果蝇中脑的不对称干细胞分裂:与肿瘤发生的关系。

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Fly Pub Date : 2018-01-02 Epub Date: 2018-01-08 DOI:10.1080/19336934.2017.1416277
Ana Carmena
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引用次数: 6

摘要

不对称细胞分裂(ACD)是细胞发育过程中产生细胞多样性的重要过程。此外,最近ACD、癌症和干细胞生物学之间的联系在该领域开辟了新的、非常有趣的领域。十多年前,ACD受损与肿瘤发生之间的联系首次在果蝇神经干细胞(神经母细胞,NBs)中得到证实,在过去的几年里,它也在脊椎动物干细胞中得到证实。本文以果蝇幼虫脑NBs为研究对象,根据我们实验室最近获得的结果,我们重新审视了这一联系,强调了两个主要方面:1)不同ACD调节因子抑瘤活性的差异;2)环境和时间窗框架与ACD依赖性诱导肿瘤样过度生长的潜在相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Compromising asymmetric stem cell division in Drosophila central brain: Revisiting the connections with tumorigenesis.

Compromising asymmetric stem cell division in Drosophila central brain: Revisiting the connections with tumorigenesis.

Compromising asymmetric stem cell division in Drosophila central brain: Revisiting the connections with tumorigenesis.

Compromising asymmetric stem cell division in Drosophila central brain: Revisiting the connections with tumorigenesis.

Asymmetric cell division (ACD) is an essential process during development for generating cell diversity. In addition, a more recent connection between ACD, cancer and stem cell biology has opened novel and highly intriguing venues in the field. This connection between compromised ACD and tumorigenesis was first demonstrated using Drosophila neural stem cells (neuroblasts, NBs) more than a decade ago and, over the past years, it has also been established in vertebrate stem cells. Here, focusing on Drosophila larval brain NBs, and in light of results recently obtained in our lab, we revisit this connection emphasizing two main aspects: 1) the differences in tumor suppressor activity of different ACD regulators and 2) the potential relevance of environment and temporal window frame for compromised ACD-dependent induction of tumor-like overgrowth.

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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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