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胃肿瘤发生中的黏膜微生物组失调。

Mucosal microbiome dysbiosis in gastric carcinogenesis.

机构信息

Department of Medicine and Therapeutics, Institute of Digestive Disease, State Key Laboratory of Digestive Disease, Li Ka Shing Institute of Health Sciences, CUHK Shenzhen Research Institute, The Chinese University of Hong Kong, Hong Kong, China.

State Key Laboratory of Cancer Biology, Xijing Hospital, Fourth Military Medical University, Xian, China.

出版信息

Gut. 2018 Jun;67(6):1024-1032. doi: 10.1136/gutjnl-2017-314281. Epub 2017 Aug 1.

Abstract

OBJECTIVES

We aimed to characterise the microbial changes associated with histological stages of gastric tumourigenesis.

DESIGN

We performed 16S rRNA gene analysis of gastric mucosal samples from 81 cases including superficial gastritis (SG), atrophic gastritis (AG), intestinal metaplasia (IM) and gastric cancer (GC) from Xi'an, China, to determine mucosal microbiome dysbiosis across stages of GC. We validated the results in mucosal samples of 126 cases from Inner Mongolia, China.

RESULTS

We observed significant mucosa microbial dysbiosis in IM and GC subjects, with significant enrichment of 21 and depletion of 10 bacterial taxa in GC compared with SG (q<0.05). Microbial network analysis showed increasing correlation strengths among them with disease progression (p<0.001). Five GC-enriched bacterial taxa whose species identifications correspond to , , , and had significant centralities in the GC ecological network (p<0.05) and classified GC from SG with an area under the receiver-operating curve (AUC) of 0.82. Moreover, stronger interactions among gastric microbes were observed in -negative samples compared with -positive samples in SG and IM. The fold changes of selected bacteria, and strengths of their interactions were successfully validated in the Inner Mongolian cohort, in which the five bacterial markers distinguished GC from SG with an AUC of 0.81.

CONCLUSIONS

In addition to microbial compositional changes, we identified differences in bacterial interactions across stages of gastric carcinogenesis. The significant enrichments and network centralities suggest potentially important roles of , , , and in GC progression.

摘要

目的

我们旨在描述与胃肿瘤发生的组织学阶段相关的微生物变化。

设计

我们对来自中国西安的 81 例胃黏膜样本进行了 16S rRNA 基因分析,包括浅表性胃炎(SG)、萎缩性胃炎(AG)、肠上皮化生(IM)和胃癌(GC),以确定 GC 各阶段胃黏膜微生物群落失调。我们在中国内蒙古的 126 例黏膜样本中验证了这些结果。

结果

我们观察到 IM 和 GC 受试者的黏膜微生物明显失调,与 SG 相比,GC 受试者中 21 种细菌丰富,10 种细菌减少(q<0.05)。微生物网络分析显示,随着疾病的进展,它们之间的相关性强度增加(p<0.001)。在 GC 生态网络中,5 种 GC 富集的细菌分类群的物种鉴定分别对应于、、、和 ,具有显著的中心性(p<0.05),并将 GC 与 SG 区分开来,ROC 曲线下面积(AUC)为 0.82。此外,在 SG 和 IM 中,与 -阳性样本相比,-阴性样本中胃微生物之间的相互作用更强。在内蒙古队列中成功验证了所选细菌的倍数变化及其相互作用的强度,其中 5 种细菌标志物将 GC 与 SG 区分开来,AUC 为 0.81。

结论

除了微生物组成变化外,我们还发现了胃癌变各阶段细菌相互作用的差异。显著的富集和网络中心性表明 、、、和 可能在 GC 进展中具有重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcbf/5969346/988dfd98fb38/gutjnl-2017-314281f01.jpg

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