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pmid:34329197

Identification of immune-related genes that predict prognosis and risk of bladder cancer: bioinformatics analysis of TCGA database.

Liqiang Guo · Qiong Wu · Zhen Ma · Mingzhen Yuan · Shengtian Zhao

Aging · 2021 doi:10.18632/aging.203333

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Identification of immune-related genes that predict prognosis and risk of bladder cancer: bioinformatics analysis of TCGA database.
doi
10.18632/aging.203333
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34329197
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Liqiang Guo
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Qiong Wu
[2]
Zhen Ma
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Mingzhen Yuan
[4]
Shengtian Zhao
journal
Aging
year
2021
abstract
BACKGROUND: Bladder cancer (BLCA) is the major tumor of the urinary system, and immune-related genes (IRGs) contribute significantly to its initiation and prognosis. RESULTS: A total of 51 prognostic IRGs significantly associated with overall survival were identified. Functional enrichment analysis revealed that these genes were actively involved in tumor-related functions and pathways. Using multivariate Cox regression analysis, we detected 11 optimal IRGs (ADIPOQ, PPY, NAMPT, TAP1, AHNAK, OLR1, PDGFRA, IL34, MMP9, RAC3, and SH3BP2). We validated the prognostic value of this signature in two validation cohorts: GSE13507 (n = 165) and GSE32894 (n = 224). Furthermore, we performed a western blot and found that the expression of these IRGs matched their mRNA expression in TCGA. Moreover, correlations between risk score and immune-cell infiltration indicated that the prognostic signature reflected infiltration by several types of immune cells. CONCLUSION: We identified and validated an 11-IRG-based risk signature that may be a reliable tool to evaluate the prognosis of BLCA patients and help to devise individualized immunotherapies. METHODS: Bioinformatics analysis was performed using TCGA and ImmPort databases. Cox regression was used to identify prognostic signatures. Two external GEO cohorts and western blotting of samples were performed to validate the IRG signature.
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Using multivariate Cox regression analysis, we detected 11 optimal IRGs (ADIPOQ, PPY, NAMPT, TAP1, AHNAK, OLR1, PDGFRA, IL34, MMP9, RAC3, and SH3BP2).
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Using multivariate Cox regression analysis, we detected 11 optimal IRGs (ADIPOQ, PPY, NAMPT, TAP1, AHNAK, OLR1, PDGFRA, IL34, MMP9, RAC3, and SH3BP2).
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Homo sapiens
title
A Molecular Taxonomy of Urothelial Carcinoma
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Univariate and multivariate Cox regression analyses of the cohort.
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section_index
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Independent prognostic value of the risk model of the cohort
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table object · 8 fields
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Table 1
caption
Univariate and multivariate Cox regression analyses of the cohort.
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[0] array · 3 items
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[1]
Univariate analysis
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Multivariate analysis
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95%CI
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HR
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Age
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1.029
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1.001-1.057
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0.04545
[4]
1.022
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0.993-1.052
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0.08953
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0.873
[5]
0.466-1.635
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0.67126
[4] array · 7 items
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1.863
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1.293-2.683
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0.00084
[4]
1.064
[5]
0.519-2.181
[6]
0.86637
[5] array · 7 items
[0]
T
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1.769
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1.193-2.622
[3]
0.00453
[4]
1.440
[5]
0.857-2.418
[6]
0.16832
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2.167
[2]
0.779-6.025
[3]
0.13822
[4]
0.907
[5]
0.274-3.000
[6]
0.87234
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1.573
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[3]
0.00121
[4]
1.227
[5]
0.728-2.068
[6]
0.44174
[8] array · 7 items
[0]
Risk score
[1]
1.398
[2]
1.265-1.544
[3]
4.33e-11
[4]
1.327
[5]
1.174-1.500
[6]
6.28e-06
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section[8]/table-wrap[1]#t1
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Relationships between prognostic model associated IRGs and clinical variables of patients with BLCA.
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PMC8386543
section_index
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section_title
Clinical application of the prognostic model
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label
Table 2
caption
Relationships between prognostic model associated IRGs and clinical variables of patients with BLCA.
rows array · 13 items
[0] array · 7 items
[0]
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[1]
Age (≤65/≥65) t(p)
[2]
Gender (Female/Male) t(p)
[3]
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[4]
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[5]
Tumor stage (T3&4/T1&2) t(p)
[6]
Lymph nodes (N1&2/N0) t(p)
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[0]
TAP1
[1]
1.132(0.259)
[2]
-0.104(0.917)
[3]
9.129(3.073e-13)
[4]
1.298(0.197)
[5]
1.006(0.316)
[6]
1.492(0.137)
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[0]
MMP9
[1]
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[2]
-0.888(0.376)
[3]
1.663(0.097)
[4]
-1.16(0.247)
[5]
-1.206(0.229)
[6]
-1.003(0.318)
[3] array · 7 items
[0]
ADIPOQ
[1]
-2.377(0.018)
[2]
1.167(0.246)
[3]
3.645(3.115e-04)
[4]
-0.339(0.735)
[5]
-0.662(0.509)
[6]
0.233(0.816)
[4] array · 7 items
[0]
PDGFRA
[1]
0.366(0.714)
[2]
1.446(0.150)
[3]
4.534(9.997e-05)
[4]
-3.645(3.199e-04)
[5]
-4.011(7.503e-05)
[6]
-1.492(0.137)
[5] array · 7 items
[0]
AHNAK
[1]
0.087(0.931)
[2]
0.901(0.369)
[3]
6.793(2.305e-07)
[4]
-3.435(7.172e-04)
[5]
-2.989(0.003)
[6]
-2.321(0.021)
[6] array · 7 items
[0]
OLR1
[1]
-0.016(0.987)
[2]
-0.369(0.712)
[3]
2.12(0.047)
[4]
-1.851(0.066)
[5]
-2.358(0.019)
[6]
-0.388(0.698)
[7] array · 7 items
[0]
RAC3
[1]
-1.8(0.073)
[2]
0.886(0.377)
[3]
4.227(1.542e-04)
[4]
-1.774(0.078)
[5]
-1.059(0.291)
[6]
-0.581(0.562)
[8] array · 7 items
[0]
IL34
[1]
-0.849(0.397)
[2]
0.352(0.725)
[3]
5.066(7.503e-07)
[4]
-1.974(0.049)
[5]
-2.444(0.015)
[6]
-2.053(0.042)
[9] array · 7 items
[0]
NAMPT
[1]
-0.698(0.486)
[2]
2.224(0.028)
[3]
4.5(1.488e-04)
[4]
-1.933(0.054)
[5]
-1.62(0.106)
[6]
0.682(0.495)
[10] array · 7 items
[0]
PPY
[1]
-1.385(0.167)
[2]
-0.174(0.862)
[3]
4.995(9.603e-07)
[4]
-1.524(0.128)
[5]
-1.795(0.074)
[6]
0.139(0.890)
[11] array · 7 items
[0]
SH3BP2
[1]
0.983(0.327)
[2]
-2.401(0.017)
[3]
-0.586(0.566)
[4]
2.384(0.019)
[5]
1.327(0.186)
[6]
1.974(0.049)
[12] array · 7 items
[0]
Risk Score
[1]
-1.426(0.155)
[2]
1.464(0.146)
[3]
5.272(2.433e-07)
[4]
-4.304(2.323e-05)
[5]
-3.926(1.101e-04)
[6]
-1.371(0.172)
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section[11]/table-wrap[1]#t2
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Using multivariate Cox regression analysis, we detected 11 optimal IRGs (ADIPOQ, PPY, NAMPT, TAP1, AHNAK, OLR1, PDGFRA, IL34, MMP9, RAC3, and SH3BP2).
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Clinical and transcriptome RNA-seq data of 433 BLCA samples, including 414 BLCA patients and 19 matched normal samples, downloaded from the TCGA cohort.
basis
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32894 (n = 224). Furthermore, we performed a western blot and found that the expression of these IRGs
[1]
tic signatures. Two external GEO cohorts and western blotting of samples were performed to validate the IR
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d data collection Clinical and transcriptome RNA-seq data of 433 BLCA samples, including 414 BLCA
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cal samples and data collection Clinical and transcriptome RNA-seq data of 433 BLCA samples, including
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Using multivariate Cox regression analysis, we detected 11 optimal IRGs (ADIPOQ, PPY, NAMPT, TAP1, AHNAK, OLR1, PDGFRA, IL34, MMP9, RAC3, and SH3BP2).
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:34329197", "kind": "science-record", "revision": 8, "content_hash": "sha256:42943e0e9a12e45518a6ee08210089767703515182dbfa7caa7866cfd2dbd67f", "created_at": "2026-11-01T15:41:45Z", "updated_at": "2026-11-01T22:04:21Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of immune-related genes that predict prognosis and risk of bladder cancer: bioinformatics analysis of TCGA database.", "doi": "10.18632/aging.203333", "pmid": "34329197", "authors": ["Liqiang Guo", "Qiong Wu", "Zhen Ma", "Mingzhen Yuan", "Shengtian Zhao"], "journal": "Aging", "year": 2021, "abstract": "BACKGROUND: Bladder cancer (BLCA) is the major tumor of the urinary system, and immune-related genes (IRGs) contribute significantly to its initiation and prognosis.\nRESULTS: A total of 51 prognostic IRGs significantly associated with overall survival were identified. Functional enrichment analysis revealed that these genes were actively involved in tumor-related functions and pathways. Using multivariate Cox regression analysis, we detected 11 optimal IRGs (ADIPOQ, PPY, NAMPT, TAP1, AHNAK, OLR1, PDGFRA, IL34, MMP9, RAC3, and SH3BP2). We validated the prognostic value of this signature in two validation cohorts: GSE13507 (n = 165) and GSE32894 (n = 224). Furthermore, we performed a western blot and found that the expression of these IRGs matched their mRNA expression in TCGA. Moreover, correlations between risk score and immune-cell infiltration indicated that the prognostic signature reflected infiltration by several types of immune cells.\nCONCLUSION: We identified and validated an 11-IRG-based risk signature that may be a reliable tool to evaluate the prognosis of BLCA patients and help to devise individualized immunotherapies.\nMETHODS: Bioinformatics analysis was performed using TCGA and ImmPort databases. 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Furthermore, we performed a western blot and found that the expression of these IRGs", "tic signatures. Two external GEO cohorts and western blotting of samples were performed to validate the IR"], "order_basis": "paper_text_order:778", "id": "assay:1"}, {"role": "data_generation", "definition_id": "rna_seq", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["d data collection Clinical and transcriptome RNA-seq data of 433 BLCA samples, including 414 BLCA", "cal samples and data collection Clinical and transcriptome RNA-seq data of 433 BLCA samples, including"], "order_basis": "paper_text_order:1550", "id": "assay:2"}, {"role": "analysis", "definition_id": "survival_analysis", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["cox_ph"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["Using multivariate Cox regression analysis, we detected 11 optimal IRGs (ADIPOQ, PPY, NAMPT, TAP1, AHNAK, OLR1, PDGFRA, IL34, MMP9, RAC3, and SH3BP2)."], "order_basis": "consumes_earlier_output", "id": "assay:3"}]}