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CD44 Contributes to the Regulation of MDR1 Protein and Doxorubicin Chemoresistance in Osteosarcoma
Monserrat Gerardo-Ramírez1, Friederike L Keggenhoff1, Vanessa Giam1
1Department of Medicine I, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.
Abstract:
Osteosarcoma is the most common type of pediatric bone tumor. Despite great advances in chemotherapy during the past decades, the survival rates of osteosarcoma patients remain unsatisfactory. Drug resistance is one of the main reasons, leading to treatment failure and poor prognosis. Previous reports correlated expression of cluster of differentiation 44 (CD44) with drug resistance and poor survival of osteosarcoma patients, however the underlying mechanisms are poorly defined. Here, we investigated the role of CD44 in the regulation of drug chemoresistance, using osteosarcoma cells isolated from mice carrying a mutation of the tumor suppressor neurofibromatosis type 2 (Nf2) gene. CD44 expression was knocked-down in the cells using CRISPR/Cas9 approach. Subsequently, CD44 isoforms and mutants were re-introduced to investigate CD44-dependent processes. Sensitivity to doxorubicin was analyzed in the osteosarcoma cells with modified CD44 expression by immunoblot, colony formation- and WST-1 assay. To dissect the molecular alterations induced by deletion of Cd44, RNA sequencing was performed on Cd44-positive and Cd44-negative primary osteosarcoma tissues isolated from Nf2-mutant mice. Subsequently, expression of candidate genes was evaluated by quantitative reverse transcription PCR (qRT-PCR). Our results indicate that CD44 increases the resistance of osteosarcoma cells to doxorubicin by up-regulating the levels of multidrug resistance (MDR) 1 protein expression, and suggest the role of proteolytically released CD44 intracellular domain, and hyaluronan interactions in this process. Moreover, high throughput sequencing analysis identified differential regulation of several apoptosis-related genes in Cd44-positive and -negative primary osteosarcomas, including p53 apoptosis effector related to PMP-22 (Perp). Deletion of Cd44 in osteosarcoma cells led to doxorubicin-dependent p53 activation and a profound increase in Perp mRNA expression. Overall, our results suggest that CD44 might be an important regulator of drug resistance and suggest that targeting CD44 can sensitize osteosarcoma to standard chemotherapy.
Insights
Cluster of differentiation 44 (CD44) enhances osteosarcoma chemoresistance by upregulating multidrug resistance protein 1. Targeting CD44 may sensitize pediatric bone tumors to chemotherapy.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Osteosarcoma, a common pediatric bone tumor, has unsatisfactory survival rates due to drug resistance.
- Cluster of differentiation 44 (CD44) is implicated in osteosarcoma drug resistance, but mechanisms are unclear.
Purpose of the Study:
- To investigate the role of CD44 in regulating chemoresistance in osteosarcoma.
- To elucidate the molecular mechanisms by which CD44 influences drug sensitivity.
Main Methods:
- CRISPR/Cas9 was used to knock down CD44 in osteosarcoma cells derived from Nf2-mutant mice.
- Doxorubicin sensitivity was assessed using immunoblot, colony formation, and WST-1 assays.
- RNA sequencing and qRT-PCR were employed to analyze gene expression changes.
Main Results:
- CD44 upregulates multidrug resistance (MDR) 1 protein, increasing resistance to doxorubicin.
- CD44 deletion activates p53 and increases Perp mRNA expression, impacting apoptosis.
- Proteolytic release of CD44 intracellular domain and hyaluronan interactions are suggested mechanisms.
Conclusions:
- CD44 is a key regulator of chemoresistance in osteosarcoma.
- Targeting CD44 could enhance the efficacy of standard chemotherapy for osteosarcoma patients.
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