Jin Yanli, Zhou Jingfeng, Xu Fang, Jin Bei, Cui Lijing, Wang Yun, Du Xin, Li Juan, Li Peng, Ren Ruibao, Pan Jingxuan
J Clin Invest. 2016 Oct 3;126(10):3961-3980. doi: 10.1172/JCI85239. Epub 2016 Sep 19.
Imatinib-insensitive leukemia stem cells (LSCs) are believed to be responsible for resistance to BCR-ABL tyrosine kinase inhibitors and relapse of chronic myelogenous leukemia (CML). Identifying therapeutic targets to eradicate CML LSCs may be a strategy to cure CML. In the present study, we discovered a positive feedback loop between BCR-ABL and protein arginine methyltransferase 5 (PRMT5) in CML cells. Overexpression of PRMT5 was observed in human CML LSCs. Silencing PRMT5 with shRNA or blocking PRMT5 methyltransferase activity with the small-molecule inhibitor PJ-68 reduced survival, serial replating capacity, and long-term culture-initiating cells (LTC-ICs) in LSCs from CML patients. Further, PRMT5 knockdown or PJ-68 treatment dramatically prolonged survival in a murine model of retroviral BCR-ABL-driven CML and impaired the in vivo self-renewal capacity of transplanted CML LSCs. PJ-68 also inhibited long-term engraftment of human CML CD34+ cells in immunodeficient mice. Moreover, inhibition of PRMT5 abrogated the Wnt/β-catenin pathway in CML CD34+ cells by depleting dishevelled homolog 3 (DVL3). This study suggests that epigenetic methylation modification on histone protein arginine residues is a regulatory mechanism to control self-renewal of LSCs and indicates that PRMT5 may represent a potential therapeutic target against LSCs.
伊马替尼不敏感的白血病干细胞(LSCs)被认为是慢性粒细胞白血病(CML)对BCR-ABL酪氨酸激酶抑制剂耐药及复发的原因。确定根除CML-LSCs的治疗靶点可能是治愈CML的一种策略。在本研究中,我们发现CML细胞中BCR-ABL与蛋白质精氨酸甲基转移酶5(PRMT5)之间存在正反馈回路。在人CML-LSCs中观察到PRMT5的过表达。用shRNA沉默PRMT5或用小分子抑制剂PJ-68阻断PRMT5甲基转移酶活性可降低CML患者LSCs的存活率、连续再植能力和长期培养起始细胞(LTC-ICs)。此外,PRMT5基因敲低或PJ-68处理显著延长了逆转录病毒BCR-ABL驱动的CML小鼠模型的生存期,并损害了移植的CML-LSCs的体内自我更新能力。PJ-68还抑制了免疫缺陷小鼠中人CML CD34+细胞的长期植入。此外,抑制PRMT5可通过消耗散乱同系物3(DVL3)消除CML CD34+细胞中的Wnt/β-连环蛋白通路。本研究表明,组蛋白精氨酸残基上的表观遗传甲基化修饰是控制LSCs自我更新的一种调节机制,并表明PRMT5可能是针对LSCs的潜在治疗靶点。