Comprehensive analysis of a 14 immune-related gene pair signature to predict the prognosis and immune features of gastric cancer

被引：13

作者：

Liu, Chuan ^{[1
]}

Chen, Bo ^{[2
]}

Huang, Zhangheng ^{[3
]}

Hu, Chuan ^{[4
]}

Jiang, Liqing ^{[1
]}

Zhao, Chengliang ^{[3
]}

机构：

[1] China Med Univ, Hosp 1, Dept Med Oncol, Shenyang 110001, Peoples R China

[2] Wenzhou Med Univ, Clin Coll 1, Wenzhou 325035, Peoples R China

[3] Chengde Med Univ, Affiliated Hosp, Dept Orthopaed Surg, Chengde 067000, Peoples R China

[4] Qingdao Univ, Affiliated Hosp, Dept Joint Surg, Qingdao 266071, Peoples R China

来源：

INTERNATIONAL IMMUNOPHARMACOLOGY | 2020年 / 89卷

关键词：

Immune-related gene pairs; Gastric cancer; Immune cells; Prognosis; Nomogram; TUMOR PROGRESSION; POOR-PROGNOSIS; T-CELLS; EXPRESSION; SURVIVAL; LANDSCAPE; NOMOGRAM; MICROENVIRONMENT; IDENTIFICATION; CHECKPOINTS;

D O I：

10.1016/j.intimp.2020.107074

中图分类号：

R392 [医学免疫学]; Q939.91 [免疫学];

学科分类号：

100102 ;

摘要：

Background: As a new method for predicting tumor prognosis, the predictive effect of immune-related gene pairs (IRGPs) has been confirmed in several cancers, but there is no comprehensive analysis of the clinical significance of IRGPs in gastric cancer (GC). Method: Clinical and gene expression profile data of GC patients were obtained from the GEO database. Based on the ImmPort database, differentially expressed immune-related gene (DEIRG) events were determined by a comparison of GC samples and adjacent normal samples. Cox proportional regression was used to construct an IRGP signature, and its availability was validated using three external validation datasets. In addition, we explored the association between clinical data and immune features and established a nomogram to predict outcomes in GC patients. Result: A total of 88 DEIRGs were identified in GC from the training set, which formed 3828 IRGPs. Fourteen overall survival (OS)-related IRGPs were used to construct the prognostic signature. As a result, patients in the high-risk group exhibited poorer OS compared to those in the low-risk group. In addition, the fraction of CD8+ T cells, plasma cells, CD4 memory activated T cells, and M1 macrophages was higher in the high-risk group. Expression of two immune checkpoints, CD276 and VTCN1, was significantly higher in the high-risk group as well. Based on the independent prognostic factors, a nomogram was established and showed excellent performance. Conclusion: The 14 OS-related IRGP signature was associated with OS, immune cells, and immune checkpoints in GC patients, and it could provide the basis for related immunotherapy.

引用

页数：9