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转化生长因子-β调控的微小RNA及其在癌症生物学中的功能

TGF-β-Regulated MicroRNAs and Their Function in Cancer Biology.

作者信息

Yang Pengyuan, Zhang Yun, Markowitz Geoffrey J, Guo Xing, Wang Xiao-Fan

机构信息

CAS Key Laboratory of Infection and Immunity, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.

Department of Pharmacology and Cancer Biology, Duke University Medical Center, 3813, Research Drive, Durham, NC, 27710, USA.

出版信息

Methods Mol Biol. 2016;1344:325-39. doi: 10.1007/978-1-4939-2966-5_21.

Abstract

The transforming growth factor-β (TGF-β) is known to regulate a large number of biological processes and is involved in various aspects of tumor development. Recent studies have shown that the biogenesis of miRNAs can be regulated by TGF-β signaling directly via Smad-dependent mechanisms and/or other unknown mechanisms, which may induce autoregulatory feedback loops in response to the activation of TGF-β signaling, influencing the fate of tumor cells. In this chapter, we summarize the currently described mechanisms underlying TGF-β's regulation of miRNA biogenesis, and the functional role of TGF-β-regulated miRNAs in tumor initiation, epithelial-mesenchymal transition, and tumor microenvironment modulation. Finally, we introduce methods to study TGF-β-regulated miRNAs and their functions in tumor progression and metastasis using an example of publication from our lab demonstrating the presence of a TGF-β-miR-34a-CCL22 signaling axis, which serves as a potent etiological pathway for the development of hepatocellular carcinoma venous metastases.

摘要

已知转化生长因子-β(TGF-β)可调节大量生物学过程,并参与肿瘤发展的各个方面。最近的研究表明,miRNA的生物合成可通过TGF-β信号通路直接经由Smad依赖机制和/或其他未知机制进行调节,这可能会在TGF-β信号通路激活时诱导自调节反馈回路,从而影响肿瘤细胞的命运。在本章中,我们总结了目前所描述的TGF-β调节miRNA生物合成的潜在机制,以及TGF-β调节的miRNA在肿瘤起始、上皮-间质转化和肿瘤微环境调节中的功能作用。最后,我们以我们实验室发表的一篇文章为例,介绍研究TGF-β调节的miRNA及其在肿瘤进展和转移中的功能的方法,该文章证明了TGF-β-miR-34a-CCL22信号轴的存在,它是肝细胞癌静脉转移发生的一条重要病因途径。

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