Department of Gastroenterology and Hepatology, The First Medical Center, Chinese PLA General Hospital, Medical School of Chinese PLA, Beijing, China.
Department of Gastroenterology, Civil Aviation General Hospital, Beijing, China.
Front Cell Infect Microbiol. 2021 Mar 10;11:640309. doi: 10.3389/fcimb.2021.640309. eCollection 2021.
To characterize the salivary microbiota in patients at different progressive histological stages of gastric carcinogenesis and identify microbial markers for detecting gastric cancer, two hundred and ninety-three patients were grouped into superficial gastritis (SG; n = 101), atrophic gastritis (AG; n = 93), and gastric cancer (GC; n = 99) according to their histology. 16S rRNA gene sequencing was used to access the salivary microbiota profile. A random forest model was constructed to classify gastric histological types based on the salivary microbiota compositions. A distinct salivary microbiota was observed in patients with GC when comparing with SG and AG, which was featured by an enrichment of putative proinflammatory taxa including and . Among the significantly decreased oral bacteria in GC patients including , , , , , and , , and are known to reduce nitrite, which may consequently result in an accumulation of carcinogenic N-nitroso compounds. We found that GC can be distinguished accurately from patients with AG and SG (AUC = 0.91) by the random forest model based on the salivary microbiota profiles, and taxa belonging to and have potential as diagnostic biomarkers for GC. Remarkable changes in the salivary microbiota functions were also detected across three histological types, and the upregulation in the isoleucine and valine is in line with a higher level of these amino acids in the gastric tumor tissues that reported by other independent studies. Conclusively, bacteria in the oral cavity may contribute gastric cancer and become new diagnostic biomarkers for GC, but further evaluation against independent clinical cohorts is required. The potential mechanisms of salivary microbiota in participating the pathogenesis of GC may include an accumulation of proinflammatory bacteria and a decline in those reducing carcinogenic N-nitroso compounds.
为了描述处于不同胃肿瘤发生进展阶段的患者的唾液微生物群,并鉴定用于检测胃癌的微生物标志物,根据组织学将 293 名患者分为浅表性胃炎(SG;n = 101)、萎缩性胃炎(AG;n = 93)和胃癌(GC;n = 99)。使用 16S rRNA 基因测序来评估唾液微生物群的组成。基于唾液微生物群组成,构建随机森林模型来分类胃组织学类型。与 SG 和 AG 相比,GC 患者的唾液微生物群明显不同,其特征是假定促炎分类群的丰度增加,包括 和 。在 GC 患者中显著减少的口腔细菌包括 、 、 、 、 和 ,已知这些细菌减少亚硝酸盐,这可能导致致癌性 N-亚硝基化合物的积累。我们发现,基于唾液微生物群组成的随机森林模型可以准确地区分 GC 患者与 AG 和 SG 患者(AUC = 0.91),属于 和 的分类群具有作为 GC 诊断生物标志物的潜力。在三个组织学类型中也检测到唾液微生物群功能的显著变化,亮氨酸和缬氨酸的上调与其他独立研究报道的胃肿瘤组织中这些氨基酸水平升高一致。总之,口腔细菌可能有助于胃癌的发生,并成为 GC 的新诊断生物标志物,但需要对独立的临床队列进行进一步评估。唾液微生物群参与 GC 发病机制的潜在机制可能包括促炎细菌的积累和减少致癌 N-亚硝基化合物的细菌减少。