Related Experiment Video
Updated: Oct 15, 2025

Author Spotlight: RNA FISH for Locating lncRNA-SNHG6 in Osteosarcoma Cells
Published on: June 16, 2023
Identification of Conserved Pappalysin 1-Derived Circular RNA-Mediated Competing Endogenous RNA in Osteosarcoma
Guang-Fu Ming1, Bo-Hua Gao1, Peng Chen1
1Department of Orthopedics, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University), Haikou, China.
Abstract:
The etiology of osteosarcoma (OS) is complex and not fully understood till now. This study aimed to identify the miRNAs, circRNAs, and genes (mRNAs) that are differentially expressed in OS cell lines to investigate the mechanism of circRNA-associated competing endogenous RNAs (ceRNAs) in OS. Microarray datasets reporting mRNA (GSE70414), miRNA (GSE70367), and circRNA changes (GSE96964) in human OS cell lines were downloaded, differentially expressed (DE) RNAs were identified, and DEmRNAs were used for the annotation of Gene Ontology (GO) biological processes (BP), and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. The mechanisms of DEcircRNA-mediated ceRNAs were identified in a step-by-step process. A total of 326 DEmRNAs, 45 DEmiRNAs, and 110 DEcircRNAs were identified from 3 datasets. The DEmRNAs were associated with GO BP terms, including cholesterol biosynthetic process, angiogenesis, extracellular matrix organization and KEGG pathways, including p53 signaling pathway and biosynthesis of antibiotics. The final ceRNA network consisted of 8 DEcircRNAs, including 5 pappalysin (PAPPA) 1-derived DEcircRNAs (hsa_circ_0005456, hsa_circ_0088209, hsa_circ_0002052, hsa_circ_0088214 and has_circ_0008792, all downregulated), 3 DEmiRNAs (hsa-miR-760, hsa-miR-4665-5p and hsa-miR-4539, all upregulated), and downregulated genes (including MMP13 and HMOX1). The ceRNA regulation network of OS was built, which played important roles in the pathogenesis of OS and might be of great importance in therapy.
Insights
This study identifies key microRNAs (miRNAs), circular RNAs (circRNAs), and messenger RNAs (mRNAs) involved in osteosarcoma (OS) pathogenesis. The findings reveal a competing endogenous RNA (ceRNA) network crucial for OS development and potential therapeutic targets.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Osteosarcoma (OS) etiology is complex and not fully understood.
- MicroRNAs (miRNAs), circular RNAs (circRNAs), and messenger RNAs (mRNAs) play roles in cancer development.
- Understanding regulatory networks like competing endogenous RNAs (ceRNAs) is vital for OS research.
Purpose of the Study:
- To identify differentially expressed miRNAs, circRNAs, and mRNAs in osteosarcoma (OS) cell lines.
- To investigate the mechanism of circRNA-associated competing endogenous RNAs (ceRNAs) in OS.
- To build a ceRNA regulatory network for OS pathogenesis.
Main Methods:
- Downloaded and analyzed microarray datasets for mRNA, miRNA, and circRNA expression in human OS cell lines.
- Identified differentially expressed RNAs (DE RNAs).
- Annotated DE mRNAs for Gene Ontology (GO) biological processes and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. Identified DEcircRNA-mediated ceRNA mechanisms.
Main Results:
- Identified 326 DEmRNAs, 45 DEmiRNAs, and 110 DEcircRNAs.
- DEmRNAs associated with GO BP terms like angiogenesis and KEGG pathways including the p53 signaling pathway.
- Constructed a ceRNA network involving 8 DEcircRNAs, 3 DEmiRNAs, and downregulated genes (MMP13, HMOX1).
Conclusions:
- A circRNA-ceRNA regulatory network in osteosarcoma was successfully built.
- This network plays significant roles in OS pathogenesis.
- The identified network components may represent important therapeutic targets for osteosarcoma.
Related Concept Videos
Experimental RNAi
Rous Sarcoma Virus (RSV) and Cancer
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...

