MiR-218 Inhibits Invasion and Metastasis of Gastric Cancer by Targeting the Robo1 Receptor

Jun Tie(Air Force Medical University), Yanglin Pan(Xijing Hospital), Lina Zhao(Xijing Hospital), Kaichun Wu(Air Force Medical University), Jie Liu(Xijing Hospital), Shiren Sun(Xijing Hospital), Xuegang Guo(Xijing Hospital), Biaoluo Wang(Air Force Medical University), Gang Yi(Air Force Medical University), Yongguo Zhang(Air Force Medical University), Quanjiang Li(Air Force Medical University), Taidong Qiao(Air Force Medical University), Qingchuan Zhao(Air Force Medical University), Yongzhan Nie(Xijing Hospital), Daiming Fan(Air Force Medical University)
PLoS Genetics
March 11, 2010
Cited by 446Open Access
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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.


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