State Key Laboratory of Cancer Biology and Xijing Hospital of Digestive Diseases, Fourth Military Medical University, Xi'an, Shaanxi, China.
PLoS Genet. 2010 Mar 12;6(3):e1000879. doi: 10.1371/journal.pgen.1000879.
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.
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。