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pmid:34323652

Development of a gene signature associated with iron metabolism in lung adenocarcinoma.

Junqi Qin · Zhanyu Xu · Kun Deng · Fanglu Qin · Jiangbo Wei · Liqiang Yuan · Yu Sun · Tiaozhan Zheng · Shikang Li

Bioengineered · 2021 doi:10.1080/21655979.2021.1954840

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complete

Experiment

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pmid:34323652
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science-record
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2026-11-01T15:41:45Z
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paper object · 10 fields
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title
Development of a gene signature associated with iron metabolism in lung adenocarcinoma.
doi
10.1080/21655979.2021.1954840
pmid
34323652
authors array · 9 items
[0]
Junqi Qin
[1]
Zhanyu Xu
[2]
Kun Deng
[3]
Fanglu Qin
[4]
Jiangbo Wei
[5]
Liqiang Yuan
[6]
Yu Sun
[7]
Tiaozhan Zheng
[8]
Shikang Li
journal
Bioengineered
year
2021
abstract
There are few studies on the role of iron metabolism genes in predicting the prognosis of lung adenocarcinoma (LUAD). Therefore, our research aims to screen key genes and to establish a prognostic signature that can predict the overall survival rate of lung adenocarcinoma patients. RNA-Seq data and corresponding clinical materials of 594 adenocarcinoma patients from The Cancer Genome Atlas(TCGA) were downloaded. GSE42127 of Gene Expression Omnibus (GEO) database was further verified. The multi-gene prognostic signature was constructed by the Cox regression model of the Least Absolute Shrinkage and Selection Operator (LASSO). We constructed a prediction signature with 12 genes (HAVCR1, SPN, GAPDH, ANGPTL4, PRSS3, KRT8, LDHA, HMMR, SLC2A1, CYP24A1, LOXL2, TIMP1), and patients were split into high and low-risk groups. The survival graph results revealed that the survival prognosis between the high and low-risk groups was significantly different (TCGA: P < 0.001, GEO: P = 0.001). Univariate and multivariate Cox regression analysis confirmed that the risk value is a predictor of patient OS (P < 0.001). The area under the time-dependent ROC curve (AUC) indicated that our signature had a relatively high true positive rate when predicting the 1-year, 3-year, and 5-year OS of the TCGA cohort, which was 0.735, 0.711, and 0.601, respectively. In addition, immune-related pathways were highlighted in the functional enrichment analysis. In conclusion, we developed and verified a 12-gene prognostic signature, which may be help predict the prognosis of lung adenocarcinoma and offer a variety of targeted options for the precise treatment of lung cancer.
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To determine the prognostic factors of overall lung adenocarcinoma survival, we carried out univariate and multivariate Cox regression analysis.
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sections[14] "Analysis of independent prognostic potency of 12-gene signature" paragraph 2
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To determine the prognostic factors of overall lung adenocarcinoma survival, we carried out univariate and multivariate Cox regression analysis.
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These data were freely available in The Cancer Genome Atlas (TCGA, https://portal.gdc.cancer.gov/), Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/) and Gene Cards (https://www.genecards.org/). These data are available from the corresponding author upon reasonable request. All data within the article and supplementary files are available for publish. All the raw data is publicly available.
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sections[24] "Availability of data and material" paragraph 2
quote
These data were freely available in The Cancer Genome Atlas (TCGA, https://portal.gdc.cancer.gov/), Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/) and Gene Cards (https://www.genecards.org/). These data are available from the corresponding author upon reasonable request. All data within the article and supplementary files are available for publish. All the raw data is publicly available.
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Expression data for non-small-cell lung cancer
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Identification of iron metabolism DEGs in LUAD
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Table 1.
caption
Clinical characteristics of the lung cancer patients used in this study
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GSE42127 (n, %)
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109 (83.2%)
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Identification of iron metabolism DEGs in LUAD
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Table 2.
caption
Univariate Cox analysis results of TCGA cohort-46 candidate genes
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0.003
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[0]
KRT19
[1]
1.001
[2]
1
[3]
1.001
[4]
0.004
[25] array · 5 items
[0]
GAPDH
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1.001
[2]
1
[3]
1.001
[4]
<0.001
[26] array · 5 items
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KPNA2
[1]
1.012
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1.006
[3]
1.017
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ANGPTL4
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1.009
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1.004
[3]
1.013
[4]
<0.001
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1.034
[2]
1.016
[3]
1.052
[4]
<0.001
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PRSS3
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1.024
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1.009
[3]
1.04
[4]
0.002
[30] array · 5 items
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KRT8
[1]
1.001
[2]
1.001
[3]
1.002
[4]
<0.001
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LDHA
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1.005
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1.003
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1.006
[4]
<0.001
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HMMR
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1.075
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1.041
[3]
1.11
[4]
<0.001
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ABCC2
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1.019
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1.007
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1.031
[4]
0.001
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CDKN3
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1.039
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1.013
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1.066
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0.003
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1.01
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1.007
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1.012
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1.035
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1.017
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1.053
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0.763
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0.63
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0.923
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1.009
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1.002
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1.016
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0.008
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0.96
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0.932
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0.99
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0.009
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1.003
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1.001
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1.004
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0.002
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1.003
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1.002
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1.005
[4]
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LOXL2
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1.02
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1.014
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1.027
[4]
<0.001
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TIMP1
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1.001
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1
[3]
1.002
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0.001
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1.002
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1.001
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1.003
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0.002
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1.012
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1.061
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0.003
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1.011
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1.004
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1.019
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0.001
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Univariate and multivariate Cox analysis of the 12-gene prognostic signature and clinical risk factors
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Analysis of independent prognostic potency of 12-gene signature
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Table 3.
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Univariate and multivariate Cox analysis of the 12-gene prognostic signature and clinical risk factors
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0.978–1.015
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0.718
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1.014
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1
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0.694–1.441
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1
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0.85
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0.585 − 1.235
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0.394
[5] array · 7 items
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1.648
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1.396–1.946
[3]
<0.001
[4]
1.921
[5]
1.154 − 3.198
[6]
0.012
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1.6
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1.285–1.994
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<0.001
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1.009
[5]
0.785 − 1.296
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0.946
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0.959–3.187
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0.068
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0.368
[5]
0.095 − 1.423
[6]
0.147
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1.787
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1.455–2.195
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<0.001
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0.943
[5]
0.603 − 1.476
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0.798
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Risk Score
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3.982
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3.313
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2.273 − 4.827
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HR (95% CI)
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1.01
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0.561
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0.407
[13] array · 7 items
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1.905
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0.994 − 3.650
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0.052
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1.23
[5]
0.616 − 2.454
[6]
0.557
[14] array · 7 items
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1.652
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1.144 − 2.387
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0.007
[4]
1.568
[5]
1.052 − 2.337
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0.027
[15] array · 7 items
[0]
RiskScore
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82.97
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10.025 − 686.710
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<0.001
[4]
84.063
[5]
7.882 − 896.502
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<0.001
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asset:data:geo:GSE42127 not downloaded
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To determine the prognostic factors of overall lung adenocarcinoma survival, we carried out univariate and multivariate Cox regression analysis.
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Automated Assays Laravel application and simulated adapters
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cox_ph
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The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards.
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GSE42127
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These data were freely available in The Cancer Genome Atlas (TCGA, https://portal.gdc.cancer.gov/), Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/) and Gene Cards (https://www.genecards.org/). These data are available from the corresponding author upon reasonable request. All data within the article and supplementary files are available for publish. All the raw data is publicly available.
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The paper names GSE42127 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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To determine the prognostic factors of overall lung adenocarcinoma survival, we carried out univariate and multivariate Cox regression analysis.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:34323652", "kind": "science-record", "revision": 7, "content_hash": "sha256:6747e79b0c6f1b96a24222ff0a188754bc3c690c1d9be151d64430c53c35631c", "created_at": "2026-11-01T15:41:45Z", "updated_at": "2026-11-01T22:04:20Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Development of a gene signature associated with iron metabolism in lung adenocarcinoma.", "doi": "10.1080/21655979.2021.1954840", "pmid": "34323652", "authors": ["Junqi Qin", "Zhanyu Xu", "Kun Deng", "Fanglu Qin", "Jiangbo Wei", "Liqiang Yuan", "Yu Sun", "Tiaozhan Zheng", "Shikang Li"], "journal": "Bioengineered", "year": 2021, "abstract": "There are few studies on the role of iron metabolism genes in predicting the prognosis of lung adenocarcinoma (LUAD). Therefore, our research aims to screen key genes and to establish a prognostic signature that can predict the overall survival rate of lung adenocarcinoma patients. RNA-Seq data and corresponding clinical materials of 594 adenocarcinoma patients from The Cancer Genome Atlas(TCGA) were downloaded. GSE42127 of Gene Expression Omnibus (GEO) database was further verified. The multi-gene prognostic signature was constructed by the Cox regression model of the Least Absolute Shrinkage and Selection Operator (LASSO). We constructed a prediction signature with 12 genes (HAVCR1, SPN, GAPDH, ANGPTL4, PRSS3, KRT8, LDHA, HMMR, SLC2A1, CYP24A1, LOXL2, TIMP1), and patients were split into high and low-risk groups. The survival graph results revealed that the survival prognosis between the high and low-risk groups was significantly different (TCGA: P < 0.001, GEO: P = 0.001). Univariate and multivariate Cox regression analysis confirmed that the risk value is a predictor of patient OS (P < 0.001). The area under the time-dependent ROC curve (AUC) indicated that our signature had a relatively high true positive rate when predicting the 1-year, 3-year, and 5-year OS of the TCGA cohort, which was 0.735, 0.711, and 0.601, respectively. In addition, immune-related pathways were highlighted in the functional enrichment analysis. 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