Experimental and Clinical Research Center (ECRC) of the MDC and Charité Berlin, Berlin, Germany.
Department of Pediatric Oncology and Hematology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin, Germany.
Nat Commun. 2022 Jul 25;13(1):4297. doi: 10.1038/s41467-022-32023-7.
Despite advances in multi-modal treatment approaches, clinical outcomes of patients suffering from PAX3-FOXO1 fusion oncogene-expressing alveolar rhabdomyosarcoma (ARMS) remain dismal. Here we show that PAX3-FOXO1-expressing ARMS cells are sensitive to pharmacological ataxia telangiectasia and Rad3 related protein (ATR) inhibition. Expression of PAX3-FOXO1 in muscle progenitor cells is not only sufficient to increase sensitivity to ATR inhibition, but PAX3-FOXO1-expressing rhabdomyosarcoma cells also exhibit increased sensitivity to structurally diverse inhibitors of ATR. Mechanistically, ATR inhibition leads to replication stress exacerbation, decreased BRCA1 phosphorylation and reduced homologous recombination-mediated DNA repair pathway activity. Consequently, ATR inhibitor treatment increases sensitivity of ARMS cells to PARP1 inhibition in vitro, and combined treatment with ATR and PARP1 inhibitors induces complete regression of primary patient-derived ARMS xenografts in vivo. Lastly, a genome-wide CRISPR activation screen (CRISPRa) in combination with transcriptional analyses of ATR inhibitor resistant ARMS cells identifies the RAS-MAPK pathway and its targets, the FOS gene family, as inducers of resistance to ATR inhibition. Our findings provide a rationale for upcoming biomarker-driven clinical trials of ATR inhibitors in patients suffering from ARMS.
尽管多模式治疗方法取得了进展,但患有 PAX3-FOXO1 融合基因表达肺泡横纹肌肉瘤 (ARMS) 的患者的临床结局仍然不佳。在这里,我们表明表达 PAX3-FOXO1 的 ARMS 细胞对药理学共济失调毛细血管扩张症和 Rad3 相关蛋白 (ATR) 抑制敏感。PAX3-FOXO1 在肌肉祖细胞中的表达不仅足以增加对 ATR 抑制的敏感性,而且表达 PAX3-FOXO1 的横纹肌肉瘤细胞对结构不同的 ATR 抑制剂也表现出更高的敏感性。从机制上讲,ATR 抑制导致复制应激加剧、BRCA1 磷酸化减少和同源重组介导的 DNA 修复途径活性降低。因此,ATR 抑制剂治疗可增加 ARMS 细胞在体外对 PARP1 抑制的敏感性,ATR 和 PARP1 抑制剂联合治疗可诱导体内原发性患者来源的 ARMS 异种移植物的完全消退。最后,ATR 抑制剂耐药 ARMS 细胞的全基因组 CRISPR 激活筛选 (CRISPRa) 结合转录分析确定 RAS-MAPK 途径及其靶标 FOS 基因家族是对 ATR 抑制产生抗性的诱导剂。我们的研究结果为即将进行的 ATR 抑制剂在 ARMS 患者中的生物标志物驱动的临床试验提供了依据。