尼洛替尼改变的microRNA表达模式在伊马替尼耐药慢性髓性白血病细胞中的鉴定

Ren-In You , Ching-Liang Ho , Hsiu-Man Hung , Tsu-Yi Chao
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引用次数: 2

摘要

耐药是血液病和其他恶性肿瘤治疗失败的关键因素。尼洛替尼已被观察到对伊马替尼治疗失败或不耐受的慢性期慢性髓性白血病(CML)患者具有显著的活性。最近的报道表明,microRNA (miRNA)的表达变化参与了人类癌症的药物反应。先前已经发现一些mirna在伊马替尼耐药中持续失调;然而,伊马替尼治疗失败的尼洛替尼患者的信息非常有限。许多报道已经发现循环mirna作为疾病和治疗反应的非侵入性生物标志物。本研究的目的是探索miRNA的调控,寻找CML的候选miRNA标记物,可用于药物反应预测。在这里,我们通过微阵列芯片分析展示了伊马替尼耐药K562 CML细胞(K562- r)培养上清中的循环miRNA谱。我们通过比较尼洛替尼处理的K562-R细胞培养上清和未处理的K562-R细胞培养上清的miRNA表达模式,确定了与尼洛替尼敏感性相关的特异性miRNA。从本研究中获得的信息可能有潜力成为未来预测药物反应的新型生物标志物,也可以应用于开发新的CML治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of nilotinib-altered microRNA expression patterns in imatinib-resistant chronic myeloid leukemia cells

Drug resistance is a key contributor for treatment failure in hematologic and other malignancies. Nilotinib has been observed with significant activity in patients with chronic phase chronic myeloid leukemia (CML) who have failed or are intolerant of imatinib therapy. Recent reports have suggested that microRNA (miRNA) expression changes are involved in the drug response of human cancer. Several miRNAs have been previously found to be consistently deregulated in imatinib resistance; however, very limited information is available for nilotinib-treated patients who have failed imatinib therapy. Many reports have discovered circulating miRNAs as noninvasive biomarkers of disease and therapy response. The aim of this study was to explore miRNA regulation and find candidate miRNA markers for CML that can be used for drug response prediction. Here we demonstrate the circulating miRNA profile in the culture supernatant of imatinib-resistant K562 CML cells (K562-R) by microarray chip analysis. We have identified specific miRNAs that are associated with nilotinib sensitivity by comparison of miRNA expression patterns from the culture supernatant of nilotinib-treated K562-R cells with the culture supernatant of untreated K562-R cells. The information obtained from this study may have the potential to become a novel biomarker to predict drug response in the future and can also be applied to developing novel therapeutic treatment for CML.

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