Zhou Min, Huang Yi, Xu Ping, Li Shuyi, Duan Chen, Lin Xiaoying, Bao Shilai, Zou Waiyi, Pan Jingxuan, Liu Chang, Jin Yanli
State Key Laboratory of Bioactive Molecules and Druggability Assessment, Jinan University, Guangzhou, 510632, China.
Jinan University Institute of Tumor Pharmacology, College of Pharmacy, Jinan University, Guangzhou, 510632, China.
Adv Sci (Weinh). 2025 Feb;12(5):e2308586. doi: 10.1002/advs.202308586. Epub 2024 Dec 12.
The application of tyrosine kinase inhibitors (TKIs) has revolutionized the management of chronic myeloid leukemia (CML). However, disease relapse and progression particularly due to persistent leukemia stem cells (LSCs) remain a big challenge in the clinic. Therefore, validation of the therapeutic vulnerability in LSCs is urgently needed. This study verifies the critical role of protein arginine methyltransferase 1 (PRMT1) in the maintenance of CML LSCs. It is found that PRMT1 promotes the survival and serially plating abilities of human primary CML LSCs. Genetic deletion of Prmt1 significantly delays the leukemogenesis and impairs the self-renewal of LSCs in BCR-ABL-driven CML mice. PRMT1 regulates LSCs and leukemia development depending on its methyltransferase activity. Pharmacological inhibition of PRMT1 activity by MS023 remarkably eliminates LSCs and prolongs the survival of CML mice. Mechanistical studies reveal that PRMT1 promotes transcriptional activation of ribosomal protein L29 (RPL29) via catalyzing asymmetric dimethylation of histone H4R3 (H4R3me2a) at its gene promoter region. PRMT1 augments the global protein synthesis via RPL29 in CML LSCs. Taken together, the findings provide new evidence that histone arginine methylation modification regulates protein synthesis in LSCs and highlight PRMT1 as a valuable druggable target for patients with CML.
酪氨酸激酶抑制剂(TKIs)的应用彻底改变了慢性粒细胞白血病(CML)的治疗方式。然而,疾病复发和进展,尤其是由于持续性白血病干细胞(LSCs)导致的复发和进展,仍然是临床上的一大挑战。因此,迫切需要验证LSCs中的治疗易损性。本研究验证了蛋白质精氨酸甲基转移酶1(PRMT1)在维持CML LSCs中的关键作用。研究发现,PRMT1可促进人原发性CML LSCs的存活和连续传代能力。在BCR-ABL驱动的CML小鼠中,Prmt1基因缺失显著延迟白血病发生并损害LSCs的自我更新能力。PRMT1依赖其甲基转移酶活性调节LSCs和白血病发展。MS023对PRMT1活性的药理抑制作用可显著消除LSCs并延长CML小鼠的生存期。机制研究表明,PRMT1通过催化核糖体蛋白L29(RPL29)基因启动子区域组蛋白H4R3(H4R3me2a)的不对称二甲基化来促进其转录激活。PRMT1通过RPL29增强CML LSCs中的整体蛋白质合成。综上所述,这些发现提供了新的证据,表明组蛋白精氨酸甲基化修饰调节LSCs中的蛋白质合成,并突出了PRMT1作为CML患者有价值的可药物靶向。