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The overexpression of MRP4 is related to multidrug resistance in osteosarcoma cells
Zhonghui He, Beibei Hu, Lina Tang
1Department of Oncology, 6th People's Hospital Affiliated to Shanghai Jiaotong University, Shanghai 200233, China.
Abstract:
Doxorubicin (Adriamycin, ADM) is an antimitotic drug used in the treatment of a wide range of malignant tumors, including acute leukemia, lymphoma, osteosarcoma, breast cancer, and lung cancer. Multidrug resistance-associated proteins (MRPs) are members of a superfamily of ATP-binding cassette (ABC) transporters, which can transport various molecules across extra- and intra-cellular membranes. The aim of this study was to investigate whether there was a correlation between MRP4 and primary ADM resistance in osteosarcoma cells. In this paper, we chose the human osteosarcoma cell line MG63, ADM resistant cell line MG63/DOX, and the patient's primary cell GSF-0686. We checked the ADM sensitivity and cytotoxicity of all the three cells by cell proliferation assay. The intracellular drug concentrations were measured by using LC-MS/MS. We also examined MRP4 gene expression by RT-PCR and Western Blot. We found that the intracellular ADM concentration of the parent osteosarcoma cell line MG63 was higher than the ADM resistant osteosarcoma MG63/DOX cell line or the GSF-0686 cell after ADM treatment (P < 0.05). In addition, MRP4 mRNA and protein levels in ADM resistant osteosarcoma cells were higher than in MG63 cell (P < 0.05). Taking together, this work suggests that overexpression of MRP4 may confer ADM resistance in osteosarcoma cells.
Insights
Multidrug resistance-associated protein 4 (MRP4) may cause primary doxorubicin (ADM) resistance in osteosarcoma. Higher MRP4 levels in resistant cells correlate with lower intracellular ADM concentrations, suggesting MRP4 overexpression contributes to ADM resistance.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Doxorubicin (ADM) is a key antimitotic chemotherapy drug for various cancers.
- Multidrug resistance-associated proteins (MRPs) are ABC transporters linked to drug resistance.
- Primary resistance to ADM in osteosarcoma is a significant clinical challenge.
Purpose of the Study:
- To investigate the correlation between MRP4 and primary ADM resistance in osteosarcoma cells.
- To determine if MRP4 expression influences ADM sensitivity and intracellular drug levels.
Main Methods:
- Utilized human osteosarcoma cell lines (MG63, MG63/DOX) and primary patient cells (GSF-0686).
- Assessed ADM sensitivity and cytotoxicity via cell proliferation assays.
- Quantified intracellular ADM concentrations using LC-MS/MS.
- Examined MRP4 gene and protein expression using RT-PCR and Western Blot.
Main Results:
- Parental MG63 cells showed higher intracellular ADM concentrations than ADM-resistant cells (MG63/DOX, GSF-0686) post-treatment (P < 0.05).
- ADM-resistant cells exhibited significantly higher MRP4 mRNA and protein levels compared to MG63 cells (P < 0.05).
Conclusions:
- Overexpression of MRP4 is strongly suggested to confer primary ADM resistance in osteosarcoma.
- MRP4 may play a crucial role in the efflux of ADM from osteosarcoma cells, reducing drug efficacy.
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