Division of Pulmonary and Critical Care Sciences, School of Medicine, University of Colorado, Anschutz Medical Campus , Aurora, CO 80045 , USA.
Biol Open. 2013 May 22;2(7):675-85. doi: 10.1242/bio.20134507. Print 2013 Jul 15.
In non-small cell lung cancer cell lines, activation of β-catenin independent signaling, via Wnt7a/Frizzled9 signaling, leads to reversal of cellular transformation, reduced anchorage-independent growth and induction of epithelial differentiation. miRNA expression profiling on a human lung adenocarcinoma cell line (A549) identified hsa-miR29b as an important downstream target of Wnt7a/Frizzled9 signaling. We show herein that hsa-miR29b expression is lost in non-small cell lung cancer (NSCLC) cell lines and stimulation of β-catenin independent signaling, via Wnt7a expression, in NSCLC cell lines results in increased expression of hsa-miR29b. Surprisingly, we also identify specific regulation of hsa-miR29b by Wnt7a but not by Wnt3, a ligand for β-catenin-dependent signaling. Interestingly, knockdown of hsa-miR29b was enough to abrogate the tumor suppressive effects of Wnt7a/Frizzled9 signaling in NSCLC cells, suggesting that hsa-miR29b is an important mediator of β-catenin independent signaling. Finally, we show for the first time that hsa-miR29b plays an important role as a tumor suppressor in lung cancer by targeting murine double mutant 2 (MDM2), revealing novel nodes for Wnt7a/Frizzled9-mediated regulation of NSCLC cell proliferation.
在非小细胞肺癌细胞系中,通过 Wnt7a/Frizzled9 信号转导激活β-catenin 非依赖性信号转导,导致细胞转化逆转、锚定非依赖性生长减少和上皮分化诱导。对人肺腺癌细胞系(A549)进行 miRNA 表达谱分析,鉴定出 hsa-miR29b 是 Wnt7a/Frizzled9 信号转导的重要下游靶标。本文研究表明,hsa-miR29b 在非小细胞肺癌(NSCLC)细胞系中表达缺失,Wnt7a 表达刺激 NSCLC 细胞系中β-catenin 非依赖性信号转导,导致 hsa-miR29b 表达增加。令人惊讶的是,我们还发现 hsa-miR29b 受到 Wnt7a 的特异性调节,而不是β-catenin 依赖性信号转导配体 Wnt3 的调节。有趣的是,hsa-miR29b 的敲低足以消除 Wnt7a/Frizzled9 信号转导在 NSCLC 细胞中的肿瘤抑制作用,表明 hsa-miR29b 是β-catenin 非依赖性信号转导的重要介质。最后,我们首次证明 hsa-miR29b 通过靶向鼠双突变体 2(MDM2)在肺癌中作为肿瘤抑制因子发挥重要作用,揭示了 Wnt7a/Frizzled9 介导的 NSCLC 细胞增殖调控的新节点。