造血干细胞移植后急性髓系白血病患者MiR-19b、MiR-25、MiR-17、WT1和CEBPA表达异常与移植物抗宿主病的关系

IF 0.6 Q4 ONCOLOGY
Mahdiyar Iravani Saadi, Fatemeh Tahmasebijaroubi, Esmat Noshadi, Raha Rahimikian, Zahed Karimi, Maryam Owjfard, Ahmad Niknam, Ehsan Nabi Abdolyousefi, Sanaz Salek, Reza Tabrizi, Elham Jamali
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引用次数: 0

摘要

急性髓性白血病(AML)是一种血液恶性肿瘤,其特征是骨髓和血液中异常细胞的增殖干扰正常血细胞。我们研究了微核糖核酸(miR)-19b、miR-17和miR-25、Wilms肿瘤(WT1)和CCAAT增强子结合蛋白α (CEBPA)基因表达水平的变化是否影响AML患者的疾病预后和临床结果。材料和方法采用定量SYBR Green实时聚合酶链反应方法,评估miR-19-b、miR-17和miR-25以及WT1和CEBPA基因在一组患者和对照组以及不同风险组(高、中、低风险)、M3与非M3、移植物抗宿主病(GvHD)与非GvHD患者中的表达水平。结果与化疗前诊断时的基线水平相比,化疗后AML患者miR-19b和miR-17的表达明显升高。AML患者M3亚组和非M3亚组中miR-19b和miR-25的表达水平差异显著。MiR-19b和miR-25在GvHD患者中表达升高,而MiR-19b和miR-25在GvHD患者中与非GvHD患者相比表达有所降低,但差异无统计学意义。此外,不同细胞遗传畸变的患者miR-19-b和miR-25表达水平相似。结论MiR-19b、miR-17、miR-25在AML患者外周血白细胞中表达异常,可能在造血干细胞移植后急性GvHD的发生发展中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dysregulated Expression of MiR-19b, MiR-25, MiR-17, WT1, and CEBPA in Patients with Acute Myeloid Leukemia and Association with Graft versus Host Disease after Hematopoietic Stem Cell Transplantation.

Dysregulated Expression of MiR-19b, MiR-25, MiR-17, WT1, and CEBPA in Patients with Acute Myeloid Leukemia and Association with Graft versus Host Disease after Hematopoietic Stem Cell Transplantation.

Dysregulated Expression of MiR-19b, MiR-25, MiR-17, WT1, and CEBPA in Patients with Acute Myeloid Leukemia and Association with Graft versus Host Disease after Hematopoietic Stem Cell Transplantation.

Dysregulated Expression of MiR-19b, MiR-25, MiR-17, WT1, and CEBPA in Patients with Acute Myeloid Leukemia and Association with Graft versus Host Disease after Hematopoietic Stem Cell Transplantation.

Elham JamaliObjectives  Acute myeloid leukemia (AML) is a blood malignancy characterized by the proliferation of aberrant cells in the bone marrow and blood that interfere with normal blood cells. We have investigated whether changes in the level of micro-ribonucleic acid (miR)-19b, miR-17, and miR-25, Wilms' tumor (WT1), and CCAAT enhancer-binding protein α (CEBPA) genes expression affect disease prognosis and clinical outcome in AML patients. Materials and Methods  The expression level of miR-19-b, miR-17, and miR-25, as well as WT1 and CEBPA genes in a group of patients and controls as well as different risk groups (high, intermediate, and favorite risk), M3 versus non-M3, and graft-versus-host disease (GvHD) versus non-GvHD patients were assessed using a quantitative SYBR Green real-time polymerase chain reaction method. Results  When compared with the baseline level at the period of diagnosis before chemotherapy, the expression of miR-19b and miR-17 in AML patients increased significantly after chemotherapy. The level of miR-19b and miR-25 expression in AML patients with M3 and non-M3 French-American-British subgroups differ significantly. MiR-19b and miR-25 expression was elevated in GvHD patients, while miR-19b and miR-25 expression was somewhat decreased in GvHD patients compared with non-GvHD patients, albeit the difference was not statistically significant. Also, patients with different cytogenetic aberrations had similar levels of miR-19-b and miR-25 expression. Conclusion  MiR-19b, miR-17, and miR-25 are aberrantly expressed in AML patients' peripheral blood leukocytes, which may play a role in the development of acute GvHD following hematopoietic stem cell transplantation.

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