Kadeerhan Gaohaer, Gerhard Markus, Gao Juan-Juan, Mejías-Luque Raquel, Zhang Lian, Vieth Michael, Ma Jun-Ling, Bajbouj Monther, Suchanek Stepan, Liu Wei-Dong, Ulm Kurt, Quante Michael, Li Zhe-Xuan, Zhou Tong, Schmid Roland, Classen Meinhard, Li Wen-Qing, Zhang Yang, You Wei-Cheng, Pan Kai-Feng
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Cancer Epidemiology, Peking University Cancer Hospital & Institute Beijing, China.
PYLOTUM Key Joint Laboratory for Upper GI Cancer, Technische Universität München, Munich, Germany, Peking University Cancer Hospital & Institute Beijing, China.
Am J Cancer Res. 2021 Feb 1;11(2):561-575. eCollection 2021.
In addition to Helicobacter pylori (H.pylori), gastric microbiota may be involved in carcinogenesis process. However, the longitudinal study to assess changes in the gastric microbiota associated with the development of gastric carcinogenesis is still limited. The aim of this study is to explore dynamic microbial alterations in gastric cancer (GC) development based on a 4-year endoscopic follow-up cohort in Linqu County, China. Microbial alterations were investigated by deep sequencing of the microbial 16S ribosomal RNA gene in 179 subjects with various gastric lesions, and validated in paired gastric biopsies prospectively collected before and after lesion progression and in non-progression controls. Significant differences were found in microbial diversity and community structure across various gastric lesions, with 62 candidate differential taxa between at least two lesion groups. Further validations identified Helicobacter, Bacillus, Capnocytophaga and Prevotella to be associated with lesion progression-to-dysplasia (DYS)/GC (all P < 0.05), especially for subjects progressing from intestinal metaplasia (IM) to DYS/GC. The combination of the four genera in a microbial dysbiosis index showed a significant difference after lesion progression-to-DYS/GC compared to controls (P = 0.027). The panel including the four genera identified subjects after progression-to-DYS/GC with an area under the receiver-operating curve (AUC) of 0.941. Predictive significance was found before lesion progression-to-DYS/GC with an AUC = 0.776 and an even better AUC (0.927) for subjects progressing from IM to DYS/GC. Microbiota may play different roles at different stages in gastric carcinogenesis. A panel of bacterial genera associated with gastric lesions may help to assess gastric microbial dysbiosis and show potential predictive values for lesion progression. Our findings provide new clues for the microbial mechanism of H.pylori-associated carcinogenesis.
除幽门螺杆菌(H.pylori)外,胃微生物群可能参与致癌过程。然而,评估与胃癌发生发展相关的胃微生物群变化的纵向研究仍然有限。本研究的目的是基于中国临朐县一个为期4年的内镜随访队列,探索胃癌(GC)发生发展过程中的动态微生物变化。通过对179例患有各种胃部病变的受试者的微生物16S核糖体RNA基因进行深度测序来研究微生物变化,并在病变进展前后前瞻性收集的配对胃活检组织以及未进展的对照中进行验证。在各种胃部病变中发现微生物多样性和群落结构存在显著差异,至少两个病变组之间有62个候选差异分类群。进一步验证发现,幽门螺杆菌属、芽孢杆菌属、二氧化碳嗜纤维菌属和普雷沃菌属与病变进展为发育异常(DYS)/胃癌相关(所有P<0.05),特别是对于从肠化生(IM)进展为DYS/GC的受试者。这四个属在微生物失调指数中的组合在病变进展为DYS/GC后与对照组相比有显著差异(P = 0.027)。包括这四个属的组合在病变进展为DYS/GC后识别受试者的受试者工作特征曲线下面积(AUC)为0.941。在病变进展为DYS/GC之前发现有预测意义,AUC = 0.776,对于从IM进展为DYS/GC的受试者,AUC甚至更高(0.927)。微生物群在胃癌发生的不同阶段可能发挥不同作用。一组与胃部病变相关的细菌属可能有助于评估胃微生物失调,并对病变进展显示出潜在的预测价值。我们的发现为幽门螺杆菌相关致癌作用的微生物机制提供了新线索。