| Literature DB >> 28356515 |
Yoshiaki Ito1, Atsushi Inoue2, Timothy Seers1,3, Yukari Hato4, Arisa Igarashi2, Tatsuya Toyama4, Konstantin D Taganov5, Mark P Boldin6, Hiroshi Asahara7,2,8,9.
Abstract
miRNAs play critical roles in various biological processes by targeting specific mRNAs. Current approaches to identifying miRNA targets are insufficient for elucidation of a miRNA regulatory network. Here, we created a cell-based screening system using a luciferase reporter library composed of 4,891 full-length cDNAs, each of which was integrated into the 3' UTR of a luciferase gene. Using this reporter library system, we conducted a screening for targets of miR-34a, a tumor-suppressor miRNA. We identified both previously characterized and previously uncharacterized targets. miR-34a overexpression in MDA-MB-231 breast cancer cells repressed the expression of these previously unrecognized targets. Among these targets, GFRA3 is crucial for MDA-MB-231 cell growth, and its expression correlated with the overall survival of patients with breast cancer. Furthermore, GFRA3 was found to be directly regulated by miR-34a via its coding region. These data show that this system is useful for elucidating miRNA functions and networks.Entities:
Keywords: breast cancer; miR-34a; microRNA target screening; reporter library system
Mesh:
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Year: 2017 PMID: 28356515 PMCID: PMC5393199 DOI: 10.1073/pnas.1620019114
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205