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Updated: Feb 22, 2026

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma
Published on: April 12, 2019
Forkhead box C1 is targeted by microRNA-133b and promotes cell proliferation and migration in osteosarcoma
Lu Deng1, Tang Liu2, Beibei Zhang1
1Mental Health Institute, Second Xiangya Hospital of Central South University, Changsha, Hunan 410011, P.R. China.
Abstract:
Forkhead box C1 (FOXC1) has been demonstrated to act as an oncogene in a number of malignant tumors, though its underlying mechanism of action in osteosarcoma (OS) remains unknown. The present study evaluated the expression and regulatory role of FOXC1 in OS. Reverse transcription-quantitative polymerase chain reaction and western blot data indicated that FOXC1 was significantly upregulated in OS tissues and cell lines when compared with adjacent non-tumor tissues (P<0.001) and normal human osteoblast cells (P<0.01), respectively. Moreover, levels of FOXC1 expression were significantly higher in OS at advanced clinical stage (III-IV) when compared with that at low clinical stage (I-II; P<0.001). Knockdown of FOXC1 expression caused a significant decrease in the proliferation and migration of OS U2OS cells (P<0.01), while overexpression of FOXC1 significantly promoted U2OS cell proliferation and migration (P<0.01), relative to control U2OS cells. Furthermore, FOXC1 was identified as a direct target of microRNA (miR)-133b, a reported tumor-suppressive miR in OS. The protein expression of FOXC1 was negatively regulated by miR-133b in U2OS cells (P<0.01), and miR-133b expression was inversely correlated with FOXC1 expression in OS. In conclusion, the present study demonstrated that FOXC1, targeted by miR-133b, may promote cell proliferation and migration in OS. Thus, FOXC1 may be a potential therapeutic target in the treatment of OS.
Insights
Forkhead box C1 (FOXC1) promotes osteosarcoma (OS) cell growth and migration. This oncogene is upregulated in OS and targeted by the tumor-suppressive microRNA (miR)-133b, suggesting FOXC1 as a potential therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Forkhead box C1 (FOXC1) is an oncogene in various cancers.
- The role of FOXC1 in osteosarcoma (OS) pathogenesis is not well understood.
Purpose of the Study:
- To investigate the expression and regulatory role of FOXC1 in osteosarcoma.
- To explore the relationship between FOXC1 and microRNA-133b (miR-133b) in OS.
Main Methods:
- Quantitative reverse transcription-polymerase chain reaction (RT-qPCR) and Western blot analysis were used to assess FOXC1 expression.
- Cell proliferation and migration assays were performed following FOXC1 knockdown and overexpression.
- The interaction between miR-133b and FOXC1 was investigated.
Main Results:
- FOXC1 was significantly upregulated in OS tissues and cell lines compared to normal controls.
- FOXC1 expression levels correlated with advanced clinical stages of OS.
- FOXC1 knockdown inhibited OS cell proliferation and migration, while overexpression promoted these processes.
- FOXC1 was identified as a direct target of miR-133b, with inverse correlation observed between their expressions in OS.
Conclusions:
- FOXC1 acts as an oncogene in osteosarcoma, promoting cell proliferation and migration.
- FOXC1 is negatively regulated by the tumor-suppressive miR-133b in OS.
- FOXC1 represents a potential therapeutic target for osteosarcoma treatment.
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