date : 2026-07-01 eCollection Date: 2026-01-01 DOI:10.3389/frph.2026.1845581
Haixia Tang, Yiting Zhang, Yanting Wang, Ze Zhou, Rong Sun, Rong Chen, Lijuan Yang, Mengqiu Shao, Jiabao Liao
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引用次数: 0

Abstract

The "gut microbiota-mitochondria axis" has become the core hub connecting the metabolism, immunity, and endocrine regulation of gynecological diseases. In this review, the hierarchical regulation mechanism of this axis is systematically combed: at the upstream level, intestinal short-chain fatty acids (SCFAs), bile acids (BAs), tryptophan derivatives, and other metabolites can activate AMPK/PGC-1α, FXR/TGR5, and AhR-mediated energy sensing and receptor signaling pathways; On the functional level, bacterial lipopolysaccharide-TLR4 signal and cGAS-STING/NLRP3 inflammasome pathway activated by cytoplasmic mitochondrial DNA (mtDNA) can amplify innate immune response; At the effect level, mitochondrial reactive oxygen species (ROS), mitochondrial dynamics, and PINK1/Parkin-mediated mitophagy are the common key nodes to regulate mitochondrial quality and inflammatory response. Combined with the two-way relationship between the estrobolome and steroid production, the above processes together form a self-reinforcing closed loop of "metabolic input-immune amplification-oxidative stress/autophagy-endocrine regulation". Based on this theoretical framework, this paper analyzes the disease-specific correlations among polycystic ovary syndrome, endometriosis, premature ovarian insufficiency, and gynecological malignancies, and puts forward a dual-targeted treatment idea with research value. The intervention plan with microbiota as the core aims to adjust the metabolite spectrum and endotoxin level; Mitochondria-centered interventions focus on restoring cell energy metabolism and apoptosis sensitivity. In addition, this review constructs a hierarchical research framework of "microbiota-metabolomics-mitochondria" to clarify the targeted phenotypes in the pathway, and provide guidance for subsequent clinical trial design and long-term monitoring. With the deep integration of multi-omics technology and targeted interventions, the gut microbiota-mitochondria axis is expected to become an important breakthrough in precision medical treatment of gynecological diseases and build a brand-new bridge between basic mechanism research and clinical transformation.

协调肠道微生物-线粒体-免疫轴在妇科疾病:机制和双靶向治疗策略。
“肠道微生物-线粒体轴”已成为连接妇科疾病代谢、免疫、内分泌调节的核心枢纽。本文系统梳理了该轴的分级调控机制:在上游水平,肠道短链脂肪酸(SCFAs)、胆汁酸(BAs)、色氨酸衍生物等代谢产物可激活AMPK/PGC-1α、FXR/TGR5、ahr介导的能量传感和受体信号通路;在功能水平上,胞质线粒体DNA (mtDNA)激活的细菌脂多糖- tlr4信号和cGAS-STING/NLRP3炎性小体通路可放大先天免疫应答;在效应水平上,线粒体活性氧(ROS)、线粒体动力学和PINK1/ parkinson介导的线粒体自噬是调节线粒体质量和炎症反应的共同关键节点。结合雌激素与类固醇产生的双向关系,上述过程共同形成了“代谢输入-免疫放大-氧化应激/自噬-内分泌调节”的自我强化闭环。基于这一理论框架,分析多囊卵巢综合征、子宫内膜异位症、卵巢早衰与妇科恶性肿瘤的疾病特异性相关性,提出具有研究价值的双靶向治疗思路。以菌群为核心的干预方案旨在调节代谢物谱和内毒素水平;以线粒体为中心的干预侧重于恢复细胞能量代谢和凋亡敏感性。此外,本文构建了“微生物-代谢组学-线粒体”的分层研究框架,以明确该通路中的靶向表型,为后续临床试验设计和长期监测提供指导。随着多组学技术与靶向干预的深度融合,肠道微生物-线粒体轴有望成为妇科疾病精准医疗的重要突破,在基础机制研究与临床转化之间架起崭新的桥梁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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