轴突引导
环岛
狭缝
生物
神经系统
肿瘤进展
神经科学
电池类型
细胞生物学
癌细胞
奈特林
血管生成
细胞迁移
跨膜蛋白
癌症
细胞
轴突
受体
癌症研究
遗传学
作者
Mimmi S. Ballard,Lindsay Hinck
出处
期刊:Advances in Cancer Research
日期:2012-01-01
卷期号:: 187-235
被引量:88
标识
DOI:10.1016/b978-0-12-386503-8.00005-3
摘要
The Slit family of secreted proteins and their transmembrane receptor, Robo, were originally identified in the nervous system where they function as axon guidance cues and branching factors during development. Since their discovery, a great number of additional roles have been attributed to Slit/Robo signaling, including regulating the critical processes of cell proliferation and cell motility in a variety of cell and tissue types. These processes are often deregulated during cancer progression, allowing tumor cells to bypass safeguarding mechanisms in the cell and the environment in order to grow and escape to new tissues. In the past decade, it has been shown that the expression of Slit and Robo is altered in a wide variety of cancer types, identifying them as potential therapeutic targets. Further, studies have demonstrated dual roles for Slits and Robos in cancer, acting as both oncogenes and tumor suppressors. This bifunctionality is also observed in their roles as axon guidance cues in the developing nervous system, where they both attract and repel neuronal migration. The fact that this signaling axis can have opposite functions depending on the cellular circumstance make its actions challenging to define. Here, we summarize our current understanding of the dual roles that Slit/Robo signaling play in development, epithelial tumor progression, and tumor angiogenesis.
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