Combination drug screen identifies synergistic drug interaction of BCL-XL and class I histone deacetylase inhibitors in MYC-amplified medulloblastoma cells

被引:5
|
作者
Zeuner, Simon [1 ,2 ,3 ]
Vollmer, Johanna [1 ,2 ,3 ]
Sigaud, Romain [1 ,2 ,3 ]
Oppermann, Sina [1 ,2 ,3 ]
Peterziel, Heike [1 ,2 ,3 ]
Elharouni, Dina [5 ]
Oehme, Ina [1 ,2 ,3 ]
Witt, Olaf [1 ,2 ,3 ,4 ]
Milde, Till [1 ,2 ,3 ,4 ]
Ecker, Jonas [1 ,2 ,3 ,4 ]
机构
[1] Hopp Childrens Canc Ctr Heidelberg KiTZ, Neuenheimer Feld 430, D-69120 Heidelberg, Germany
[2] Heidelberg Univ Hosp, Natl Ctr Tumor Dis NCT, NCT Heidelberg DKFZ, Neuenheimer Feld 460, D-69120 Heidelberg, Germany
[3] German Consortium Translat Canc Res DKTK, German Canc Res Ctr DKFZ, Clin Cooperat Unit Pediat Oncol, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
[4] Heidelberg Univ Hosp, Dept Pediat Hematol & Oncol, Neuenheimer Feld 430, D-69120 Heidelberg, Germany
[5] German Canc Res Ctr, Dept Bioinformat & Om Data Analyt, Heidelberg, Germany
关键词
Drug screen; Medulloblastoma; MYC; HDAC; BCL-XL; INDUCED APOPTOSIS; HETEROGENEITY; CHEMOTHERAPY; HDAC;
D O I
10.1007/s11060-023-04526-w
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposePatients with MYC-amplified Group 3 medulloblastoma (MB) (subtype II) show poor progression-free survival rates. Class I histone deacetylase inhibitors (HDACi) are highly effective for the treatment of MYC-amplified MB in vitro and in vivo. Drug combination regimens including class I HDACi may represent an urgently needed novel treatment approach for this high risk disease.MethodsA medium-throughput in vitro combination drug screen was performed in three MYC-amplified and one non-MYC-amplified MB cell line testing 75 clinically relevant drugs alone and in combination with entinostat. The drug sensitivity score (DSS) was calculated based on metabolic inhibition quantified by CellTiter-Glo. The six top synergistic combination hits were evaluated in a 5 x 5 combination matrix and a seven-ray design. Synergy was validated and characterized by cell counts, caspase-3-like-activity and poly-(ADP-ribose)-polymerase-(PARP)-cleavage. On-target activity of drugs was validated by immunoprecipitation and western blot. BCL-XL dependency of the observed effect was explored with siRNA mediated knockdown of BCL2L1, and selective inhibition with targeted compounds (A-1331852, A-1155463).Results20/75 drugs effectively reduced metabolic activity in combination with entinostat in all three MYC-amplified cell lines (DSS >= 10). The combination entinostat and navitoclax showed the strongest synergistic interaction across all MYC-amplified cell lines. siRNA mediated knockdown of BCL2L1, as well as targeted inhibition with selective inhibitors showed BCL-XL dependency of the observed effect. Increased cell death was associated with increased caspase-3-like-activity.ConclusionOur study identifies the combination of class I HDACi and BCL-XL inhibitors as a potential new approach for the treatment of MYC-amplified MB cells.Graphical abstractGraphical abstract created with BioRender.com, illustrating the workflow and summarizing main results.{GRAPHIACAL ABSTRACT}
引用
收藏
页码:99 / 112
页数:14
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