Title | Identification of novel prognostic biomarkers for osteosarcoma: a bioinformatics analysis of differentially expressed genes in the mesenchymal stem cells from single-cell sequencing data set |
Author | |
Corresponding Author | Xia, Jinquan; Yang, Shucai |
Publication Years | 2022-10-01
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DOI | |
Source Title | |
ISSN | 2218-676X
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EISSN | 2219-6803
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Volume | 11Issue:10 |
Abstract | Background: Mesenchymal stem cells (MSCs) play a crucial role in osteosarcoma (OS) growth and progression. This study conducted a bioinformatics analysis of a single-cell ribonucleic acid sequencing data set and explored the MSC-specific differentially expressed genes (DEGs) in advanced OS.Methods: MSC-specific DEGs from GSE152048 was extracted using Seurat R package. These DEGs were then subjected to the functional analysis, and several key genes were further identified and underwent a prognosis analysis.Results: A total of 234 upregulated and 280 downregulated DEGs were identified between the MSCs and other cells, and a total of 188 upregulated and 158 downregulated DEGs were identified between the MSCs and osteoblastic cells. The Gene Ontology (GO) functional analysis showed that the specific DEGs between the MSCs and osteoblastic cells were enriched in GO terms such as "collagen catabolic process", "positive regulation of pathway-restricted SMAD protein phosphorylation", "osteoblast differentiation", "regulation of release of cytochrome c from mitochondria" and "interleukin-1 production". The specific DEGs between the MSCs and osteoblastic cells were subjected to a protein-protein interaction network analysis. Further, a survival analysis of 20 genes with combined scores >0.94 revealed that the low expression of ANXA1 (annexin A1) and TPM1 (tropomyosin 1) was associated with the shorter overall survival of OS patients, while the high expression of FDPS (farnesyl pyrophosphate synthase), IFITM5 (interferon-induced transmembrane protein 5), FKBP11 (FKBP prolyl isomerase 11), SP7, and SQLE (squalene epoxidase) was associated with the shorter overall survival of OS patients. In a further analysis, we compared the expression of ANXA1, FDPS, IFITM5, FKBP11, SP7, SQLE, and TPM1 between the MSCs and high-grade OS cells. Further validation studies using the GSE42352 data set revealed thatANXA1, FKBP11, SP7, and TPM1 were more upregulated in the MSCs than the high-grade OS cells, while FDPS, IFITM5, and SQLE were more downregulated in the MSCs than the high-grade OS cells. Conclusions: Our bioinformatics analysis revealed 7 hub genes derived from the specific DEGs between the MSCs and osteoblastic cells. The 7 hub genes may serve as potential prognostic biomarkers for patients with OS. |
Keywords | |
URL | [Source Record] |
Indexed By | |
Language | English
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SUSTech Authorship | Others
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Funding Project | [202060]
; [B2021161]
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WOS Research Area | Oncology
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WOS Subject | Oncology
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WOS Accession No | WOS:000878572000010
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Publisher | |
Data Source | Web of Science
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Citation statistics |
Cited Times [WOS]:2
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Document Type | Journal Article |
Identifier | http://kc.sustech.edu.cn/handle/2SGJ60CL/412163 |
Department | Shenzhen People's Hospital |
Affiliation | 1.Third Peoples Hosp Shenzhen, Dept Orthopaed, Shenzhen, Peoples R China 2.Jinan Univ, Shenzhen Peoples Hosp, Dept Orthopaed, Clin Med Coll 2, Shenzhen, Peoples R China 3.Southern Univ Sci & Technol, Affiliated Hosp 1, Shenzhen, Peoples R China 4.Jinan Univ, Shenzhen Peoples Hosp, Dept Hand & Microvasscular Surg, Clin Med Coll 2, Shenzhen, Peoples R China 5.Southern Univ Sci & Technol, Affiliated Hosp 1, Shenzhen, Peoples R China 6.Nanjing Med Univ, Dept Orthopaed, Affiliated Huaian Peoples Hosp 1, Huaian, Peoples R China 7.Southern Med Univ, Pingshan Dist Peoples Hosp Shenzhen, Dept Clin Lab, Pingshan Gen Hosp, Shenzhen, Peoples R China 8.Southern Med Univ, Pingshan Dist Peoples Hosp Shenzhen, Dept Clin Lab, Pingshan Gen Hosp, Shenzhen 518000, Peoples R China 9.Third Peoples Hosp Shenzhen, Dept Orthopaed, Shenzhen 518000, Peoples R China |
Recommended Citation GB/T 7714 |
Jiang, Haoli,Du, Haoyuan,Liu, Yingnan,et al. Identification of novel prognostic biomarkers for osteosarcoma: a bioinformatics analysis of differentially expressed genes in the mesenchymal stem cells from single-cell sequencing data set[J]. Translational Cancer Research,2022,11(10).
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APA |
Jiang, Haoli,Du, Haoyuan,Liu, Yingnan,Tian, Xiao,Xia, Jinquan,&Yang, Shucai.(2022).Identification of novel prognostic biomarkers for osteosarcoma: a bioinformatics analysis of differentially expressed genes in the mesenchymal stem cells from single-cell sequencing data set.Translational Cancer Research,11(10).
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MLA |
Jiang, Haoli,et al."Identification of novel prognostic biomarkers for osteosarcoma: a bioinformatics analysis of differentially expressed genes in the mesenchymal stem cells from single-cell sequencing data set".Translational Cancer Research 11.10(2022).
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