Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Portland, OR, USA; Department of Pharmaceutics, College of Pharmacy, Jazan University, Jazan, Saudi Arabia.
Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Portland, OR, USA.
Nanomedicine. 2021 Oct;37:102446. doi: 10.1016/j.nano.2021.102446. Epub 2021 Jul 23.
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.
尤因氏肉瘤(EwS)是儿童和青少年中第二常见的骨癌。目前的化疗方案在复发性疾病患者中主要无效,并在幸存者中造成长期影响。因此,我们基于一种名为 ML111 的新型药物候选物开发了一种联合治疗方法,该药物对 EwS 细胞具有选择性活性,并与长春新碱协同作用。为了提高疏水性 ML111 的水溶解度,开发了聚合物纳米颗粒(ML111-NP)。体外数据显示,ML111-NP 不会影响非恶性细胞,但其会降低 EwS 细胞的活力。此外,ML111-NP 与长春新碱联合对 EwS 细胞具有强烈的协同作用,而这对药物组合对正常细胞表现出拮抗作用。最后,动物研究证实,静脉注射 ML111-NP 后可有效在原位 EwS 异种移植瘤中积累,并与长春新碱联合使用可提供更好的治疗效果,而无明显毒性。这些结果支持基于 ML111 的联合治疗方法在 EwS 中的潜力。