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자료유형
학술저널
저자정보
Yu You (Second Affiliated Hospital of Chongqing Medical University) Keting Que (Second Affiliated Hospital of Chongqing Medical University) Yun Zhou (Second Affiliated Hospital of Chongqing Medical University) Zhen Zhang (Second Affiliated Hospital of Chongqing Medical University) Xiaoping Zhao (Second Affiliated Hospital of Chongqing Medical University) Jianpin Gong (Second Affiliated Hospital of Chongqing Medical University) Zuojin Liu (Second Affiliated Hospital of Chongqing Medical University)
저널정보
한국분자세포생물학회 Molecules and Cells Molecules and Cells 제41권 제9호
발행연도
2018.9
수록면
830 - 841 (12page)

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Recent studies have indicated that microRNAs (miRNAs) play an important role in hepatocellular carcinoma (HCC) progression. In this study, we showed that miR-766-3p was decreased in approximately 72% of HCC tissues and cell lines, and its low expression level was significantly correlated with tumour size, TNM stage, metastasis, and poor prognosis in HCC. Ectopic miR-766-3p expression inhibited HCC cell proliferation, colony formation, migration and invasion. In addition, we showed that miR-766-3p repressed Wnt3a expression. A luciferase reporter assay revealed that Wnt3a was a direct target of miR-766-3p, and an inverse correlation between miR-766-3p and Wnt3a expression was observed. Moreover, Wnt3a up-regulation reversed the effects of miR-766-3p on HCC progression. In addition, our study showed that miR-766-3p up-regulation decreased the nuclear β-catenin level and expression of Wnt targets (TCF1 and Survivin) and reduced the level of MAP protein regulator of cytokinesis 1 (PRC1). However, these effects of miR-766-3p were reversed by Wnt3a up-regulation. In addition, PRC1 upregulation increased the nuclear β-catenin level and protein expression of TCF1 and Survivin. iCRT3, which disrupts the β-catenin-TCF4 interaction, repressed the TCF1, Survivin and PRC1 protein levels. Taken together, our results suggest that miR-766-3p down-regulation promotes HCC cell progression, probably by targeting the Wnt3a/PRC1 pathway, and miR-766-3p may serve as a potential therapeutic target in HCC.

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