Moores Cancer Center and.
Division of Biological Sciences, University of California San Diego, La Jolla, CA.
Blood. 2022 Jan 20;139(3):424-438. doi: 10.1182/blood.2020005693.
Posttranscriptional regulation has emerged as a driver for leukemia development and an avenue for therapeutic targeting. Among posttranscriptional processes, alternative polyadenylation (APA) is globally dysregulated across cancer types. However, limited studies have focused on the prevalence and role of APA in myeloid leukemia. Furthermore, it is poorly understood how altered poly(A) site usage of individual genes contributes to malignancy or whether targeting global APA patterns might alter oncogenic potential. In this study, we examined global APA dysregulation in patients with acute myeloid leukemia (AML) by performing 3' region extraction and deep sequencing (3'READS) on a subset of AML patient samples along with healthy hematopoietic stem and progenitor cells (HSPCs) and by analyzing publicly available data from a broad AML patient cohort. We show that patient cells exhibit global 3' untranslated region (UTR) shortening and coding sequence lengthening due to differences in poly(A) site (PAS) usage. Among APA regulators, expression of FIP1L1, one of the core cleavage and polyadenylation factors, correlated with the degree of APA dysregulation in our 3'READS data set. Targeting global APA by FIP1L1 knockdown reversed the global trends seen in patients. Importantly, FIP1L1 knockdown induced differentiation of t(8;21) cells by promoting 3'UTR lengthening and downregulation of the fusion oncoprotein AML1-ETO. In non-t(8;21) cells, FIP1L1 knockdown also promoted differentiation by attenuating mechanistic target of rapamycin complex 1 (mTORC1) signaling and reducing MYC protein levels. Our study provides mechanistic insights into the role of APA in AML pathogenesis and indicates that targeting global APA patterns can overcome the differentiation block in patients with AML.
转录后调控已成为白血病发生和治疗靶点的一个途径。在转录后过程中,可变多聚腺苷酸化(APA)在各种癌症类型中都存在广泛失调。然而,有限的研究集中在 APA 在髓系白血病中的普遍性和作用。此外,人们对个体基因的多聚腺苷酸化位点使用的改变如何促进恶性肿瘤形成,或者靶向全局 APA 模式是否会改变致癌潜能,知之甚少。在这项研究中,我们通过对一组急性髓系白血病(AML)患者样本进行 3' 区域提取和深度测序(3'READS),并分析来自广泛 AML 患者队列的公开数据,研究了 AML 患者中全局 APA 失调的情况。我们表明,由于多聚腺苷酸化位点(PAS)使用的差异,患者细胞表现出全局 3' 非翻译区(UTR)缩短和编码序列延长。在 APA 调节因子中,核心切割和多聚腺苷酸化因子之一 FIP1L1 的表达与我们的 3'READS 数据集中 APA 失调的程度相关。通过 FIP1L1 敲低靶向全局 APA 可逆转患者中观察到的全局趋势。重要的是,FIP1L1 敲低通过促进 3'UTR 延长和下调融合癌蛋白 AML1-ETO,诱导 t(8;21) 细胞分化。在非 t(8;21)细胞中,FIP1L1 敲低通过减弱雷帕霉素复合物 1(mTORC1)信号和降低 MYC 蛋白水平也促进分化。我们的研究提供了 APA 在 AML 发病机制中的作用的机制见解,并表明靶向全局 APA 模式可以克服 AML 患者的分化阻滞。