College of Life Sciences and Laboratory for Marine Biology and Biotechnology of Qingdao National Laboratory for Marine Science and Technology, Zhejiang University, Hangzhou, People's Republic of China.
Cancer Res. 2017 Oct 15;77(20):5543-5553. doi: 10.1158/0008-5472.CAN-17-1375. Epub 2017 Aug 30.
Cross-species regulation of gene expression by microRNA is a possible untapped opportunity for miRNA-based therapy. In this study, we report a novel approach to ablate melanoma stem-like cells by targeting the transcription factor YB-1, which is significantly and selectively upregulated in these cells in melanoma. Silencing YB-1 expression was sufficient to significantly inhibit the stemness of melanoma stem-like cells. In exploring YB-1 targeting, we discovered that the shrimp microRNA miR-S8 could suppress human YB-1 expression in melanoma stem-like cells. Mechanistic investigations revealed that miR-S8 recognized the 3'UTR of YB-1 mRNA and mediated its degradation. In tumor cell and xenograft experiments, miR-S8 suppressed the tumorigenic capacity of melanoma stem-like cells by targeting human YB-1. Overall, our results illuminated a novel aspect of miRNA-mediated cross-species gene expression and its use in regulating cancer stem-like cells. .
miRNA 介导的种间基因表达调控可能是 miRNA 治疗的一个未被开发的机会。在这项研究中,我们报告了一种通过靶向转录因子 YB-1 来消除黑色素瘤干细胞样细胞的新方法,YB-1 在黑色素瘤中这些细胞中显著且选择性地上调。沉默 YB-1 的表达足以显著抑制黑色素瘤干细胞样细胞的干性。在探索 YB-1 的靶向作用时,我们发现虾 microRNA miR-S8 可以抑制黑色素瘤干细胞样细胞中的人 YB-1 表达。机制研究表明,miR-S8 通过识别 YB-1 mRNA 的 3'UTR 并介导其降解来靶向 YB-1。在肿瘤细胞和异种移植实验中,miR-S8 通过靶向人 YB-1 抑制了黑色素瘤干细胞样细胞的致瘤能力。总之,我们的研究结果揭示了 miRNA 介导的种间基因表达调控及其在调控癌症干细胞样细胞中的新作用。