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MicroRNA-219-5p exerts tumor suppressor function by targeting ROBO1 in glioblastoma.
Jiang, Yongmei; Yin, Lin; Jing, Huirong; Zhang, Hui.
Afiliação
  • Jiang Y; Department of Neurology, Second Affiliated Hospital, Dalian Medical University, No. 467 Zhongshan Road, Dalian, Liaoning, 116027, China. zhuxufifa2007@163.com.
  • Yin L; Department of Neurology, Second Affiliated Hospital, Dalian Medical University, No. 467 Zhongshan Road, Dalian, Liaoning, 116027, China. Lin_yin1@163.com.
  • Jing H; Department of Neurology, Second Affiliated Hospital, Dalian Medical University, No. 467 Zhongshan Road, Dalian, Liaoning, 116027, China. Huirong_jing@163.com.
  • Zhang H; Department of Neurology, Second Affiliated Hospital, Dalian Medical University, No. 467 Zhongshan Road, Dalian, Liaoning, 116027, China. Hui_zhang2014@163.com.
Tumour Biol ; 36(11): 8943-51, 2015 Nov.
Article em En | MEDLINE | ID: mdl-26081620
ABSTRACT
Previous studies have shown that miR-219-5p is dysregulated and exerts tumor-suppressive effects in cancer development and progression. However, the molecular function and mechanism of miR-219-5p in glioblastoma growth and invasion are still unclear. In the present study, we show that miR-219-5p was downregulated in a panel of glioma tissues with different grades and in all the human glioma cell lines examined. Ectopic expression of miR-219-5p inhibited proliferation and invasion and induced apoptosis in vitro, and xenograft formation in vivo. ROBO1 was found to be a direct target of miR-219-5p, and when overexpressed in miR-219-5p-expressing glioma cells, was able to restore proliferative and invasive ability. Finally, in vivo investigation confirmed that miR-219-5p was a tumor suppressor that regulated ROBO1 expression. Taken together, these studies demonstrate that miR-219-5p inhibited cancer cell growth and invasion by direct targeting ROBO1, implicating miR-219-5p as an attractive candidate for cancer therapy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores Imunológicos / Transformação Celular Neoplásica / Glioblastoma / MicroRNAs / Proteínas do Tecido Nervoso Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores Imunológicos / Transformação Celular Neoplásica / Glioblastoma / MicroRNAs / Proteínas do Tecido Nervoso Idioma: En Ano de publicação: 2015 Tipo de documento: Article