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Published on: May 3, 2021
RAIDD expression is impaired in multidrug resistant osteosarcoma cell lines
Cao Yang1, Francis J Hornicek, Kirkham B Wood
1Department of Orthopaedic Surgery, Massachusetts General Hospital, Boston, MA 02114, USA.
Purpose:
To identify the apoptosis genes involved in the multidrug resistant phenotype of osteosarcoma.
Methods:
Multidrug resistant human osteosarcoma cell line (U-2 OS MR) and a drug sensitive parental cell line (U-2 OS) were both treated with paclitaxel and analyzed by the gene array containing 96 apoptosis associated genes. The different expression of the special apoptosis associated genes were further analyzed by Western blot in the multidrug resistant osteosarcoma cell lines (U-2 OS MR, KH OS R2) and the drug sensitive parental cell lines (U-2 OS, KH OS). One of the disregulated gene, RAIDD, was transfected into the multidrug resistant osteosarcoma cells for functional studies.
Results:
RAIDD showed signs of significant expression in the U-2 OS cells after being treated with paclitaxel (P < 0.01). However, the induction of RAIDD did not occur in U-2 OS MR cells (P = 0.2). Subsequent analysis by Western blot confirmed the deficiency of the expression of RAIDD protein in U-2 OS MR. On the contrary, the expression of RAIDD could be significantly induced by paclitaxel and doxorubicin in U-2 OS cells as both time and dosage were deciding factors. It also demonstrated the cleavage of PARP associated with RAIDD expression in U-2 OS cells, but not however in U-2 OS MR cells after being treated with paclitaxel or doxorubicin. Similar results were found in osteosarcoma multidrug resistant cell line KH OS R2 and the drug sensitive parental cell line KH OS. Furthermore, over-expression of RAIDD in multidrug resistant cell lines could possibly reverse drug resistant phenotypes.
Conclusion:
This study indicate that impaired expression of RAIDD in drug induced apoptosis may play a role in the multidrug resistance of osteosarcoma cells.
Insights
Impaired RAIDD gene expression contributes to multidrug resistance in osteosarcoma. Restoring RAIDD may reverse this resistance, offering a potential therapeutic target for osteosarcoma treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Osteosarcoma is a primary bone cancer with a significant challenge in multidrug resistance.
- Understanding the genetic basis of multidrug resistance is crucial for developing effective treatments.
Purpose of the Study:
- To identify apoptosis-related genes contributing to the multidrug resistance phenotype in osteosarcoma.
- To investigate the role of the RAIDD gene in osteosarcoma multidrug resistance.
Main Methods:
- Gene array analysis of apoptosis-associated genes in multidrug-resistant (U-2 OS MR) and sensitive (U-2 OS) osteosarcoma cell lines treated with paclitaxel.
- Western blot analysis to confirm gene expression differences, focusing on the RAIDD gene.
- Functional studies involving transfection of the RAIDD gene into multidrug-resistant cells.
Main Results:
- RAIDD gene expression was significantly induced by paclitaxel in sensitive cells but not in resistant cells.
- Western blot confirmed a deficiency in RAIDD protein expression in multidrug-resistant osteosarcoma cell lines (U-2 OS MR, KH OS R2).
- Overexpression of RAIDD in resistant cells showed potential to reverse drug-resistant phenotypes and induced Poly (ADP-ribose) polymerase (PARP) cleavage.
Conclusions:
- Impaired expression of the RAIDD gene is implicated in the multidrug resistance of osteosarcoma.
- RAIDD deficiency in drug-induced apoptosis may be a key factor in osteosarcoma's resistance to chemotherapy.
- Targeting RAIDD expression could offer a novel therapeutic strategy for overcoming multidrug resistance in osteosarcoma.
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