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Updated: Aug 4, 2025

Modeling Osteosarcoma Using Li-Fraumeni Syndrome Patient-derived Induced Pluripotent Stem Cells
Published on: June 13, 2018
FKBP11 improves the malignant property of osteosarcoma cells and acts as a prognostic factor of osteosarcoma
Duo Zeng1,2, Jiayu Li1,2, Xuhui Yuan1,2
1Jiangxi Key Laboratory of Cancer Metastasis and Precision Treatment, Central Laboratory, The First Hospital of Nanchang, The Third Affiliated Hospital of Nanchang University, Nanchang, Jiangxi 330008, P.R. China.
Background:
Osteosarcoma has become the most common bone malignancy in adolescents. Although the clinical treatment of osteosarcoma has advanced considerably in recent years, the 5-year survival rate has not improved significantly. Recently, many studies have shown that mRNA has unique advantages as a target for drug therapy. Therefore, this study aimed to identify a new prognostic factor and provide a new target for the treatment of osteosarcoma to improve the prognosis of patients.
Methods And Results:
We selected prognostic genes that are closely associated with osteosarcoma clinical features by obtaining osteosarcoma patient information from the GTEx and TARGET databases, and then we developed a risk model. We detected the expression of FKBP11 in osteosarcoma by qRT-PCR, western blotting, and immunohistochemistry and performed CCK-8, Transwell, colony formation, and flow cytometry assays to reveal the regulatory role of FKBP11. We found that FKBP11 was highly expressed in osteosarcoma; silencing FKBP11 expression suppressed the invasion and migration of osteosarcoma cells, slowed cell proliferation, and promoted apoptosis. We also found that silencing the expression of FKBP11 led to inhibition of MEK/ERK phosphorylation.
Conclusions:
In conclusion, we validated that the prognostic factor FKBP11 is closely associated with osteosarcoma. Additionally, we identified a novel mechanism by which FKBP11 ameliorates the malignant properties of osteosarcoma cells through the MAPK pathway and serves as a prognostic factor in osteosarcoma. This study provides a new method for the treatment of osteosarcoma.
Insights
FKBP11 is highly expressed in osteosarcoma and promotes cancer progression. Silencing FKBP11 inhibits osteosarcoma cell invasion, migration, and proliferation, offering a potential new therapeutic target for this bone malignancy.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Osteosarcoma is a common adolescent bone cancer with stagnant survival rates despite treatment advances.
- Messenger RNA (mRNA) presents unique opportunities for targeted drug therapies.
- Identifying novel prognostic factors and therapeutic targets is crucial for improving osteosarcoma patient outcomes.
Purpose of the Study:
- To identify a new prognostic factor for osteosarcoma.
- To provide a novel therapeutic target for osteosarcoma treatment.
- To investigate the role of FKBP11 in osteosarcoma progression and its underlying mechanisms.
Main Methods:
- Utilized GTEx and TARGET databases to identify prognostic genes in osteosarcoma.
- Quantified FKBP11 expression using qRT-PCR, Western blotting, and immunohistochemistry.
- Assessed the functional role of FKBP11 in osteosarcoma cells via CCK-8, Transwell, colony formation, and flow cytometry assays.
Main Results:
- FKBP11 exhibited high expression in osteosarcoma tissues.
- Silencing FKBP11 suppressed osteosarcoma cell invasion, migration, proliferation, and induced apoptosis.
- FKBP11 knockdown inhibited MEK/ERK phosphorylation, implicating the MAPK pathway.
Conclusions:
- FKBP11 is a validated prognostic factor closely associated with osteosarcoma.
- FKBP11 promotes malignant properties of osteosarcoma cells via the MAPK pathway.
- This study offers a new therapeutic strategy targeting FKBP11 for osteosarcoma treatment.
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