Evidence map›Paper›PMID 36388039›Full record

ArticleTranslational cancer research2022

Novel insight on predicting prognosis of gastric cancer based on inflammation.

Zhizhan Ni, Jiuqiang Zhang, Chenshen Huang, Huahao Xie, Bujun Ge, Qi Huang

Abstract read
In one paragraph

Article in Translational cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

6 authors.

Zhizhan Ni *Department of General Surgery, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Jiuqiang Zhang *Department of General Surgery, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Chenshen Huang *Department of General Surgery, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Huahao XieDepartment of General Surgery, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Bujun GeDepartment of General Surgery, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Qi HuangDepartment of General Surgery, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The tumor microenvironment (TME) and inflammation play vital roles in the development and progression of gastric cancer (GC). However, there are no inflammation-related models that can predict the prognosis and immunotherapy response of GC patients. We aimed to establish a prognostic model based on an inflammation-related gene (IRG) signature that can predict poor clinical outcomes in GC. Methods: We searched IRGs in The Cancer Genome Atlas (TCGA) database and identified genes differentially expressed in GC. The model was constructed using univariate Cox and least absolute shrinkage and selection operator (LASSO) regression analysis and validated using Gene Expression Omnibus (GEO) database. Receiver operating characteristic (ROC) curve, principal component analysis (PCA), and t-distribution stochastic neighbor embedding (t-SNE) analysis were performed to evaluate model performance. Independent prognostic factor, immune infiltration, cancer stemness, immunotherapy response analysis and gene set enrichment analysis (GSEA) were performed for functional evaluation. Results: An inflammation-related risk model was established based on 8 genes ( Conclusions: We established and validated an inflammation-related prognostic model that predicts immune escape and patient prognosis in GC. Our model is expected to improve clinical outcomes by facilitating clinical decision making and the development of individualized treatments.

Indexed as

Gastric cancer (GC)immune infiltrationimmunotherapyinflammationprognosis

Identifiers

PMID36388039
PMCPMC9641120

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