Repurposing Romidepsin for Osteosarcoma: Screening FDA-Approved Oncology Drugs with Three-Dimensional Osteosarcoma Spheroids.

Emily E Seiden, Spencer M Richardson, Leah A Everitt, Gabrielle J Knafler, Gavin P Kinsella, Alyssa L Walker, Venetia A Whiteside, James D Buschbach, Deep A Gandhi, M Reza Saadatzadeh, L Daniel Wurtz, Patrick J Getty, Sheldon L Padgett, Rance M Gamblin, Michael O Childress, Christopher M Fulkerson, Karen E Pollok, Christopher D Collier, Edward M Greenfield
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Abstract

Osteosarcoma is the most common primary malignant bone tumor and predominantly affects children, adolescents, and young adults. It is the third most common cause of cancer-related deaths among 9-24-year-olds. Despite aggressive chemotherapeutic and surgical therapies, the survival rate is only 25% for patients with detectable lung metastases at diagnosis and only 70% in patients that present without detectable lung metastases. The poor prognosis is due to growth of metastases irrespective of whether they are initially large enough to detect clinically. It is therefore necessary to develop new methods to target the growth of lung micrometastases. An NCI panel of FDA-approved oncology drugs was therefore screened using three highly metastatic human osteosarcoma cell lines. To more closely approximate in vivo micro-metastases, the screen used a 3D multicellular in vitro osteosarcoma spheroid (sarcosphere) model. Among 13 hits from the initial screen, we identified the histone deacetylase inhibitor (HDI) romidepsin as the most promising inhibitor in secondary screens based on sarcosphere viability. Romidepsin potency was evident with and without standard-of-care chemotherapeutics (MAP: Methotrexate, Adriamycin, Cisplatin) at drug concentrations that are clinically achievable and did not affect non-transformed cells. By those criteria, romidepsin also substantially outperformed the other three FDA-approved HDIs and eight HDIs in clinical trials. Importantly, sarcospheres derived from 30-50% of human and canine patient samples were also sensitive to romidepsin with ED50s 10- to 700-fold less than the Cmax in human patients. Based on these 3-D screening approaches, romidepsin is a promising drug to repurpose for osteosarcoma.

Significance statement: Our unbiased sarcosphere-based drug screen identified romidepsin as a promising candidate to repurpose for canine and human patients with metastatic osteosarcoma. This screening strategy allowed us to identify romidepsin-sensitive and -resistant patients. Sarcosphere-based screening may therefore be useful to stratify patients most likely to respond clinically to romidepsin or other drugs.

罗米地辛对骨肉瘤的再利用:fda批准的三维类骨肉瘤肿瘤药物的筛选
骨肉瘤是最常见的原发性恶性骨肿瘤,主要影响儿童、青少年和年轻人。它是9-24岁人群中癌症相关死亡的第三大常见原因。尽管进行了积极的化疗和手术治疗,但诊断时可检测到肺转移的患者的生存率仅为25%,而未检测到肺转移的患者的生存率仅为70%。预后不良是由于转移瘤的生长,无论它们最初是否大到足以在临床上发现。因此,有必要开发新的方法来靶向肺微转移瘤的生长。因此,使用三种高度转移的人骨肉瘤细胞系筛选了一组经fda批准的NCI肿瘤药物。为了更接近体内微转移,筛选使用3D多细胞体外骨肉瘤球形(肌球)模型。在最初筛选的13个hit中,基于肌球活力,我们确定组蛋白去乙酰化酶抑制剂(HDI)罗米地辛是二次筛选中最有希望的抑制剂。无论是否使用标准化疗药物(MAP:甲氨蝶呤、阿霉素、顺铂),在临床可达到的药物浓度下,罗米地辛的效力都是明显的,并且不影响非转化细胞。根据这些标准,罗米地辛在临床试验中也大大优于其他三种fda批准的hdi和八种hdi。重要的是,来自30-50%的人类和犬患者样本的肌球也对罗米地辛敏感,其ed50比人类患者的Cmax低10- 700倍。基于这些三维筛选方法,罗米地辛是一种很有希望用于骨肉瘤的药物。意义声明:我们无偏倚的基于肌球的药物筛选确定罗米地辛是一种有希望用于犬和人类转移性骨肉瘤患者的候选药物。这种筛选策略使我们能够识别对罗米地辛敏感和耐药的患者。因此,基于肌球的筛查可能有助于对最有可能对罗米地辛或其他药物有临床反应的患者进行分层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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