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pmid:33661721

Construction of an immune-related gene signature to predict survival and treatment outcome in gastric cancer.

Shuairan Zhang · Zhi Li · Hang Dong · Peihong Wu · Yang Liu · Tianshu Guo · Ce Li · Shuo Wang · Xiujuan Qu · Yunpeng Liu · Xiaofang Che · Ling Xu

Science progress · 2021 doi:10.1177/0036850421997286

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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title
Construction of an immune-related gene signature to predict survival and treatment outcome in gastric cancer.
doi
10.1177/0036850421997286
pmid
33661721
authors array · 12 items
[0]
Shuairan Zhang
[1]
Zhi Li
[2]
Hang Dong
[3]
Peihong Wu
[4]
Yang Liu
[5]
Tianshu Guo
[6]
Ce Li
[7]
Shuo Wang
[8]
Xiujuan Qu
[9]
Yunpeng Liu
[10]
Xiaofang Che
[11]
Ling Xu
journal
Science progress
year
2021
abstract
Immune cells have emerged as key regulators in the occurrence and development of multiple tumor types. However, it is unclear whether immune-related genes (IRGs) and the tumor immune microenvironment can predict prognosis for patients with gastric cancer (GC). The mRNA expression data in GC tissues (n = 368) were obtained from The Cancer Genome Atlas (TCGA) database. Differentially expressed IRGs in patients with GC were determined using a computational difference algorithm. A prognostic signature was constructed using COX regression and random survival forest (RSF) analyses. In addition, datasets related to "gemcitabine resistance" and "trastuzumab resistance" (GSE58118 and GSE77346) were obtained for GEO database, and DEGs associated with drug-resistance were screened. Then, we analyzed correlations between gene expression and cancer immune infiltrates via Tumor Immune Estimation Resource (TIMER) site. The cBioportal database was used to analyze drug-resistant gene mutation status and survival. One hundred and fifty-five differentially expressed IRGs were screened between GC and normal tissues, and a prognostic signature consisting of four IRGs (NRP1, PPP3R1, IL17RA, and FGF16) was closely related to the overall survival (OS). According to cutoff value of risk score, patients were divided into high-risk and low-risk group. Patients in the high-risk group had shorter OS compared to the low-risk group in both the training (p < 0.0001) and testing sets (p = 0.0021). In addition, we developed a 5-IRGs (LGR6, DKK1, TNFRSF1B, NRP1, and CXCR4) signature which may participate in drug resistance processes in GC. Survival analysis showed that patients with drug-resistant gene mutations had shorter OS (p = 0.0459) and DFS (p < 0.001). We constructed four survival-related IRGs and five IRGs related to drug resistance which may contribute to predict the prognosis of GC.
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Gene expression signature of gemcitabine resistance in human gastric cancer cell line
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The four-IRGs signature-based prognosis model improve GC survival prediction
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33661721", "kind": "science-record", "revision": 7, "content_hash": "sha256:b9a0101c779d337500d62100dcfc14c4736c1f8bdfd10b94a60c0025991dbc04", "created_at": "2026-11-01T15:41:27Z", "updated_at": "2026-11-01T21:24:46Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Construction of an immune-related gene signature to predict survival and treatment outcome in gastric cancer.", "doi": "10.1177/0036850421997286", "pmid": "33661721", "authors": ["Shuairan Zhang", "Zhi Li", "Hang Dong", "Peihong Wu", "Yang Liu", "Tianshu Guo", "Ce Li", "Shuo Wang", "Xiujuan Qu", "Yunpeng Liu", "Xiaofang Che", "Ling Xu"], "journal": "Science progress", "year": 2021, "abstract": "Immune cells have emerged as key regulators in the occurrence and development of multiple tumor types. However, it is unclear whether immune-related genes (IRGs) and the tumor immune microenvironment can predict prognosis for patients with gastric cancer (GC). The mRNA expression data in GC tissues (n = 368) were obtained from The Cancer Genome Atlas (TCGA) database. Differentially expressed IRGs in patients with GC were determined using a computational difference algorithm. A prognostic signature was constructed using COX regression and random survival forest (RSF) analyses. In addition, datasets related to \"gemcitabine resistance\" and \"trastuzumab resistance\" (GSE58118 and GSE77346) were obtained for GEO database, and DEGs associated with drug-resistance were screened. Then, we analyzed correlations between gene expression and cancer immune infiltrates via Tumor Immune Estimation Resource (TIMER) site. The cBioportal database was used to analyze drug-resistant gene mutation status and survival. One hundred and fifty-five differentially expressed IRGs were screened between GC and normal tissues, and a prognostic signature consisting of four IRGs (NRP1, PPP3R1, IL17RA, and FGF16) was closely related to the overall survival (OS). According to cutoff value of risk score, patients were divided into high-risk and low-risk group. Patients in the high-risk group had shorter OS compared to the low-risk group in both the training (p < 0.0001) and testing sets (p = 0.0021). In addition, we developed a 5-IRGs (LGR6, DKK1, TNFRSF1B, NRP1, and CXCR4) signature which may participate in drug resistance processes in GC. Survival analysis showed that patients with drug-resistant gene mutations had shorter OS (p = 0.0459) and DFS (p < 0.001). 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