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microRNA expression profile and identification of miR-29 as a prognostic marker and pathogenetic factor by targeting CDK6 in mantle cell lymphoma

机译:靶向CDK6在套细胞淋巴瘤中的microRNA表达谱及miR-29作为预后标志物和致病因子的鉴定

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摘要

Mantle cell lymphoma (MCL) is one of the most aggressive B-cell lymphomas. Although several protein-coding genes are altered, expression signature and importance of microRNA (miRNA) have not been well documented in this malignancy. Here, we performed miRNA expression profile in 30 patients with MCL using a platform containing 515 human miRNAs. Eighteen miRNAs were down-regulated and 21 were up-regulated in MCL compared with normal B lymphocytes. The most frequently altered miRNAs are decrease of miR-29a/b/c, miR-142-3p/5p, and miR-150 and increase of miR-124a and miR-155. Notably, expression levels of miR-29 family are associated with prognosis. The patients with significant down-regulated miR-29 had short survival compared with those who express relatively high levels of miR-29. The prognostic value of miR-29 is comparable with the Mantle Cell Lymphoma International Prognostic Index. Furthermore, we demonstrate miR-29 inhibition of CDK6 protein and mRNA levels by direct binding to 3′-untranslated region. Inverse correlation between miR-29 and CDK6 was observed in MCL. Because cyclin D1 overexpression is a primary event and exerts its function through activation of CDK4/CDK6, our results in primary MCL cells indicate that down-regulation of miR-29 could cooperate with cyclin D1 in MCL pathogenesis. Thus, our findings provide not only miRNA expression signature but also a novel prognostic marker and pathogenetic factor for this malignancy.
机译:套细胞淋巴瘤(MCL)是最具侵略性的B细胞淋巴瘤之一。尽管几个蛋白质编码基因发生了改变,但在这种恶性肿瘤中尚未充分证明microRNA(miRNA)的表达特征和重要性。在这里,我们使用包含515个人类miRNA的平台对30例MCL患者进行了miRNA表达谱分析。与正常B淋巴细胞相比,MCL中有18个miRNA下调,有21个上调。改变最频繁的miRNA是miR-29a / b / c,miR-142-3p / 5p和miR-150的减少以及miR-124a和miR-155的增加。值得注意的是,miR-29家族的表达水平与预后相关。与表达相对较高miR-29水平的患者相比,miR-29水平显着下调的患者生存期较短。 miR-29的预后价值与Mantle细胞淋巴瘤国际预后指数相当。此外,我们证明了直接结合到3'-非翻译区,miR-29对CDK6蛋白和mRNA水平的抑制。在MCL中观察到miR-29与CDK6呈负相关。由于细胞周期蛋白D1的过表达是主要事件,并且通过激活CDK4 / CDK6发挥其功能,因此我们在原代MCL细胞中的结果表明,miR-29的下调可能与细胞周期蛋白D1在MCL发病机理中协同作用。因此,我们的发现不仅为该恶性肿瘤提供了miRNA表达特征,而且还提供了一种新的预后标志物和致病因素。

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