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MicroRNA-766 targeting regulation of SOX6 expression promoted cell proliferation of human colorectal cancer.
Li, Yong-Chao; Li, Chang-Feng; Chen, Li-Bo; Li, Dan-Dan; Yang, Lei; Jin, Jing-Peng; Zhang, Bin.
Afiliação
  • Li YC; Department of Gastrointestinal Surgery, China-Japan Union Hospital of Jilin University, Changchun, People's Republic of China.
  • Li CF; Department of Endoscopy Center, China-Japan Union Hospital of Jilin University, Changchun, People's Republic of China.
  • Chen LB; Department of Endoscopy Center, China-Japan Union Hospital of Jilin University, Changchun, People's Republic of China.
  • Li DD; Department of Endoscopy Center, China-Japan Union Hospital of Jilin University, Changchun, People's Republic of China.
  • Yang L; Department of Endoscopy Center, China-Japan Union Hospital of Jilin University, Changchun, People's Republic of China.
  • Jin JP; Department of Endoscopy Center, China-Japan Union Hospital of Jilin University, Changchun, People's Republic of China.
  • Zhang B; Department of Endoscopy Center, China-Japan Union Hospital of Jilin University, Changchun, People's Republic of China.
Onco Targets Ther ; 8: 2981-8, 2015.
Article em En | MEDLINE | ID: mdl-26543373
ABSTRACT
MicroRNAs (miRNAs) have emerged as important regulators of cancer-cell biological processes. Previous studies have shown that miR-766 plays an important role in a variety of biological processes in various human cancers. However, the underlying mechanism of miR-766 in colorectal cancer (CRC) cells remains unclear. In this study, we investigated miR-766's role in CRC cell proliferation. Polymerase chain reaction results showed that miR-766 expression was significantly upregulated in CRC tissues and cells. Ectopic expression of miR-766 promoted cell growth and anchorage-independent growth in CRC cells. Bioinformatic analysis predicted SOX6, a potential target of miR-766, acting as a tumor suppressor. Luciferase reporter assay results demonstrated that miR-766 directly bound to the 3'-untranslated region of SOX6. Overexpression of miR-766 suppressed SOX6 expression, resulting in the downregulation of p21 and upregulation of cyclin D1. In a further experiment, SOX6-silenced SW480 cells transfected with miR-766 promoted cell growth, suggesting that downregulation of SOX6 was required for miR-766-induced CRC cell proliferation. Taken together, these results suggested that miR-766 represents an onco-miRNA and participates in the development of CRC by modulating SOX6 expression.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article