Robles Andrew J, Dai Wentao, Haldar Saikat, Ma Hongyan, Anderson Victoria M, Overacker Ross D, Risinger April L, Loesgen Sandra, Houghton Peter J, Cichewicz Robert H, Mooberry Susan L
Department of Pharmacology, The University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Mays Cancer Center, The University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Cancers (Basel). 2021 Dec 7;13(24):6176. doi: 10.3390/cancers13246176.
A screening program designed to identify natural products with selective cytotoxic effects against cell lines representing different types of pediatric solid tumors led to the identification of altertoxin II as a highly potent and selective cytotoxin against Ewing sarcoma cell lines. Altertoxin II, but not the related compounds altertoxin I and alteichin, was highly effective against every Ewing sarcoma cell line tested, with an average 25-fold selectivity for these cells as compared to cells representing other pediatric and adult cancers. Mechanism of action studies revealed that altertoxin II causes DNA double-strand breaks, a rapid DNA damage response, and cell cycle accumulation in the S phase. Our studies also demonstrate that the potent effects of altertoxin II are partially dependent on the progression through the cell cycle, because the G arrest initiated by a CDK4/6 inhibitor decreased antiproliferative potency more than 10 times. Importantly, the cell-type-selective DNA-damaging effects of altertoxin II in Ewing sarcoma cells occur independently of its ability to bind directly to DNA. Ultimately, we found that altertoxin II has a dose-dependent in vivo antitumor efficacy against a Ewing sarcoma xenograft, suggesting that it has potential as a therapeutic drug lead and will be useful to identify novel targets for Ewing-sarcoma-specific therapies.
一项旨在鉴定对代表不同类型小儿实体瘤的细胞系具有选择性细胞毒性作用的天然产物的筛选计划,导致鉴定出交替毒素II是一种针对尤因肉瘤细胞系的高效且选择性的细胞毒素。交替毒素II,而非相关化合物交替毒素I和交替菌素,对所测试的每个尤因肉瘤细胞系都非常有效,与代表其他小儿和成人癌症的细胞相比,对这些细胞的选择性平均高25倍。作用机制研究表明,交替毒素II会导致DNA双链断裂、快速的DNA损伤反应以及细胞周期在S期积累。我们的研究还表明,交替毒素II的强效作用部分取决于细胞周期进程,因为CDK4/6抑制剂引发的G期阻滞使抗增殖效力降低了10倍以上。重要的是,交替毒素II在尤因肉瘤细胞中对细胞类型有选择性的DNA损伤作用,与其直接结合DNA的能力无关。最终,我们发现交替毒素II对尤因肉瘤异种移植瘤具有剂量依赖性的体内抗肿瘤疗效,这表明它有作为治疗药物先导物的潜力,并且将有助于确定尤因肉瘤特异性治疗的新靶点。