Falbo Lucia, Técher Hervé, Sannino Vincenzo, Robusto Michela, Fagà Giovanni, Pezzimenti Federica, Romeo Francesco, Colombo Luca Gabriele, Vultaggio Stefania, Fancelli Daniele, Monzani Silvia, Cecatiello Valentina, Pasqualato Sebastiano, Varasi Mario, Mercurio Ciro, Costanzo Vincenzo
IFOM-ETS, The AIRC Institute of Molecular Oncology, Milan, Italy.
Department of Oncology and Hematology-Oncology, University of Milan, 20133 Milan, Italy.
iScience. 2024 Jul 22;27(8):110567. doi: 10.1016/j.isci.2024.110567. eCollection 2024 Aug 16.
Replication origin assembly is a pivotal step in chromosomal DNA replication. In this process, the ORC complex binds DNA and, together with the CDC6 and CDT1, promotes the loading of the MCM helicase. Chemicals targeting origin assembly might be useful to sensitize highly proliferative cancer cells. However, identifying such compounds is challenging due to the multistage nature of this process. Here, using egg extract we set up a high-throughput screening to isolate MCM chromatin loading inhibitors, which led to the identification of NSC-95397 as a powerful inhibitor of replication origin assembly that targets CDC6 protein and promotes its degradation. Using systems developed to test selective drug-induced lethality we show that NSC-95397 triggers cell death both in human cells and embryos that have higher proliferative ability. These findings demonstrate the effectiveness of molecules disrupting DNA replication processes in targeting hyperproliferating cells, highlighting their potential as anti-cancer molecules.
复制起点组装是染色体DNA复制中的关键步骤。在此过程中,ORC复合物结合DNA,并与CDC6和CDT1一起促进MCM解旋酶的加载。靶向起点组装的化学物质可能有助于使高度增殖的癌细胞敏感化。然而,由于这个过程的多阶段性质,鉴定此类化合物具有挑战性。在这里,我们使用卵提取物建立了高通量筛选以分离MCM染色质加载抑制剂,这导致鉴定出NSC-95397是一种强大的复制起点组装抑制剂,它靶向CDC6蛋白并促进其降解。使用开发用于测试选择性药物诱导的致死性的系统,我们表明NSC-95397在具有较高增殖能力的人类细胞和胚胎中均触发细胞死亡。这些发现证明了破坏DNA复制过程的分子在靶向过度增殖细胞方面的有效性,突出了它们作为抗癌分子的潜力。