黑色素瘤
基因沉默
癌症研究
小RNA
拮抗剂
下调和上调
癌症
生物
RNA干扰
细胞培养
转移
抑制器
MCL1
细胞
医学
核糖核酸
基因
生物化学
遗传学
作者
Claudia E.M. Weber,Chonglin Luo,Agnes Hotz‐Wagenblatt,Adriane Gardyan,Theresa Kordaß,Tim Holland‐Letz,Wolfram Osen,Stefan B. Eichmüller
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2016-04-16
卷期号:76 (12): 3562-3571
被引量:95
标识
DOI:10.1158/0008-5472.can-15-2932
摘要
Abstract Determinants of invasion and metastasis in cancer remain of great interest to define. Here, we report the definition of miR-339-3p as a novel tumor suppressive microRNA that blocks melanoma cell invasion without affecting cell survival. miR-339-3p was identified by a comprehensive functional screen of a human miRNA mimetic library in a cell-based assay for invasion by the melanoma cell line A375. miR-339-3p was determined as a strong inhibitor of invasion differentially expressed in melanoma cells and healthy melanocytes. MCL1 was defined as a target for downregulation by miR-339-3p, functioning through direct interaction with the 3′ untranslated region of MCL1 mRNA. Blocking miR-339-3p by an antagomiR was sufficient to increase melanoma cell invasion, an effect that could be phenocopied by RNAi-mediated silencing of MCL1. In vivo studies established that miR-339-3p overexpression was sufficient to decrease lung colonization by A375 melanoma cells in NSG mice, relative to control cells. Overall, our results defined miR-339-3p as a melanoma tumor suppressor, the levels of which contributes to invasive aggressiveness. Cancer Res; 76(12); 3562–71. ©2016 AACR.
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