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Identification of targets of tumor suppressor microRNA-34a using a reporter library system.
Ito, Yoshiaki; Inoue, Atsushi; Seers, Timothy; Hato, Yukari; Igarashi, Arisa; Toyama, Tatsuya; Taganov, Konstantin D; Boldin, Mark P; Asahara, Hiroshi.
Afiliação
  • Ito Y; Department of Systems BioMedicine, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Bunkyo, Tokyo 113-8519, Japan.
  • Inoue A; Department of Systems BioMedicine, National Research Institute for Child Health and Development, Setagaya, Tokyo 157-8535, Japan.
  • Seers T; Department of Systems BioMedicine, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Bunkyo, Tokyo 113-8519, Japan.
  • Hato Y; Imperial College London, South Kensington, London SW7 2AZ, United Kingdom.
  • Igarashi A; Department of Breast Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
  • Toyama T; Department of Systems BioMedicine, National Research Institute for Child Health and Development, Setagaya, Tokyo 157-8535, Japan.
  • Taganov KD; Department of Breast Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi 467-8601, Japan.
  • Boldin MP; Division of Biology, California Institute of Technology, Pasadena, CA 91125.
  • Asahara H; Department of Molecular and Cellular Biology, Beckman Research Institute, City of Hope, Duarte, CA 91010.
Proc Natl Acad Sci U S A ; 114(15): 3927-3932, 2017 04 11.
Article em En | MEDLINE | ID: mdl-28356515
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Biblioteca Gênica / MicroRNAs / Receptores de Fator Neurotrófico Derivado de Linhagem de Célula Glial Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Biblioteca Gênica / MicroRNAs / Receptores de Fator Neurotrófico Derivado de Linhagem de Célula Glial Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão