Division of Hematology, Department of Internal Medicine, College of Medicine, The Ohio State University, Columbus, OH.
Department of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH.
Blood. 2023 Sep 7;142(10):887-902. doi: 10.1182/blood.2022019419.
Mantle cell lymphoma (MCL) is an incurable B-cell malignancy with an overall poor prognosis, particularly for patients that progress on targeted therapies. Novel, more durable treatment options are needed for patients with MCL. Protein arginine methyltransferase 5 (PRMT5) is overexpressed in MCL and plays an important oncogenic role in this disease via epigenetic and posttranslational modification of cell cycle regulators, DNA repair genes, components of prosurvival pathways, and RNA splicing regulators. The mechanism of targeting PRMT5 in MCL remains incompletely characterized. Here, we report on the antitumor activity of PRMT5 inhibition in MCL using integrated transcriptomics of in vitro and in vivo models of MCL. Treatment with a selective small-molecule inhibitor of PRMT5, PRT-382, led to growth arrest and cell death and provided a therapeutic benefit in xenografts derived from patients with MCL. Transcriptional reprograming upon PRMT5 inhibition led to restored regulatory activity of the cell cycle (p-RB/E2F), apoptotic cell death (p53-dependent/p53-independent), and activation of negative regulators of B-cell receptor-PI3K/AKT signaling (PHLDA3, PTPROt, and PIK3IP1). We propose pharmacologic inhibition of PRMT5 for patients with relapsed/refractory MCL and identify MTAP/CDKN2A deletion and wild-type TP53 as biomarkers that predict a favorable response. Selective targeting of PRMT5 has significant activity in preclinical models of MCL and warrants further investigation in clinical trials.
套细胞淋巴瘤(MCL)是一种无法治愈的 B 细胞恶性肿瘤,总体预后较差,尤其是对于那些对靶向治疗进展的患者。MCL 患者需要新型、更持久的治疗选择。精氨酸甲基转移酶 5(PRMT5)在 MCL 中过度表达,通过细胞周期调节剂、DNA 修复基因、存活途径成分和 RNA 剪接调节剂的表观遗传和翻译后修饰,在该疾病中发挥重要致癌作用。PRMT5 在 MCL 中的靶向作用机制仍不完全清楚。在这里,我们报告了使用 MCL 的体外和体内模型的综合转录组学来研究 PRMT5 抑制在 MCL 中的抗肿瘤活性。用选择性的 PRMT5 小分子抑制剂 PRT-382 治疗导致生长停滞和细胞死亡,并为源自 MCL 患者的异种移植物提供了治疗益处。PRMT5 抑制后的转录重编程导致细胞周期(p-RB/E2F)、凋亡性细胞死亡(p53 依赖性/p53 非依赖性)和 B 细胞受体-PI3K/AKT 信号的负调节剂(PHLDA3、PTPROt 和 PIK3IP1)的调节活性恢复。我们建议对复发/难治性 MCL 患者进行 PRMT5 药物抑制,并确定 MTAP/CDKN2A 缺失和野生型 TP53 作为预测有利反应的生物标志物。PRMT5 的选择性靶向在 MCL 的临床前模型中具有显著活性,值得在临床试验中进一步研究。