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Updated: Feb 24, 2026

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
Published on: April 7, 2017
RSF1 functions as an oncogene in osteosarcoma and is regulated by XIST/miR-193a-3p axis
Dapeng Wu1, Xingguo Nie2, Chao Ma2
1Department of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, Henan, China; Department of Orthopedics, The First Affiliated Hospital of Xinxiang Medical University, Weihui 453100, Henan, China.
Abstract:
RSF1 (HBXAP), is a member of ATP-dependent chromatin remodeling factor. Dysregulated RSF1 has been reported to be related to tumor progression. However, the function of RSF1 in osteosarcoma (OS) remains unclear. In this study, we showed that RSF1 expression was upregulated in OS cells. RSF1 inhibition suppressed OS cell proliferation and invasion. We further showed that MAPK/Erk signaling pathway was inactivated by RSF1 suppression. In addition, RSF1 was identified as a direct target of miR-193a-3p. Clinically, RSF1 was increased and associated with advanced clinical features and poor overall survival of OS patients. MiR-193a-3p expression was decreased and associated with advanced clinical features and poor overall survival of OS patients. In addition, we found that miR-193a-3p was negatively correlated with RSF1 expression in OS tissues. Moreover, our data showed that XIST could function as competing endogenous RNA to repress miR-193a-3p, which regulated its downstream target RSF1. In conclusion, our findings demonstrated that the XIST/miR-193a-3p/RSF1 axis might contribute to the progression and act as a therapeutic target of OS patients.
Insights
The XIST/miR-193a-3p/RSF1 axis promotes osteosarcoma (OS) progression. Inhibiting RSF1 or targeting this axis may offer new therapeutic strategies for OS patients.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- RSF1 (HBXAP) is an ATP-dependent chromatin remodeling factor implicated in tumor progression.
- The specific role of RSF1 in osteosarcoma (OS) pathogenesis is not well understood.
Purpose of the Study:
- To investigate the function of RSF1 in osteosarcoma.
- To elucidate the regulatory mechanism involving XIST, miR-193a-3p, and RSF1 in OS.
Main Methods:
- Analysis of RSF1 expression in OS cells and tissues.
- Assessment of RSF1 inhibition effects on OS cell proliferation and invasion.
- Investigation of the MAPK/Erk signaling pathway.
- Detection of RSF1 as a target of miR-193a-3p.
- Correlation analysis of XIST, miR-193a-3p, and RSF1 in OS tissues.
Main Results:
- RSF1 expression is upregulated in OS cells and associated with advanced clinical features and poor survival.
- RSF1 inhibition suppresses OS cell proliferation, invasion, and inactivates the MAPK/Erk pathway.
- RSF1 is a direct target of miR-193a-3p, which is downregulated in OS.
- XIST acts as a competing endogenous RNA (ceRNA) to repress miR-193a-3p, thereby regulating RSF1.
Conclusions:
- The XIST/miR-193a-3p/RSF1 regulatory axis plays a significant role in osteosarcoma progression.
- This axis represents a potential therapeutic target for osteosarcoma treatment.
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