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不同亚型胃癌和胃肠道间质瘤患者的肠道微生物群

Gut microbiota of patients with different subtypes of gastric cancer and gastrointestinal stromal tumors.

作者信息

Sarhadi Virinder, Mathew Binu, Kokkola Arto, Karla Tiina, Tikkanen Milja, Rautelin Hilpi, Lahti Leo, Puolakkainen Pauli, Knuutila Sakari

机构信息

Faculty of Medicine, Department of Pathology, University of Helsinki, 00014, Helsinki, Finland.

Department of Computing, University of Turku, Turku, Finland.

出版信息

Gut Pathog. 2021 Feb 17;13(1):11. doi: 10.1186/s13099-021-00403-x.

Abstract

BACKGROUND

Gastric adenocarcinoma is associated with H. pylori infection and inflammation that can result in the dysbiosis of gastric microbiota. The association of intestinal microbiota with gastric adenocarcinoma subtypes or with gastric gastrointestinal stromal tumors (GIST) is however not well known. Therefore, we performed 16S rRNA gene sequencing on DNA isolated from stool samples of Finnish patients and controls to study differences in microbiota among different histological subtypes of gastric adenocarcinoma, gastric GIST and healthy controls.

RESULTS

We found that gut microbiota alpha diversity was lowest in diffuse adenocarcinoma patients, followed by intestinal type and GIST patients, although the differences were not significant compared to controls. Beta-diversity analysis however showed significant differences in microbiota composition for all subtypes compared to controls. Significantly higher abundance of Enterobacteriaceae was observed in both adenocarcinoma subtypes, whereas lower abundance of Bifidobacteriaceae was seen only in diffuse adenocarcinoma and of Oscillibacter in intestinal adenocarcinoma. Both GIST and adenocarcinoma patients had higher abundance of Enterobacteriaceae and lower abundance of Lactobacillaceae and Oscillibacter while lower abundance of Lachnoclostridium, Bifidobacterium, Parabacteroides and Barnesiella was seen only in the adenocarcinoma patients.

CONCLUSIONS

Our analysis shows association of higher Enterobacteriaceae abundance with all types of gastric tumors. Therefore it could be potentially useful as a marker of gastric malignancies. Lower gut microbiota diversity might be indicative of poorly differentiated, invasive, advanced or aggressive tumors and could possibly be a prognostic marker for gastric tumors.

摘要

背景

胃腺癌与幽门螺杆菌感染及炎症相关,后者可导致胃微生物群失调。然而,肠道微生物群与胃腺癌亚型或胃肠道间质瘤(GIST)之间的关联尚不清楚。因此,我们对芬兰患者和对照组粪便样本中分离的DNA进行了16S rRNA基因测序,以研究胃腺癌不同组织学亚型、胃GIST和健康对照组之间微生物群的差异。

结果

我们发现,弥漫性腺癌患者的肠道微生物群α多样性最低,其次是肠型和GIST患者,尽管与对照组相比差异不显著。然而,β多样性分析显示,所有亚型的微生物群组成与对照组相比均存在显著差异。在两种腺癌亚型中均观察到肠杆菌科的丰度显著更高,而双歧杆菌科的丰度仅在弥漫性腺癌中较低,颤杆菌属在肠腺癌中较低。GIST和腺癌患者的肠杆菌科丰度均较高,而乳酸杆菌科和颤杆菌属的丰度较低,而仅在腺癌患者中观察到瘤胃球菌属、双歧杆菌属、副拟杆菌属和巴恩斯氏菌属的丰度较低。

结论

我们的分析表明,肠杆菌科丰度升高与所有类型的胃肿瘤相关。因此,它可能作为胃恶性肿瘤的标志物。较低的肠道微生物群多样性可能表明肿瘤分化差、具有侵袭性、处于晚期或具有侵袭性,并且可能是胃肿瘤的预后标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1568/7888145/4551fd2ca6ed/13099_2021_403_Fig1_HTML.jpg

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