A high-throughput screening identifies MCM chromatin loading inhibitors targeting cells with increased replication origins

被引:0
|
作者
Falbo, Lucia [1 ,2 ]
Techer, Herve [1 ,6 ]
Sannino, Vincenzo [1 ]
Robusto, Michela [1 ]
Faga, Giovanni [1 ,4 ]
Pezzimenti, Federica [1 ]
Romeo, Francesco [1 ,2 ]
Colombo, Luca Gabriele [1 ]
Vultaggio, Stefania [1 ,5 ]
Fancelli, Daniele [1 ]
Monzani, Silvia [3 ]
Cecatiello, Valentina [3 ,4 ]
Pasqualato, Sebastiano [3 ,4 ]
Varasi, Mario [1 ]
Mercurio, Ciro [1 ]
Costanzo, Vincenzo [1 ,2 ]
机构
[1] AIRC Inst Mol Oncol, IFOM ETS, Milan, Italy
[2] Univ Milan, Dept Oncol & Hematol Oncol, I-20133 Milan, Italy
[3] European Inst Oncol IEO IRCCS, Dept Expt Oncol, I-20141 Milan, Italy
[4] Human Technopole, Viale Rita,Levi Montalcini 1, I-20157 Milan, Italy
[5] ICON PLC, via Benigno Crespi 19, I-20159 Milan, Italy
[6] Univ Cote Azur, Inst Res Canc & Aging Nice IRCAN, CNRS, INSERM, Nice, France
基金
欧洲研究理事会;
关键词
DNA-DAMAGE RESPONSE; DORMANT ORIGINS; EXCESS MCM2-7; PROTEINS; GEMININ; COMPLEX; POTENT; CDC6; OVEREXPRESSION; MARKER;
D O I
10.1016/j.isci.2024.110567
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 Xenopus laevis 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 Xenopus 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.
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页数:24
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