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pmid:32087603

Development and validation of a RNA binding protein-associated prognostic model for lung adenocarcinoma.

Wei Li · Li-Na Gao · Pei-Pei Song · Chong-Ge You

Aging · 2020 doi:10.18632/aging.102828

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complete

Experiment

complete

Data

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Analysis

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title
Development and validation of a RNA binding protein-associated prognostic model for lung adenocarcinoma.
doi
10.18632/aging.102828
pmid
32087603
authors array · 4 items
[0]
Wei Li
[1]
Li-Na Gao
[2]
Pei-Pei Song
[3]
Chong-Ge You
journal
Aging
year
2020
abstract
RNA binding proteins (RBPs) dysregulation have been reported in various malignant tumors and associated with the occurrence and development of cancer. However, the role of RBPs in lung adenocarcinoma (LUAD) is poorly understood. We downloaded the RNA sequencing data of LUAD from the Cancer Genome Atlas (TCGA) database and determined the differently expressed RBPs between normal and cancer tissues. The study then systemically investigated the expression and prognostic value of these RBPs by a series of bioinformatics analysis. A total of 223 differently expressed RBPs were identified, including 101 up-regulated and 122 down-regulated RBPs. Eight RBPs (IGF2BP1, IFIT1B, PABPC1, TLR8, GAPDH, PIWIL4, RNPC3, and ZC3H12C) were identified as prognosis related hub gene and used to construct a prognostic model. Further analysis indicated that the patients in the high-risk subgroup had poor overall survival(OS) compared to those in low-risk subgroup based on the model. The area under the curve of the time-dependent receiver operator characteristic curve of the prognostic model are 0.775 in TCGA cohort and 0.814 in GSE31210 cohort, confirming a good prognostic model. We also established a nomogram based on eight RBPs mRNA and internal validation in the TCGA cohort, which displayed a favorable discriminating ability for lung adenocarcinoma.
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We downloaded the RNA-sequencing dataset of 59 normal lung tissue samples and 524 LUAD samples with corresponding clinical data from The Cancer Genome Atlas database (TCGA, https://portal.gdc.cancer.gov/).
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GO and KEGG pathway enrichment analysis of the differently expressed RBPs
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KEGG pathway and GO enrichment analysis of aberrantly expressed RBPs.
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structural molecule activity
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catalytic activity, acting on RNA
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Eight prognosis-associated hub RBPs identified by multivariate Cox regression analysis.
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Prognosis-related RBPs selecting
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Table 2
caption
Eight prognosis-associated hub RBPs identified by multivariate Cox regression analysis.
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The prognostic value of different clinical parameters.
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Construction of a nomogram based on the eight hub RBPs
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Table 3
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The prognostic value of different clinical parameters.
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“To identify the differently expressed genes between normal lung and LUAD tissue, we used the negative binomial distribution method.” “The Limma package (http://www.bioconductor.org/packages/release/bioc/html/limma.html) was applied to perform the analysis.” “The Limma package was based on the negative binomial distribution, it fits a generalized linear model for each gene and uses empirical Bayes shrinkage for dispersion and fold-change estimation.” “We downloaded the RNA-sequencing dataset of 59 normal lung tissue samples and 524 LUAD samples with corresponding clinical data from The Cancer Genome Atlas database (TCGA, https://portal.gdc.cancer.gov/).”
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We downloaded the RNA-sequencing dataset of 59 normal lung tissue samples and 524 LUAD samples with corresponding clinical data from The Cancer Genome Atlas database (TCGA, https://portal.gdc.cancer.gov/).
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We downloaded the RNA sequencing data of LUAD from the Cancer Genome Atlas (TCGA) database and determined the differently expressed RBPs between normal and cancer tissues. The study then systemically investigated the expression and prognostic value of these RBPs by a series of bioinformatics analysis. A total of 223 differently expressed RBPs were identified, including 101 up-regulated and 122 down-regulated RBPs. Eight RBPs (IGF2BP1, IFIT1B, PABPC1, TLR8, GAPDH, PIWIL4, RNPC3, and ZC3H12C) were identified as prognosis related hub gene and used to construct a prognostic model. Further analysis indicated that the patients in the high-risk subgroup had poor overall survival(OS) compared to those in low-risk subgroup based on the model. The area under the curve of the time-dependent receiver operator characteristic curve of the prognostic model are 0.775 in TCGA cohort and 0.814 in GSE31210 cohort, confirming a good prognostic model. 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