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miR-218 通过靶向 Robo1 受体抑制胃癌的侵袭和转移。

MiR-218 inhibits invasion and metastasis of gastric cancer by targeting the Robo1 receptor.

机构信息

State Key Laboratory of Cancer Biology and Xijing Hospital of Digestive Diseases, Fourth Military Medical University, Xi'an, Shaanxi, China.

出版信息

PLoS Genet. 2010 Mar 12;6(3):e1000879. doi: 10.1371/journal.pgen.1000879.

Abstract

MicroRNAs play key roles in tumor metastasis. Here, we describe the regulation and function of miR-218 in gastric cancer (GC) metastasis. miR-218 expression is decreased along with the expression of one of its host genes, Slit3 in metastatic GC. However, Robo1, one of several Slit receptors, is negatively regulated by miR-218, thus establishing a negative feedback loop. Decreased miR-218 levels eliminate Robo1 repression, which activates the Slit-Robo1 pathway through the interaction between Robo1 and Slit2, thus triggering tumor metastasis. The restoration of miR-218 suppresses Robo1 expression and inhibits tumor cell invasion and metastasis in vitro and in vivo. Taken together, our results describe a Slit-miR-218-Robo1 regulatory circuit whose disruption may contribute to GC metastasis. Targeting miR-218 may provide a strategy for blocking tumor metastasis.

摘要

微小 RNA 在肿瘤转移中发挥着关键作用。在这里,我们描述了 miR-218 在胃癌(GC)转移中的调控和功能。miR-218 的表达随着其宿主基因之一 Slit3 在转移性 GC 中的表达而降低。然而,Slit 的几个受体之一 Robo1 受到 miR-218 的负调控,从而建立了一个负反馈回路。miR-218 水平的降低消除了 Robo1 的抑制,通过 Robo1 与 Slit2 的相互作用激活 Slit-Robo1 通路,从而引发肿瘤转移。恢复 miR-218 抑制 Robo1 表达,并抑制体外和体内肿瘤细胞侵袭和转移。总之,我们的结果描述了一个 Slit-miR-218-Robo1 调节回路,其破坏可能有助于 GC 转移。靶向 miR-218 可能为阻断肿瘤转移提供一种策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11f4/2837402/a67f2eb75b78/pgen.1000879.g001.jpg

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