肠道微生物群和新陈代谢动态沿着胃癌的进展:一个探索性的多omics分析
Jingfang Yang1, Binbin Wang1, Yanfei Yu1
1Gastroenterology Department, The People's Hospital of Chizhou, 247100 Chizhou, Anhui, China.
Frontiers in bioscience (Landmark edition)
|January 29, 2026
概括
胃癌的进展涉及显著的肠道微生物群和代谢变化. 缩是一个关键的拐点,结合微生物和代谢物签名,为早期检测提供了潜在的潜力.
科学领域:
- 微生物学 微生物学
- 代谢学 代谢学 代谢学
- 胃肠病学 胃肠病学
背景情况:
- 胃癌 (GC) 是一个主要的全球健康问题,其原因复杂.
- 科雷亚序列描述了从胃炎到癌的GC发展.
- 肠道微生物群失调和代谢变化与GC有关,但它们的综合作用尚不清楚.
研究的目的:
- 调查整个科雷亚序列的综合肠道微生物群和代谢动态.
- 为了确定胃癌进展中的特定阶段的微生物和代谢变化.
- 探索这些变化的诊断潜力.
主要方法:
- 在五个阶段招募了参与者:正常,胃炎,缩,侵蚀和GC.
- 分析了便和胃样本,使用16S rRNA测序和非目标代谢学.
- 通过ROC曲线评估微生物多样性,确定差异化代谢物,并评估诊断潜力.
主要成果:
- 随着GC的进展,微生物多样性下降,并观察到特定的细菌转移.
- 缩标志着一种代谢断点,减少了抗炎性SCFA和增加了促炎性代谢物.
- 动因细菌对GC检测表现出强大的区分能力 (AUC为0.935).
结论:
- 综合分析揭示了在Correaa序列上的特定阶段的微生物和代谢变化.
- 缩是一个关键的拐点,侵蚀是GC发展中的过渡状态.
- 结合的微生物群-代谢物签名显示出非侵入性GC检测和分层的前景.
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