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Dicer 在卵巢癌中的表达与预后的关系——与全球 miRNA 变化和雌激素受体表达的关系。

Prognostic significance of Dicer expression in ovarian cancer-link to global microRNA changes and oestrogen receptor expression.

机构信息

Institute of Pathology, Charité University Hospital, 10117 Berlin, Germany.

出版信息

J Pathol. 2010 Feb;220(3):382-91. doi: 10.1002/path.2658.

DOI:10.1002/path.2658
PMID:19960504
Abstract

MicroRNA (miRNA) deregulation is a hallmark of human cancer. However, the mechanisms underlying miRNA alteration and the specific role of proteins involved in miRNA processing remains to be elucidated. Dicer is a key enzyme in the miRNA processing pathway that is essential for the production of mature miRNAs from their precursors. We tested the hypothesis that Dicer has biological and clinical relevance in ovarian cancer, using a range of methods including in vitro manipulation of Dicer expression. We observed down-regulation of Dicer in a subgroup of ovarian carcinomas, and found that decreased Dicer expression correlates significantly with reduced patient survival in serous cancers and advanced disease stages. Moreover, microarray and functional analysis suggest that reduced Dicer expression is connected with a global down-regulation of the microRNAome and with gene expression changes, particularly reduced expression of oestrogen receptor (ER) mRNA and protein in tumour tissue and in cell culture. Our data suggest a common mechanism for miRNAs changes by alterations in the basic machinery controlling miRNA biogenesis, of which Dicer is a central enzyme. These alterations of miRNA processing are of prognostic value and may play a role in the molecular pathogenesis of ovarian carcinoma and, possibly, other tumours. Knowledge of these molecular pathways may help toward new targeted therapeutic approaches for ovarian cancer.

摘要

MicroRNA (miRNA) 失调是人类癌症的一个标志。然而,miRNA 改变的机制以及参与 miRNA 加工的蛋白质的具体作用仍有待阐明。Dicer 是 miRNA 加工途径中的关键酶,对于从其前体产生成熟 miRNA 至关重要。我们使用一系列方法,包括体外操纵 Dicer 表达,检验了 Dicer 在卵巢癌中具有生物学和临床相关性的假设。我们观察到在一小部分卵巢癌中存在 Dicer 的下调,并且发现 Dicer 表达的降低与浆液性癌和晚期疾病阶段患者生存率的降低显著相关。此外,微阵列和功能分析表明,Dicer 表达的降低与 microRNAome 的整体下调以及基因表达变化有关,特别是肿瘤组织和细胞培养物中雌激素受体 (ER) mRNA 和蛋白质的表达降低有关。我们的数据表明,通过改变控制 miRNA 生物发生的基本机制,存在 miRNA 变化的共同机制,其中 Dicer 是一种核心酶。这些 miRNA 加工的改变具有预后价值,可能在卵巢癌和可能的其他肿瘤的分子发病机制中发挥作用。对这些分子途径的了解可能有助于为卵巢癌开发新的靶向治疗方法。

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