发现端粒替代性延长(ALT)途径调节剂的一流高通量筛选方法

Merrill M. Froney, Christian R. Cook, Alyssa M. Cadiz, Katherine A. Flinter, Sara T. Ledeboer, Bianca Chan, Lauren E. Burris, Brian P. Hardy, Kenneth H. Pearce, Alexis C. Wardell, Brian T. Golitz, Michael B. Jarstfer, Samantha G. Pattenden
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摘要

端粒是防止染色体末端被识别为双链断裂的保护帽。在体细胞中,由于末端复制问题,端粒会随着每次细胞分裂而缩短,最终导致衰老,而衰老是为防止细胞失控生长而提出的检查点。肿瘤细胞通过激活两种端粒维持机制(TMM)之一来避免端粒缩短:端粒酶再激活或端粒替代性延长(ALT)。端粒维持机制在正常的分化细胞中并不活跃,因此是治疗癌症的可行靶点。目前有一种端粒酶抑制剂正在进行临床试验,但还没有已知的 ALT 抑制剂正在研发中,部分原因是人们对复杂的 ALT 途径还知之甚少。对于神经母细胞瘤和骨肉瘤等癌症来说,ALT 阳性与侵袭性表型和治疗选择少有关。因此,表征驱动 ALT 的关键生物通路的方法将提供重要的机理启示。我们已开发出一种首创的表型高通量筛选方法,用于鉴定 ALT 的小分子抑制剂。我们的筛选通过测量 ALT 特异性生物标志物相对 C-circle 水平来检测化合物治疗诱导的 ALT 活性变化。为了研究导致 ALT 的表观遗传机制,我们针对表观遗传靶向化合物库筛选了骨肉瘤和神经母细胞瘤细胞。命中的化合物包括靶向染色质调节蛋白和DNA损伤修复途径的化合物。总之,高通量 C-circle 检测将有助于扩大潜在 ALT 特异性治疗靶点的范围,并增加我们对 ALT 生物学的了解。
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A First-in-Class High-Throughput Screen to Discover Modulators of the Alternative Lengthening of Telomeres (ALT) Pathway
Telomeres are a protective cap that prevents chromosome ends from being recognized as double-stranded breaks. In somatic cells, telomeres shorten with each cell division due to the end replication problem, which eventually leads to senescence, a checkpoint proposed to prevent uncontrolled cell growth. Tumor cells avoid telomere shortening by activating one of two telomere maintenance mechanisms (TMMs): telomerase reactivation or alternative lengthening of telomeres (ALT). TMMs are a viable target for cancer treatment as they are not active in normal, differentiated cells. Whereas there is a telomerase inhibitor currently undergoing clinical trials, there are no known ALT inhibitors in development, partially because the complex ALT pathway is still poorly understood. For cancers such as neuroblastoma and osteosarcoma, the ALT-positive status is associated with an aggressive phenotype and few therapeutic options. Thus, methods that characterize the key biological pathways driving ALT will provide important mechanistic insight. We have developed a first-in-class phenotypic high-throughput screen to identify small-molecule inhibitors of ALT. Our screen measures relative C-circle level, an ALT-specific biomarker, to detect changes in ALT activity induced by compound treatment. To investigate epigenetic mechanisms that contribute to ALT, we screened osteosarcoma and neuroblastoma cells against an epigenetic-targeted compound library. Hits included compounds that target chromatin-regulating proteins and DNA damage repair pathways. Overall, the high-throughput C-circle assay will help expand the repertoire of potential ALT-specific therapeutic targets and increase our understanding of ALT biology.
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