Aslan Derya, Garde Christian, Nygaard Mette Katrine, Helbo Alexandra Søgaard, Dimopoulos Konstantinos, Hansen Jakob Werner, Severinsen Marianne Tang, Treppendahl Marianne Bach, Sjø Lene Dissing, Grønbæk Kirsten, Kristensen Lasse Sommer
Department of Hematology, Rigshospitalet, Copenhagen, Denmark.
Center for Biological Sequence Analysis, Department of Systems Biology, Technical University of Denmark, Kgs. Lyngby, Denmark.
Oncotarget. 2016 Mar 1;7(9):9951-63. doi: 10.18632/oncotarget.7127.
Spliceosome mutations are frequently observed in patients with myelodysplastic syndromes (MDS). However, it is largely unknown how these mutations contribute to the disease. MicroRNAs (miRNAs) are small noncoding RNAs, which have been implicated in most human cancers due to their role in post transcriptional gene regulation. The aim of this study was to analyze the impact of spliceosome mutations on the expression of miRNAs in a cohort of 34 MDS patients. In total, the expression of 76 miRNAs, including mirtrons and splice site overlapping miRNAs, was accurately quantified using reverse transcriptase quantitative PCR. The majority of the studied miRNAs have previously been implicated in MDS. Stably expressed miRNA genes for normalization of the data were identified using GeNorm and NormFinder algorithms. High-resolution melting assays covering all mutational hotspots within SF3B1, SRSF2, and U2AF1 (U2AF35) were developed, and all detected mutations were confirmed by Sanger sequencing. Overall, canonical miRNAs were downregulated in spliceosome mutated samples compared to wild-type (P = 0.002), and samples from spliceosome mutated patients clustered together in hierarchical cluster analyses. Among the most downregulated miRNAs were several tumor-suppressor miRNAs, including several let-7 family members, miR-423, and miR-103a. Finally, we observed that the predicted targets of the most downregulated miRNAs were involved in apoptosis, hematopoiesis, and acute myeloid leukemia among other cancer- and metabolic pathways. Our data indicate that spliceosome mutations may play an important role in MDS pathophysiology by affecting the expression of tumor suppressor miRNA genes involved in the development and progression of MDS.
剪接体突变在骨髓增生异常综合征(MDS)患者中经常被观察到。然而,这些突变如何导致该疾病在很大程度上尚不清楚。微小RNA(miRNA)是小的非编码RNA,由于其在转录后基因调控中的作用,已被认为与大多数人类癌症有关。本研究的目的是分析34例MDS患者队列中剪接体突变对miRNA表达的影响。使用逆转录定量PCR准确地定量了总共76种miRNA的表达,包括mirtrons和剪接位点重叠的miRNA。大多数研究的miRNA以前已被认为与MDS有关。使用GeNorm和NormFinder算法鉴定了用于数据标准化的稳定表达的miRNA基因。开发了覆盖SF3B1、SRSF2和U2AF1(U2AF35)内所有突变热点的高分辨率熔解分析,并且所有检测到的突变均通过桑格测序得到证实。总体而言,与野生型相比,剪接体突变样本中的典型miRNA下调(P = 0.002),并且来自剪接体突变患者的样本在层次聚类分析中聚集在一起。下调最明显的miRNA中有几种肿瘤抑制性miRNA,包括几种let-7家族成员、miR-423和miR-103a。最后,我们观察到下调最明显的miRNA的预测靶标参与细胞凋亡、造血和急性髓细胞白血病以及其他癌症和代谢途径。我们的数据表明,剪接体突变可能通过影响参与MDS发生和发展的肿瘤抑制性miRNA基因的表达,在MDS病理生理学中发挥重要作用。