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pmid:33754909

Identification of Prognostic RBPs in Osteosarcoma.

Bei Li · Long Fang · Baolong Wang · Zengkun Yang · Tingbao Zhao

Technology in cancer research & treatment · 2021 doi:10.1177/15330338211004918

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
Identification of Prognostic RBPs in Osteosarcoma.
doi
10.1177/15330338211004918
pmid
33754909
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Bei Li
[1]
Long Fang
[2]
Baolong Wang
[3]
Zengkun Yang
[4]
Tingbao Zhao
journal
Technology in cancer research & treatment
year
2021
abstract
Osteosarcoma often occurs in children and adolescents and causes poor prognosis. The role of RNA-binding proteins (RBPs) in malignant tumors has been elucidated in recent years. Our study aims to identify key RBPs in osteosarcoma that could be prognostic factors and treatment targets. GSE33382 dataset was downloaded from Gene Expression Omnibus (GEO) database. RBPs extraction and differential expression analysis was performed. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis were performed to explore the biological function of differential expression RBPs. Moreover, we constructed Protein-protein interaction (PPI) network and obtained key modules. Key RBPs were identified by univariate Cox regression analysis and multiple stepwise Cox regression analysis combined with the clinical information from Therapeutically Applicable Research to Generate Effective Treatments (TARGET) database. Risk score model was generated and validated by GSE16091 dataset. A total of 38 differential expression RBPs was identified. Go and KEGG results indicated these RBPs were significantly involved in ribosome biogenesis and mRNA surveillance pathway. COX regression analysis showed DDX24, DDX21, WARS and IGF2BP2 could be prognostic factors in osteosarcoma. Spearman's correlation analysis suggested that WARS might be important in osteosarcoma immune infiltration. In conclusion, DDX24, DDX21, WARS and IGF2BP2 might play key role in osteosarcoma, which could be therapuetic targets for osteosarcoma treatment.
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Then we used the limma package (https://www.bioconductor.org/packages/release/bioc/html/limma.html) in R 4.0.2 to identify differentially expressed RBPs between normal samples and tumor samples according to |log2 fold change (FC)| > 1 and adj. P < 0.05.
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Then we used the limma package (https://www.bioconductor.org/packages/release/bioc/html/limma.html) in R 4.0.2 to identify differentially expressed RBPs between normal samples and tumor samples according to |log2 fold change (FC)| > 1 and adj. P < 0.05.
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GO and KEGG Pathway Enrichment Analysis
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Then we used the limma package (https://www.bioconductor.org/packages/release/bioc/html/limma.html) in R 4.0.2 to identify differentially expressed RBPs between normal samples and tumor samples according to |log2 fold change (FC)| > 1 and adj. P < 0.05.
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sha256:d1fe3d26e2dacce01642db7013c00a5e1e5c401571acedb46580da67348efc80
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gaps array · 9 items
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asset:data:geo:GSE16091 licence not read
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asset:data:geo:GSE33382 licence not read
[3]
asset:data:geo:GSE33382 not downloaded
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method.reader_differs_from_extractor
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review.human_critique
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review.machine_critique
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1% streptomycin (100/mL). MG-63 and MNNG/HOS cell lines were cultured in Minimum Essential Medium (MEM) supplement
[1]
penicillin and 1% streptomycin (100/mL). All cell lines were cultured at 37°C, 5% CO2. Experiment Data Statistical
[2]
ture Collection (ATCC). hFOB 1.19 cells were cultured in complete growth medium consisting of a 1:1 m
[3]
(100/mL). MG-63 and MNNG/HOS cell lines were cultured in Minimum Essential Medium (MEM) supplemented
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paper_text_order:1747
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Then we used the limma package (https://www.bioconductor.org/packages/release/bioc/html/limma.html) in R 4.0.2 to identify differentially expressed RBPs between normal samples and tumor samples according to |log2 fold change (FC)| > 1 and adj. P < 0.05.
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Complete file
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