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首页> 外文期刊>Critical reviews in clinical laboratory sciences >Exosome-carried microRNA-based signature as a cellular trigger for the evolution of chronic lymphocytic leukemia into Richter syndrome
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Exosome-carried microRNA-based signature as a cellular trigger for the evolution of chronic lymphocytic leukemia into Richter syndrome

机译:外部携带的微小RORNA的签名作为慢性淋巴细胞白血病演变为RECHTER综合征的细胞触发

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摘要

Even if considered a cumulative and not a proliferative CD5+ B-cell neoplasm, chronic lymphocytic leukemia (CLL) has a proliferation rate higher than that recognized earlier, especially in the lymphoid tissues. Some patients with CLL develop a clinical syndrome entitled Richter syndrome (RS). Understanding CLL genetics and epigenetics may help to elucidate the molecular basics of the clinical heterogeneity of this type of malignancy. In the present project we aimed to identify a microRNA species that can predict the evolution of therapy-resistant CLL towards RS. In the first phase of our study, microRNA-19b was identified as a possible target, and in the second phase, we transfected three different CLL cell lines with microRNA-19b mimic and inhibitor and assessed the potential role on leukemia cells in vitro. The mechanism by which miR-19b acts were identified as the upregulation of Ki67 and downregulation of p53. This was further supported through RT-PCR and western blotting on CLL cell lines, as well as by next generation sequencing on two patients diagnosed with CLL that evolved into RS.
机译:即使考虑了累积而不是增殖性CD5 + B细胞肿瘤,慢性淋巴细胞白血病(CLL)也具有比前面识别的增殖率,特别是在淋巴组织中。一些CLL患者开发了题为Richter综合征(RS)的临床综合症。了解CLL遗传学和表观遗传学可能有助于阐明这种恶性肿瘤的临床异质性的分子基础。在目前的项目中,我们旨在鉴定一种可以预测治疗抗性CLL的微小肠物种朝向卢比的演变。在我们研究的第一阶段,MicroRNA-19B被鉴定为可能的靶标,在第二阶段中,我们用MicroRNA-19B模拟物和抑制剂转染三种不同的CLL细胞系,并评估体外白血病细胞上的潜在作用。 miR-19b作用的机制被鉴定为Ki67的上调和P53的下调。通过RT-PCR和Western印迹进一步支持CL1细胞系,以及通过诊断为Rs的CLL的两名患者进行下一代测序。

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