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转化生长因子-β与微小RNA:上皮可塑性中的mRNA调控网络

Transforming growth factor-beta and microRNA:mRNA regulatory networks in epithelial plasticity.

作者信息

Zavadil Jiri, Narasimhan Manisha, Blumenberg Miroslav, Schneider Robert J

机构信息

Department of Pathology and NYU Cancer Institute, New York University School of Medicine, New York, NY 10016, USA.

出版信息

Cells Tissues Organs. 2007;185(1-3):157-61. doi: 10.1159/000101316.

Abstract

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.

摘要

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。

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