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pmid:33048468

Identification of a prognostic gene signature based on an immunogenomic landscape analysis of bladder cancer.

Yongwen Luo · Liang Chen · Qiang Zhou · Yaoyi Xiong · Gang Wang · Xuefeng Liu · Yu Xiao · Lingao Ju · Xinghuan Wang

Journal of cellular and molecular medicine · 2020 doi:10.1111/jcmm.15960

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Experiment

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Data

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pmid:33048468
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2026-11-01T15:41:13Z
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paper object · 10 fields
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title
Identification of a prognostic gene signature based on an immunogenomic landscape analysis of bladder cancer.
doi
10.1111/jcmm.15960
pmid
33048468
authors array · 9 items
[0]
Yongwen Luo
[1]
Liang Chen
[2]
Qiang Zhou
[3]
Yaoyi Xiong
[4]
Gang Wang
[5]
Xuefeng Liu
[6]
Yu Xiao
[7]
Lingao Ju
[8]
Xinghuan Wang
journal
Journal of cellular and molecular medicine
year
2020
abstract
Cancer immune plays a critical role in cancer progression. Tumour immunology and immunotherapy are one of the exciting areas in bladder cancer research. In this study, we aimed to develop an immune-related gene signature to improve the prognostic prediction of bladder cancer. Firstly, we identified 392 differentially expressed immune-related genes (IRGs) based on TCGA and ImmPort databases. Functional enrichment analysis revealed that these genes were enriched in inflammatory and immune-related pathways, including in 'regulation of signaling receptor activity', 'cytokine-cytokine receptor interaction' and 'GPCR ligand binding'. Then, we separated all samples in TCGA data set into the training cohort and the testing cohort in a ratio of 3:1 randomly. Data set GSE13507 was set as the validation cohort. We constructed a prognostic six-IRG signature with LASSO Cox regression in the training cohort, including AHNAK, OAS1, APOBEC3H, SCG2, CTSE and KIR2DS4. Six IRGs reflected the microenvironment of bladder cancer, especially immune cell infiltration. The prognostic value of six-IRG signature was further validated in the testing cohort and the validation cohort. The results of multivariable Cox regression and subgroup analysis revealed that six-IRG signature was a clinically independent prognostic factor for bladder cancer patients. Further, we constructed a nomogram based on six-IRG signature and other clinicopathological risk factors, and it performed well in predict patients' survival. Finally, we found six-IRG signature showed significant difference in different molecular subtypes of bladder cancer. In conclusions, our research provided a novel immune-related gene signature to estimate prognosis for patients' survival with bladder cancer.
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To explore whether six‐IRG signature was a clinically independent prognostic factor in bladder cancer patients, we performed univariable and multivariable Cox regression analyses in TCGA data set.
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sections[18] "Validation of the six‐IRG signature as an independent prognostic factor" paragraph 2
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To explore whether six‐IRG signature was a clinically independent prognostic factor in bladder cancer patients, we performed univariable and multivariable Cox regression analyses in TCGA data set.
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The data that support the findings of this study are openly available in The Cancer Genome Atlas (TCGA) data portal (https://tcga‐data.nci.nih.gov/tcga/), Gene Expression Omnibus (GEO) database (http://www.ncbi.nlm.nih.gov/geo/) and ImmPort data portal ( https://www.immport.org ).
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sections[31] "DATA AVAILABILITY STATEMENT" paragraph 2
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The data that support the findings of this study are openly available in The Cancer Genome Atlas (TCGA) data portal (https://tcga‐data.nci.nih.gov/tcga/), Gene Expression Omnibus (GEO) database (http://www.ncbi.nlm.nih.gov/geo/) and ImmPort data portal ( https://www.immport.org ).
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The data that support the findings of this study are openly available in The Cancer Genome Atlas (TCGA) data portal (https://tcga‐data.nci.nih.gov/tcga/), Gene Expression Omnibus (GEO) database (http://www.ncbi.nlm.nih.gov/geo/) and ImmPort data portal ( https://www.immport.org ).
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title
Predective Value of Prognosis-Related Gene Expression Study in Primary Bladder Cancer
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Association of six‐IRG signature with clinicopathological characteristics
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Association of six‐IRG signature with patients' clinicopathological characteristics
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Association of six‐IRG signature with clinicopathological characteristics
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The data that support the findings of this study are openly available in The Cancer Genome Atlas (TCGA) data portal (https://tcga‐data.nci.nih.gov/tcga/), Gene Expression Omnibus (GEO) database (http://www.ncbi.nlm.nih.gov/geo/) and ImmPort data portal ( https://www.immport.org ).
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e were collected from TCGA database. All the patients were assigned to the high‐risk group and the low‐risk grou
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To explore whether six‐IRG signature was a clinically independent prognostic factor in bladder cancer patients, we performed univariable and multivariable Cox regression analyses in TCGA data set.
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Complete file
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In this study, we aimed to develop an immune-related gene signature to improve the prognostic prediction of bladder cancer. Firstly, we identified 392 differentially expressed immune-related genes (IRGs) based on TCGA and ImmPort databases. Functional enrichment analysis revealed that these genes were enriched in inflammatory and immune-related pathways, including in 'regulation of signaling receptor activity', 'cytokine-cytokine receptor interaction' and 'GPCR ligand binding'. Then, we separated all samples in TCGA data set into the training cohort and the testing cohort in a ratio of 3:1 randomly. Data set GSE13507 was set as the validation cohort. We constructed a prognostic six-IRG signature with LASSO Cox regression in the training cohort, including AHNAK, OAS1, APOBEC3H, SCG2, CTSE and KIR2DS4. Six IRGs reflected the microenvironment of bladder cancer, especially immune cell infiltration. The prognostic value of six-IRG signature was further validated in the testing cohort and the validation cohort. The results of multivariable Cox regression and subgroup analysis revealed that six-IRG signature was a clinically independent prognostic factor for bladder cancer patients. Further, we constructed a nomogram based on six-IRG signature and other clinicopathological risk factors, and it performed well in predict patients' survival. Finally, we found six-IRG signature showed significant difference in different molecular subtypes of bladder cancer. 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