Zavadil Jiri, Narasimhan Manisha, Blumenberg Miroslav, Schneider Robert J
Department of Pathology and NYU Cancer Institute, New York University School of Medicine, New York, NY 10016, USA.
Cells Tissues Organs. 2007;185(1-3):157-61. doi: 10.1159/000101316.
Noncoding microRNAs act as posttranscriptional repressors of gene function and are often deregulated in cancers and other diseases. Here we review recent findings on microRNA roles in tumorigenesis and report a microRNA profiling screen in transforming growth factor-beta1 (TGF-beta)-induced epithelial-mesenchymal transition (EMT) in human keratinocytes, a model of epithelial cell plasticity underlying epidermal injury and skin carcinogenesis. We describe a novel EMT-specific microRNA signature that includes induction of miR-21, a candidate oncogenic microRNA associated with carcinogenesis. By integrating the microRNA screen results with target prediction algorithms and gene expression profiling data, we outline a framework for TGF-beta-directed microRNA:messenger RNA (mRNA) regulatory circuitry and discuss its biological relevance for tumor progression.
非编码微小RNA作为基因功能的转录后抑制因子,在癌症和其他疾病中常常失调。在此,我们综述了关于微小RNA在肿瘤发生中作用的最新研究发现,并报告了一项在人角质形成细胞中进行的微小RNA谱筛选,该细胞在转化生长因子-β1(TGF-β)诱导的上皮-间质转化(EMT)过程中发生变化,此过程是表皮损伤和皮肤癌发生所涉及的上皮细胞可塑性模型。我们描述了一种新的EMT特异性微小RNA特征,其中包括致癌候选微小RNA miR-21的诱导。通过将微小RNA筛选结果与靶标预测算法及基因表达谱数据相结合,我们勾勒出了TGF-β导向的微小RNA:信使核糖核酸(mRNA)调控回路的框架,并讨论了其与肿瘤进展的生物学相关性。