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GSE1 negative regulation by miR-489-5p promotes breast cancer cell proliferation and invasion.
Chai, Peng; Tian, Jingzhong; Zhao, Deyin; Zhang, Hongyan; Cui, Jian; Ding, Keshuo; Liu, Bin.
Afiliação
  • Chai P; Department of General Surgery, The People's Hospital of Bozhou, Bozhou 236800, PR China. Electronic address: chaiyisheng0508@sina.com.
  • Tian J; Department of General Surgery, The People's Hospital of Bozhou, Bozhou 236800, PR China.
  • Zhao D; Dept of General Surgery, The Hospital of Suzhou, Suzhou 234000, PR China.
  • Zhang H; Department of General Surgery, The People's Hospital of Bozhou, Bozhou 236800, PR China.
  • Cui J; Department of General Surgery, The People's Hospital of Bozhou, Bozhou 236800, PR China.
  • Ding K; Department of Pathology, Anhui Medical University, Hefei 230022, PR China.
  • Liu B; Dept of Vascular Surgery, The First Affiliated Hospital, Anhui Medical University, Hefei 230022, PR China. Electronic address: 13399519008@163.com.
Biochem Biophys Res Commun ; 471(1): 123-8, 2016 Feb 26.
Article em En | MEDLINE | ID: mdl-26828271
Gse1 coiled-coil protein (GSE1), also known as KIAA0182, is a proline rich protein. However, the function of GSE1 is largely unknown. In this study, we reported that GSE1 is overexpression in breast cancer and silencing of GSE1 significantly suppressed breast cancer cells proliferation, migration and invasion. Furthermore, GSE1 was identified as a direct target of miR-489-5p, which is significantly reduced in breast cancer tissues. In addition, forced expression of miR-489-5p suppressed breast cancer cells proliferation, migration and invasion. Moreover, depletion of GSE1 by siRNAs significantly abrogated the enhanced proliferation, migration and invasion of breast cancer cells consequent to miR-489-5p depletion. Taken together, these findings suggest that GSE1 may function as a novel oncogene in breast cancer and it can be regulated by miR-489-5p.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Movimento Celular / MicroRNAs / Proliferação de Células / Proteínas de Neoplasias Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Movimento Celular / MicroRNAs / Proliferação de Células / Proteínas de Neoplasias Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Biochem Biophys Res Commun Ano de publicação: 2016 Tipo de documento: Article