首页> 外文期刊>Acta Haematologica >MicroRNA expression and JAK2 allele burden in bone marrow trephine biopsies of polycythemia vera, essential thrombocythemia and early primary myelofibrosis
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MicroRNA expression and JAK2 allele burden in bone marrow trephine biopsies of polycythemia vera, essential thrombocythemia and early primary myelofibrosis

机译:真性红细胞增多症,原发性血小板增多症和早期原发性骨髓纤维化的骨髓冰毒活检中MicroRNA表达和JAK2等位基因负担

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Background/Aims: MicroRNAs (miRNAs) play an important role in cellular differentiation and cancer pathogenesis. However, their role in promoting the malignant phenotype of myeloproliferative diseases and their importance for differential diagnosis of early-stage chronic myeloproliferative diseases (CMPDs) remains widely obscure. Methods: In this study, we systematically evaluated the differential expression of miRNAs previously described to be associated with myelopoiesis and myeloproliferative pathogenesis by quantitative RT-PCR in polycythemia vera, essential thrombocythemia, early primary myelofibrosis (PMF) and normal hematopoiesis. Our goal was to establish certain miRNAs as potential markers for CMPDs to facilitate the differentiation between these diseases and to further investigate molecular differences between the subtypes of myeloproliferative neoplasia. Results: An aberrant expression of miRNAs 10a and 150 could be demonstrated for essential thrombocythemia and PMF as well as for polycythemia vera and PMF, respectively. The expression of miR-150 could further be shown to correlate with both JAK2 allele burden and peripheral blood counts. Conclusion: Thus, the miRNAs investigated in this study seem to be potential marker oncomiRs in the differential diagnosis of CMPDs and possibly hold potential for the elucidation of a JAK2-independent mechanism of pathogenesis.
机译:背景/目的:MicroRNA(miRNA)在细胞分化和癌症发病机理中起重要作用。然而,它们在促进骨髓增生性疾病的恶性表型中的作用及其对早期慢性骨髓增生性疾病(CMPDs)的鉴别诊断的重要性仍然广为人知。方法:在这项研究中,我们通过定量RT-PCR系统评价了先前描述的与骨髓造血和骨髓增生病发病机制相关的miRNA的差异表达,包括真性红细胞增多症,原发性血小板增多症,早期原发性骨髓纤维化(PMF)和正常造血。我们的目标是建立某些miRNAs作为CMPD的潜在标志物,以促进这些疾病之间的分化,并进一步研究骨髓增生性瘤形成亚型之间的分子差异。结果:原发性血小板增多症和PMF以及真性红细胞增多症和原发性红细胞增多症的miRNA 10a和150分别表达异常。 miR-150的表达可进一步显示与JAK2等位基因负荷和外周血细胞计数相关。结论:因此,本研究中研究的miRNA似乎是CMPD鉴别诊断中潜在的oncomiRs标记,可能具有阐明与JAK2无关的发病机理的潜力。

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