Deng Xianzhao, Wu Bo, Xiao Ke, Kang Jie, Xie Jing, Zhang Xiaoping, Fan Youben
Center of Thyroid and Parathyroid, Department of General Surgery, Shanghai Sixth People's Hospital, Shanghai Jiaotong University of Medicine, Shanghai, China.
Cell Physiol Biochem. 2015;35(1):71-82. doi: 10.1159/000369676. Epub 2015 Jan 2.
BACKGROUND/AIMS: Micro-RNA (miR)-146b-5p is overexpressed in papillary thyroid carcinoma (PTC) and associated with extrathyroidal invasion and advanced tumor stage. In the present study, we showed that miR-146b-5p is upregulated in PTC with lymph node metastasis.
A computational search and luciferase assay identified zinc RING finger 3 (ZNRF3), a negative regulator of Wnt/β-catenin signaling, as a direct target of miR-146b-5p in PTC.
MiR-146b-5p promoted migration and invasiveness and induced epithelial-mesenchymal transition (EMT) of PTC cells, whereas ZNRF3 overexpression reversed this effect. MiR-146b-5p increased the cell surface levels of the Wnt receptors Frizzled-6 and LRP6 and enhanced Wnt/β-catenin signaling by downregulating ZNRF3, whereas an inhibitor of Wnt/β-catenin suppressed the effect of miR-146b-5p on migration, invasiveness and EMT of PTC cells.
These results indicate that miR-146b-5p induces EMT and may promote PTC metastasis through the regulation of Wnt/β-catenin signaling, and suggest novel potential therapeutic targets for the treatment of PTC.
背景/目的:微小RNA(miR)-146b-5p在甲状腺乳头状癌(PTC)中过表达,且与甲状腺外侵犯及肿瘤晚期相关。在本研究中,我们发现miR-146b-5p在伴有淋巴结转移的PTC中上调。
通过计算机搜索和荧光素酶检测确定锌指环蛋白3(ZNRF3)作为PTC中miR-146b-5p的直接靶点,ZNRF3是Wnt/β-连环蛋白信号通路的负调节因子。
miR-146b-5p促进PTC细胞的迁移和侵袭,并诱导上皮-间质转化(EMT),而ZNRF3过表达可逆转这种作用。miR-146b-5p通过下调ZNRF3增加Wnt受体卷曲蛋白6(Frizzled-6)和低密度脂蛋白受体相关蛋白6(LRP6)的细胞表面水平,并增强Wnt/β-连环蛋白信号通路,而Wnt/β-连环蛋白抑制剂可抑制miR-146b-5p对PTC细胞迁移、侵袭和EMT的影响。
这些结果表明,miR-146b-5p通过调节Wnt/β-连环蛋白信号通路诱导EMT并可能促进PTC转移,并提示了治疗PTC的新的潜在治疗靶点。