| Literature DB >> 27197185 |
Claudia E M Weber1, Chonglin Luo1, Agnes Hotz-Wagenblatt2, Adriane Gardyan1, Theresa Kordaß1, Tim Holland-Letz3, Wolfram Osen1, Stefan B Eichmüller4.
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. ©2016 American Association for Cancer Research.Entities:
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Year: 2016 PMID: 27197185 DOI: 10.1158/0008-5472.CAN-15-2932
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701