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ONC201 治疗促结缔组织增生性小圆细胞肿瘤的疗效。

Efficacy of ONC201 in Desmoplastic Small Round Cell Tumor.

机构信息

Division of Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit, 1484, Houston, TX, USA.

Division of Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit, 1484, Houston, TX, USA.

出版信息

Neoplasia. 2018 May;20(5):524-532. doi: 10.1016/j.neo.2018.02.006. Epub 2018 Apr 5.

Abstract

Desmoplastic Small Round Cell Tumor (DSRCT) is a rare sarcoma tumor of adolescence and young adulthood, which harbors a recurrent chromosomal translocation between the Ewing's sarcoma gene (EWSR1) and the Wilms' tumor suppressor gene (WT1). Patients usually develop multiple abdominal tumors with liver and lymph node metastasis developing later. Survival is poor using a multimodal therapy that includes chemotherapy, radiation and surgical resection, new therapies are needed for better management of DSRCT. Triggering cell apoptosis is the scientific rationale of many cancer therapies. Here, we characterized for the first time the expression of pro-apoptotic receptors, tumor necrosis-related apoptosis-inducing ligand receptors (TRAILR1-4) within an established human DSRCT cell line and clinical samples. The molecular induction of TRAIL-mediated apoptosis using agonistic small molecule, ONC201 in vitro cell-based proliferation assay and in vivo novel orthotopic xenograft animal models of DSRCT, was able to inhibit cell proliferation that was associated with caspase activation, and tumor growth, indicating that a cell-based delivery of an apoptosis-inducing factor could be relevant therapeutic agent to control DSRCT.

摘要

促凋亡型小细胞圆形细胞瘤(DSRCT)是一种罕见的青少年和青年期肉瘤肿瘤,其具有 Ewing 肉瘤基因(EWSR1)和 Wilms 肿瘤抑制基因(WT1)之间的反复染色体易位。患者通常会发展出多个腹部肿瘤,并伴有肝和淋巴结转移。采用化疗、放疗和手术切除的多模式治疗,生存情况较差,需要新的治疗方法来更好地管理 DSRCT。触发细胞凋亡是许多癌症治疗的科学依据。在这里,我们首次对建立的人 DSRCT 细胞系和临床样本中促凋亡受体、肿瘤坏死相关凋亡诱导配体受体(TRAILR1-4)的表达进行了特征描述。在体外细胞增殖测定和新的 DSRCT 原位异种移植动物模型中,使用激动性小分子 ONC201 诱导 TRAIL 介导的细胞凋亡,能够抑制与半胱天冬酶激活和肿瘤生长相关的细胞增殖,表明细胞凋亡诱导因子的基于细胞的递呈可能是控制 DSRCT 的相关治疗剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3901/5915995/6b4251635a64/gr1.jpg

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