a Department of Internal Medical , São Paulo State University (UNESP-FMB) , Botucatu , SP , Brazil.
b Laboratory of Molecular Biology , Hospital Dr. Amaral Carvalho , Jahu , SP , Brazil.
Leuk Lymphoma. 2019 Mar;60(3):805-811. doi: 10.1080/10428194.2018.1499905. Epub 2018 Sep 6.
Chronic myeloid leukemia (CML) is a stem cell derived malignant disorder result of translocation t(9;22)(q34;q11) called Philadelphia chromosome (Ph). microRNAS (miRNAs) are involved in several biological processes, altering the progression of various pathologies, including CML. This study evaluated whether circulating miRNAs display differential expression profiles in peripheral blood of CML-Chronic Phase (CML-CP) patients newly diagnosed in comparison with CML-CP treated with imatinib. We obtained peripheral blood samples from CML-CP Ph patients divided among group 1 (untreated newly diagnosed) and group 2 (treated with imatinib). A pool of total leukocytes from healthy donors was considered as control group. Expression analyses were performed for 768 miRNAs by RT-qPCR array. Bioinformatic tools were used to identify significant pathways and interaction networks. We found 80 deregulated miRNAs between the groups and, according to bioinformatic analysis, they are involved in different pathways, including molecular mechanisms of cancer. The study allows better understanding of disease molecular behavior, and it is useful for possible monitoring CML treatment and prognostic biomarkers identification.
慢性髓性白血病(CML)是一种源于干细胞的恶性疾病,其特征是发生易位 t(9;22)(q34;q11),即费城染色体(Ph)。微小 RNA(miRNAs)参与了多种生物学过程,改变了包括 CML 在内的各种病理的进展。本研究评估了新诊断的 CML-慢性期(CML-CP)患者外周血中循环 miRNA 是否存在差异表达谱,并与接受伊马替尼治疗的 CML-CP 患者进行了比较。我们从 CML-CP Ph 患者中获得了外周血样本,分为 1 组(未经治疗的新诊断)和 2 组(接受伊马替尼治疗)。将来自健康供体的总白细胞池作为对照组。通过 RT-qPCR 阵列对 768 种 miRNA 进行了表达分析。使用生物信息学工具来识别显著的途径和相互作用网络。我们发现两组之间有 80 种失调的 miRNA,根据生物信息学分析,它们涉及不同的途径,包括癌症的分子机制。该研究有助于更好地了解疾病的分子行为,并且对于可能的 CML 治疗监测和预后生物标志物的识别是有用的。