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Updated: Jun 29, 2025

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
Published on: April 7, 2017
Circ_0049271 targets the miR-1197/PTRF axis to attenuate the malignancy of osteosarcoma
Yixin Wen1,1, Feng Xu1,1, Hui Zhang1
1Orthopaedics Department, Fifth Hospital of Wuhan, Wuhan, Hubei, China.
Background:
Circular RNAs (circRNAs) perform key regulatory functions in osteosarcoma (OS) tumorigenesis. In this study, we aimed to explore the detailed action mechanisms of circ_0049271 in OS progression.
Methods:
Cell colony formation, cell counting kit-8, and transwell assays were performed to assess the proliferation and invasion of OS cells. Quantitative reverse transcription-polymerase chain reaction and western blotting were used to determine the expression levels of polymerase 1 and transcript release factor (PTRF), microRNA (miR)-1197, and circ_0049271 in OS cells. Furthermore, RNA immunoprecipitation and dual luciferase assays were conducted to explore the targeted relationships among PTRF, miR-1197, and circ_0049271. Finally, a tumor formation assay was conducted to determine the effects of circ_0049271 on in vivo tumor growth in mice.
Results:
High expression levels of miR-1197 and low levels of circ_0049271 and PTRF were observed in OS cells. circ _0049271 targeted miR-1197 to mediate PTRF expression. Moreover, the proliferation and invasion of OS cells were repressed by circ_0049271 or PTRF overexpression and increased by miR-1197 upregulation. Enforced circ_0049271 also impeded tumor growth in vivo. Upregulation of miR-1197 reversed the antitumor effects of circ_0049271 on OS progression in vitro; however, PTRF overexpression attenuated the cancer-promoting effects of miR-1197 on OS in vitro.
Conclusions:
Our findings revealed that circ_0049271 targeted the miR-1197/PTRF axis to attenuate the malignancy of OS, suggesting a potential target for its clinical treatment.
Insights
Circular RNA circ_0049271 inhibits osteosarcoma progression by targeting microRNA-1197 to regulate polymerase 1 and transcript release factor (PTRF). This suggests circ_0049271 as a potential therapeutic target for osteosarcoma.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Circular RNAs (circRNAs) play crucial roles in the development of osteosarcoma (OS).
- Understanding the specific mechanisms of circRNAs in OS is vital for developing new treatments.
Purpose of the Study:
- To investigate the functional role and underlying mechanisms of circ_0049271 in osteosarcoma progression.
- To explore the regulatory relationship between circ_0049271, microRNA-1197 (miR-1197), and polymerase 1 and transcript release factor (PTRF) in OS.
Main Methods:
- Cellular assays (colony formation, CCK-8, Transwell) were used to evaluate OS cell proliferation and invasion.
- Quantitative reverse transcription-polymerase chain reaction and western blotting assessed expression levels of key molecules.
- RNA immunoprecipitation and dual luciferase assays determined molecular interactions.
- In vivo tumor formation assays evaluated the effect of circ_0049271 on tumor growth.
Main Results:
- Osteosarcoma cells exhibited high miR-1197 expression and low circ_0049271 and PTRF levels.
- circ_0049271 directly targeted miR-1197, thereby regulating PTRF expression.
- Overexpression of circ_0049271 or PTRF suppressed OS cell proliferation and invasion, while miR-1197 upregulation promoted these processes.
- circ_0049271 inhibited tumor growth in vivo, and PTRF overexpression counteracted the oncogenic effects of miR-1197.
Conclusions:
- circ_0049271 functions as a tumor suppressor in osteosarcoma by targeting the miR-1197/PTRF axis.
- This circRNA-mediated pathway offers a potential therapeutic strategy for osteosarcoma treatment.
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