Evidence map›Paper›PMID 31609743›Full record

ArticleClinical and translational gastroenterology2019

Gut Microbiota Functional Biomolecules With Immune-Lipid Metabolism for a Prognostic Compound Score in Epstein-Barr Virus-Associated Gastric Adenocarcinoma: A Pilot Study.

Fang Wang, Jingyi Wu, Yan Wang, Yufen Jin, Xin Jiang, Zhichao Qiu, Yan Qin, Yankui Liu, Xiaowei Qi, Xiaosong Ge and 3 more

Abstract read
In one paragraph

Article in Clinical and translational gastroenterology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. How Does Epstein-Barr Virus Interact With Other Microbiomes in EBV-Driven Cancers?Frontiers in cellular and infection microbiology · 2022
    Review
  3. Review
  4. Tumor-Associated Microbiome: Where Do We Stand?International journal of molecular sciences · 2021
    Review
  5. Article
  6. Article
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

13 authors.

Fang WangDepartment of Oncology, Affiliated Hospital of Jiangnan University, Wuxi, China.
Jingyi WuDepartment of Oncology, Affiliated Hospital of Jiangnan University, Wuxi, China.
Yan WangDepartment of Oncology, Affiliated Hospital of Jiangnan University, Wuxi, China.
Yufen JinDepartment of Oncology, Affiliated Hospital of Jiangnan University, Wuxi, China.
Xin JiangDepartment of Oncology, Affiliated Hospital of Jiangnan University, Wuxi, China.
Zhichao QiuDepartment of Oncology, Affiliated Hospital of Jiangnan University, Wuxi, China.
Yan QinDepartment of Pathology, Affiliated Hospital of Jiangnan University, Wuxi, China.
Yankui LiuDepartment of Pathology, Affiliated Hospital of Jiangnan University, Wuxi, China.
Xiaowei QiDepartment of Pathology, Affiliated Hospital of Jiangnan University, Wuxi, China.
Xiaosong GeDepartment of Oncology, Affiliated Hospital of Jiangnan University, Wuxi, China.
Yong MaoDepartment of Oncology, Affiliated Hospital of Jiangnan University, Wuxi, China.
Yang ChengDepartment of Public Health and Preventive Medicine, Wuxi School of Medicine, Jiangnan University, Wuxi, China.
Dong HuaDepartment of Oncology, Affiliated Hospital of Jiangnan University, Wuxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIncreasing evidence has indicated an association between gut microbiota in gastrointestinal cancer and clinical outcome. Herein, we aim to develop a prognosis-prediction tool based on an immune-lipid metabolism signature, tumor cell-associated immune microenvironment, and lipid metabolism proteins inferred from the function of gut microbiota.

methods16S gene ribosomal RNA sequencing was performed on 10 fecal samples obtained after tumor resection but before chemotherapy (EBVaGC = 4 and EBVnGC = 6). Least absolute shrinkage and selection operator (LASSO) Cox regression was applied to screening for highly accurate marker proteins. A compound score based on the fraction of screened markers was then constructed using a LASSO logistic regression model.

resultsThe Tax4Fun analysis based on Kyoto Encyclopedia of Genes and Genomes data indicated differentially expressed tumor pathway between EBVnGC and EBVaGC. Using the LASSO logistic model, a compound score was established consisting of 14 types of immune microenvironment and lipid metabolism proteins. In the training set (378 patients), significant differences were found between high- and low-compound score groups in overall survival across and within subpopulations with an identical EBV. Multivariable analysis revealed that the compound score was an independent prognostic factor (hazard ratio, 2.26; 95% confidence interval = 2.28-3.36). The prognostic value ;of the compound score was also confirmed in the validation (162 patients) and entire (540 patients) sets. DISCUSSION: The proposed compound score is a promising signature for estimating overall survival in patients with gastric cancer having EBVaGCs or EBVnGCs.

Indexed as

AdenocarcinomaBiomarkers, TumorChemotherapy, AdjuvantDNA, BacterialEpstein-Barr Virus InfectionsFeasibility StudiesFecesFemaleFollow-Up StudiesGastrectomyGastrointestinal MicrobiomeHerpesvirus 4, HumanHumansKaplan-Meier EstimateLipid MetabolismMaleBiomarkers, TumorDNA, BacterialRNA, Ribosomal, 16S

Identifiers

PMID31609743
PMCPMC6884346

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Registered trials

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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.