河马信号的阴暗面:癌症启动子的作用。

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Fly Pub Date : 2017-10-02 Epub Date: 2017-06-02 DOI:10.1080/19336934.2017.1336270
Brandon Dunn, Xianjue Ma
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引用次数: 2

摘要

Hippo信号通路调节器官大小和组织稳态。鉴于这一作用,这一途径的失调对癌症进展有影响就不足为奇了。大量令人信服的文献表明,Hippo通路具有肿瘤抑制功能,其失活导致大量过度生长。然而,其他研究也表明,Hippo信号的激活可以促进肿瘤的进展。目前尚不清楚单一途径如何产生如此截然相反的效果。这种知识的缺乏部分是由于我们无法从各种细胞类型、组织和生物体的研究中进行有意义的比较。然而,最近我们发表了2篇利用果蝇翅盘研究Hippo通路的研究,发现Hippo通路激活可以促进细胞迁移和侵袭,而Hippo通路失活导致细胞过度生长。因此,我们在此提出,果蝇可以提供一个研究平台,开始研究Hippo通路如何在同一组织中促进和抑制肿瘤进展,这是由于已发表的Hippo通路的促肿瘤和抗肿瘤功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The dark side of hippo signaling: A cancer promoter role.

The dark side of hippo signaling: A cancer promoter role.

The dark side of hippo signaling: A cancer promoter role.

The Hippo signaling pathway regulates organ size and tissue homeostasis. Given this role it is unsurprising that dysregulation of this pathway has implications for cancer progression. A convincing body of literature shows that the Hippo pathway serves a tumor suppressive function with its inactivation leading to massive overgrowth. However, additional studies have also shown that activation of Hippo signaling can promote tumor progression. It remains unknown how a single pathway can produce such diametrically opposed effects. This lack of knowledge is in part due to our inability to make meaningful comparisons from studies which have taken place in a variety of cell types, tissues, and organisms. Recently however, we have published 2 studies using the Drosophila wing disk to study the Hippo pathway and have found that Hippo pathway activation can promote cell migration and invasion while Hippo pathway inactivation leads to overgrowth. Thus we propose here that Drosophila can provide a research platform with which to begin addressing how the Hippo pathway can both enhance and suppress tumor progression due to published pro- and anti-tumor functionalities of the Hippo pathway in the same tissue.

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来源期刊
Fly
Fly 生物-生化与分子生物学
CiteScore
2.90
自引率
0.00%
发文量
17
审稿时长
>12 weeks
期刊介绍: Fly is the first international peer-reviewed journal to focus on Drosophila research. Fly covers a broad range of biological sub-disciplines, ranging from developmental biology and organogenesis to sensory neurobiology, circadian rhythm and learning and memory, to sex determination, evolutionary biology and speciation. We strive to become the “to go” resource for every researcher working with Drosophila by providing a forum where the specific interests of the Drosophila community can be discussed. With the advance of molecular technologies that enable researchers to manipulate genes and their functions in many other organisms, Fly is now also publishing papers that use other insect model systems used to investigate important biological questions. Fly offers a variety of papers, including Original Research Articles, Methods and Technical Advances, Brief Communications, Reviews and Meeting Reports. In addition, Fly also features two unconventional types of contributions, Counterpoints and Extra View articles. Counterpoints are opinion pieces that critically discuss controversial papers questioning current paradigms, whether justified or not. Extra View articles, which generally are solicited by Fly editors, provide authors of important forthcoming papers published elsewhere an opportunity to expand on their original findings and discuss the broader impact of their discovery. Extra View authors are strongly encouraged to complement their published observations with additional data not included in the original paper or acquired subsequently.
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