Department of Experimental Therapeutics and.
Department of Leukemia, MD Anderson Cancer Center, The University of Texas, Houston, Texas, USA.
JCI Insight. 2020 Jan 16;5(1):121781. doi: 10.1172/jci.insight.121781.
Myelofibrosis (MF) is a myeloproliferative neoplasm characterized by cytopenia and extramedullary hematopoiesis, resulting in splenomegaly. Multiple pathological mechanisms (e.g., circulating cytokines and genetic alterations, such as JAKV617F mutation) have been implicated in the etiology of MF, but the molecular mechanism causing resistance to JAK2V617F inhibitor therapy remains unknown. Among MF patients who were treated with the JAK inhibitor ruxolitinib, we compared noncoding RNA profiles of ruxolitinib therapy responders versus nonresponders and found miR-543 was significantly upregulated in nonresponders. We validated these findings by reverse transcription-quantitative PCR. in this same cohort, in 2 additional independent MF patient cohorts from the United States and Romania, and in a JAK2V617F mouse model of MF. Both in vitro and in vivo models were used to determine the underlying molecular mechanism of miR-543 in MF. Here, we demonstrate that miR-543 targets the dioxygenases ten-eleven translocation 1 (TET1) and 2 (TET2) in patients and in vitro, causing increased levels of global 5-methylcytosine, while decreasing the acetylation of histone 3, STAT3, and tumor protein p53. Mechanistically, we found that activation of STAT3 by JAKs epigenetically controls miR-543 expression via binding the promoter region of miR-543. Furthermore, miR-543 upregulation promotes the expression of genes related to drug metabolism, including CYP3A4, which is involved in ruxolitinib metabolism. Our findings suggest miR-543 as a potentially novel biomarker for the prognosis of MF patients with a high risk of treatment resistance and as a potentially new target for the development of new treatment options.
骨髓纤维化(MF)是一种骨髓增生性肿瘤,其特征为细胞减少症和骨髓外造血,导致脾肿大。多种病理机制(例如,循环细胞因子和基因改变,如 JAKV617F 突变)与 MF 的病因有关,但导致对 JAK2V617F 抑制剂治疗耐药的分子机制尚不清楚。在接受 JAK 抑制剂芦可替尼治疗的 MF 患者中,我们比较了芦可替尼治疗应答者与无应答者的非编码 RNA 谱,发现 miR-543 在无应答者中显著上调。我们通过逆转录定量 PCR 验证了这些发现。在同一队列中,我们还在来自美国和罗马尼亚的另外 2 个独立的 MF 患者队列以及 MF 的 JAK2V617F 小鼠模型中验证了这些发现。我们使用体外和体内模型来确定 miR-543 在 MF 中的潜在分子机制。在这里,我们证明 miR-543 在患者和体外靶向双加氧酶 ten-eleven 易位 1(TET1)和 2(TET2),导致全基因组 5-甲基胞嘧啶水平升高,同时降低组蛋白 3、STAT3 和肿瘤蛋白 p53 的乙酰化。从机制上讲,我们发现 JAKs 通过 STAT3 的激活通过结合 miR-543 启动子区域来表观遗传控制 miR-543 的表达。此外,miR-543 的上调促进与药物代谢相关的基因的表达,包括 CYP3A4,其参与芦可替尼的代谢。我们的研究结果表明 miR-543 可作为预后标志物,用于预测 MF 患者发生治疗耐药的风险,并可能成为开发新治疗选择的新靶点。