Evidence map›Paper›PMID 32908454›Full record

ArticleCancer cell international2020

Establishment of a 5-gene risk model related to regulatory T cells for predicting gastric cancer prognosis.

Gang Hu, Ningjie Sun, Jiansong Jiang, Xiansheng Chen

Abstract read
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Article in Cancer cell international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

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10citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Gang HuDepartment of Gastrointestinal Surgery, Yiwu Central Hospital, 699# Jiangdong Road, Jiangdong Street, 322000 Jinhua, China.ORCID 0000-0002-6615-3371
Ningjie SunDepartment of Gastrointestinal Surgery, Yiwu Central Hospital, 699# Jiangdong Road, Jiangdong Street, 322000 Jinhua, China.
Jiansong JiangDepartment of Gastrointestinal Surgery, Yiwu Central Hospital, 699# Jiangdong Road, Jiangdong Street, 322000 Jinhua, China.
Xiansheng ChenDepartment of Gastrointestinal Surgery, Yiwu Central Hospital, 699# Jiangdong Road, Jiangdong Street, 322000 Jinhua, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastric cancer (GC) is one of the high-risk cancers that lacks effective methods for prognosis prediction. Therefore, we searched for immune cells related to the prognosis of GC and studied the role of related genes in GC prognosis.

methodsIn this study, we collected the mRNA data of GC from The Cancer Genome Atlas (TCGA) database and studied the immune cells that were closely related to the prognosis of GC. Spearman correlation analysis was performed to show the association between immune cell-related genes and the differentially expressed genes (DEGs) of GC. Univariate and multivariate Cox regression analyses were conducted on the immune cell-related genes with a high correlation with GC. A prognostic risk score model was constructed and the most significant feature genes were identified. Kaplan-Meier method was then used to compare the overall survival (OS) of patients with high-risk and low-risk, and receiver operating characteristic (ROC) analysis was used to assess the accuracy of the risk model. In addition, GC patients were grouped according to the median expression of the features genes, and survival analysis was further carried out.

resultsIt was noted that regulatory T cells (Tregs) were significantly correlated with the prognosis of GC, and 172 genes related to Tregs were found to be closely associated with GC. An optimal prognostic risk model was constructed, and a 5-gene (including LRFN4, ADAMTS12, MCEMP1, HP and MUC15) signature-based risk score was established. Survival analysis showed significant difference in OS between low-risk and high-risk samples. ROC analysis results indicated that the risk model had a high accuracy for the prognosis prediction of samples (AUC = 0.717). The results of survival analysis on each feature gene based on expression levels were consistent with the results of multivariate Cox analysis for predicting the risk rate of the 5 genes.

conclusionThese results proved that the 5-gene signature-based risk score could be used to predict the survival of GC patients, and these 5 genes were closely related to Tregs. These findings are of great significance for studying the role of immune cells and related immune factors in regulating the prognosis of GC.

Indexed as

Gastric cancermRNA signaturePrognosis predictionRegulatory T cellsTCGA

Identifiers

PMID32908454
PMCPMC7470613

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