| Literature DB >> 34303840 |
Fahad Y Sabei1, Olena Taratula2, Hassan A Albarqi3, Adel M Al-Fatease4, Abraham S Moses2, Ananiya A Demessie2, Youngrong Park2, Walter K Vogel2, Ellie Esfandiari Nazzaro2, Monika A Davare5, Adam Alani2, Mark Leid6, Oleh Taratula7.
Abstract
Ewing's sarcoma (EwS) is the second most common bone cancer in children and adolescents. Current chemotherapy regimens are mainly ineffective in patients with relapsed disease and cause long-term effects in survivors. Therefore, we have developed a combinatorial therapy based on a novel drug candidate named ML111 that exhibits selective activity against EwS cells and synergizes with vincristine. To increase the aqueous solubility of hydrophobic ML111, polymeric nanoparticles (ML111-NP) were developed. In vitro data revealed that ML111-NP compromise viability of EwS cells without affecting non-malignant cells. Furthermore, ML111-NP exhibit strong synergistic effects in a combination with vincristine on EwS cells, while this drug pair exhibits antagonistic effects towards normal cells. Finally, animal studies validated that ML111-NP efficiently accumulate in orthotopic EwS xenografts after intravenous injection and provide superior therapeutic outcomes in a combination with vincristine without evident toxicity. These results support the potential of the ML111-based combinatorial therapy for EwS.Entities:
Keywords: Chemotherapy; Combinatorial therapy; Ewing's sarcoma; ML111; Nanoparticle
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Year: 2021 PMID: 34303840 PMCID: PMC8464505 DOI: 10.1016/j.nano.2021.102446
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 6.096