死盒RNA解旋酶:乳腺癌的microRNA管理者

Wanpei Cai, Chao Wang, J. N. Goh, S. Loo, C. Yap, A. Kumar
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引用次数: 2

摘要

近年来,非编码RNA,尤其是microRNA在癌症中的作用引起了人们对RNA研究领域的兴趣。随着非编码RNA研究的发现,曾经被广泛接受的描述细胞蛋白质表达流程的“遗传学中心教条”现在正受到挑战。mirna属于非编码rna家族,其中许多已被证明与包括乳腺癌在内的癌症进展有关。Goh等人最近全面总结了mirna在乳腺癌进展标志中的作用。在本研究重点中,我们简要总结了这些mirna在乳腺癌进展中的相关标志,并重点介绍了一个被称为DEAD-box RNA解旋酶的蛋白家族,其中许多已被发现与mirna相关的肿瘤发生有关。近年来,关于DEAD-box RNA解旋酶的研究越来越多,在许多癌症类型中报道了不同的作用。DDX20是DEAD-box RNA解旋酶家族的一员,最近被我们的研究小组发现参与乳腺癌的进展和转移。我们小组的新数据发现DDX20在乳腺癌中可能具有新的mirna加工作用。在一项正在进行的研究中,我们发现miRNA miR-222的表达与DDX20呈负相关,这表明miR-222在浸润性乳腺癌中可能具有抑瘤作用,这与之前报道miR-222与乳腺癌侵袭性相关的报道相反。因此,我们的工作为复杂性提供了另一个维度,即mirna和DEAD-box RNA解旋酶在乳腺癌中的作用。
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DEAD-box RNA Helicases: the microRNA managers of breast cancer
The roles of non-coding RNAs in cancers, microRNA (miRNA) especially, have sparked interest in the field of RNA research in recent years. The once widely accepted ‘central dogma of genetics’ describing the flow of cellular protein expression is now being challenged following the discovery of non-coding RNA research. miRNAs belong to the family of non-coding RNAs, in which many have been shown to be involved in cancer progression, including breast cancer. Goh et al. have recently summarized comprehensively, the roles of miRNAs in the hallmarks of breast cancer progression. In this research highlight, we provide a brief summary of these miRNA-associated hallmarks in breast cancer progression and also highlight on a family of proteins known as DEAD-box RNA helicases, many of which have been found to be associated with miRNA-associated tumorigenesis. There are an increasing number of studies on DEAD-box RNA helicases in recent years, with different roles being reported in numerous cancer types. DDX20, a member of the DEAD-box RNA helicase family, was most recently identified by our group to be involved in breast cancer progression and metastasis. New data from our group found a possible novel miRNA-processing role of DDX20 in breast cancer. In an ongoing study, we found miRNA miR-222 expression inversely correlates with DDX20, suggesting a possible tumor suppressor role of miR-222 in invasive breast cancers, contrary to previous reports where miR-222 was associated with invasion in breast cancers. Our work thus provides another dimension to the complexity, where miRNAs and DEAD-box RNA helicases play in breast cancers.
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