Evidence map›Paper›PMID 36072968›Full record

ArticleJournal of oncology2022

Gut Microbiota Dysbiosis in the Development and Progression of Gastric Cancer.

Yingying Miao, Hui Tang, Qizhi Zhai, Lu Liu, Lu Xia, Wenhan Wu, Yue Xu, Jianning Wang

Open access · hybridAbstract read
In one paragraph

Article in Journal of oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 18 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Yingying MiaoDepartment of Gastroenterology, The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing 211199, China.ORCID https://orcid.org/0000-0002-2764-3319
Hui TangShanghai Biotecan Pharmaceuticals Co., Ltd., Shanghai 201204, China.ORCID https://orcid.org/0000-0002-7429-1627
Qizhi ZhaiDepartment of Gastroenterology, The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing 211199, China.ORCID https://orcid.org/0000-0003-0121-0942
Lu LiuDepartment of Gastroenterology, The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing 211199, China.ORCID https://orcid.org/0000-0002-7715-6690
Lu XiaDepartment of Gastroenterology, The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing 211199, China.ORCID https://orcid.org/0000-0002-3475-4172
Wenhan WuShanghai Biotecan Pharmaceuticals Co., Ltd., Shanghai 201204, China.ORCID https://orcid.org/0000-0003-1906-834X
Yue XuShanghai Biotecan Pharmaceuticals Co., Ltd., Shanghai 201204, China.ORCID https://orcid.org/0000-0002-5461-5495
Jianning WangDepartment of Gastroenterology, The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing 211199, China.ORCID https://orcid.org/0000-0001-5911-7834
Nanjing Jiangning Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: This study aims to explore gut microbiota dysbiosis in the histological stages of gastric cancer (GC). Methods: Feces samples and clinical characteristics were collected from patients with different stages of GC, including 15 superficial gastritis (SG), 13 atrophic gastritis (AG), 8 gastric mucosal atypical hyperplasia (GMAH), and 15 advanced GC cases. The diversity and composition of gut microbiota among the four groups were determined by sequencing the V4 region of bacterial 16S rRNA genes. Results: Reduced gut microbial alpha diversity and altered dissimilarity of the microbial community structure were found among the four groups. In addition, 18 species, 6 species, 6 species, and 16 species of bacteria were enriched in the SG, AG, GMAH, and GC groups, respectively, using the linear discriminant analysis (LDA) effect size (LEfSe) analyses. Besides, we found that two new genera, Conclusions: We identified differences in microbial compositional changes across stages of GC. Six genera and two metabolic pathways were more abundant in the GC group than noncancer groups, suggesting that these findings may contribute to the therapy strategies in GC in the near feature.

Identifiers

PMID36072968
PMCPMC9441395
OpenAlexW4293660516

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.