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Published on: October 28, 2021
CircEIF4G2 Promotes Tumorigenesis and Progression of Osteosarcoma by Sponging miR-218
Erhu Lin1, Shuai Liu2, Wei Xiang2
1Spinal Surgery Department, Shenzhen People's Hospital, Shenzhen, Guangdong 518000, China.
Abstract:
Circular RNAs (circRNAs) play a key role in regulating the tumorigenesis and development of human cancers, including osteosarcoma (OS). Of note, the molecular mechanism underlying the progression of OS has remained largely unclear. The present study identified that a novel circRNA circEIF4G2 was upregulated in OS tissues and cells. Moreover, we constructed a circEIF4G2-mediated ceRNA network and revealed that circEIF4G2 was involved in regulating multiple cancer pathways, such as the EGFR signaling pathway, the PI3K-Akt signaling pathway, and the ErbB signaling pathway. Loss-of-function assays showed that circEIF4G2 knockdown significantly suppressed OS cell proliferation, migration, and invasion. Mechanically, we found that circEIF4G2 could directly bind to miR-218, and miR-218 mediated the effect of circEIF4G2 knockdown on OS progression. In conclusion, the present study showed that circEIF4G2 could be a potential biomarker for OS.
Insights
This study identifies circEIF4G2 as a novel circular RNA upregulated in osteosarcoma (OS). Knockdown of circEIF4G2 suppressed tumor progression by interacting with miR-218, suggesting its potential as an OS biomarker.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Circular RNAs (circRNAs) are implicated in human cancer development, including osteosarcoma (OS).
- The precise molecular mechanisms driving OS progression remain incompletely understood.
- Identifying novel regulatory elements is crucial for understanding OS pathogenesis.
Purpose of the Study:
- To investigate the role of a novel circRNA, circEIF4G2, in osteosarcoma.
- To elucidate the molecular mechanisms by which circEIF4G2 influences OS progression.
- To evaluate circEIF4G2 as a potential diagnostic biomarker for osteosarcoma.
Main Methods:
- Differential expression analysis of circEIF4G2 in OS tissues and cells.
- Construction of a circEIF4G2-mediated competing endogenous RNA (ceRNA) network.
- Loss-of-function experiments (siRNA-mediated knockdown) to assess circEIF4G2's impact on OS cells.
- Mechanistic investigation involving direct binding assays between circEIF4G2 and miR-218.
Main Results:
- circEIF4G2 was found to be significantly upregulated in osteosarcoma tissues and cell lines.
- circEIF4G2 knockdown markedly inhibited osteosarcoma cell proliferation, migration, and invasion.
- circEIF4G2 was demonstrated to directly bind to miR-218, with miR-218 mediating circEIF4G2's effects on OS progression.
- circEIF4G2 participates in regulating key cancer pathways, including EGFR, PI3K-Akt, and ErbB signaling.
Conclusions:
- circEIF4G2 plays a significant role in promoting osteosarcoma progression.
- The circEIF4G2/miR-218 axis is a key regulatory mechanism in osteosarcoma.
- circEIF4G2 holds promise as a potential biomarker for osteosarcoma diagnosis and prognosis.
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