Your browser doesn't support javascript.
loading
Downregulation of cyclin-dependent kinase 8 by microRNA-148a suppresses proliferation and invasiveness of papillary thyroid carcinomas.
Han, Chun; Zheng, Weihui; Ge, Minghua; Wang, Kejing; Xiang, Yangfeng; Wang, Peng.
Afiliação
  • Han C; Department of Head & Neck Surgery, Zhejiang Cancer HospitalHangzhou 310022, China.
  • Zheng W; Department of Head & Neck Surgery, Zhejiang Cancer HospitalHangzhou 310022, China.
  • Ge M; Department of Head & Neck Surgery, Zhejiang Cancer HospitalHangzhou 310022, China.
  • Wang K; Department of Head & Neck Surgery, Zhejiang Cancer HospitalHangzhou 310022, China.
  • Xiang Y; Department of Head & Neck Surgery, Zhejiang Cancer HospitalHangzhou 310022, China.
  • Wang P; Department of Head & Neck Surgery, Zhejiang Cancer HospitalHangzhou 310022, China.
Am J Cancer Res ; 7(10): 2081-2090, 2017.
Article em En | MEDLINE | ID: mdl-29119056
ABSTRACT
MicroRNAs (miRNAs) are important gene regulators that play key roles in tumor genesis. In this study, we investigate the role of miR-148a in the development of papillary thyroid cancer (PTC). Data from the cancer genome atlas (TCGA) indicate that miR-148a is downregulated in PTC tissues; we also find that miR-148a is downregulated in tissue samples from PTC patients and PTC cell lines. Overexpression of miR-148a significantly suppresses PTC cell proliferation, migration and invasiveness in vitro, and inhibits tumor growth in vivo as well. We have identified the cyclin-dependent kinase 8 (CDK8) gene as a direct target of miR-148a using the online software packages TargetScan and miRanda. Overexpression of miR-148a significantly represses CDK8 expression by directly targeting the 3'-untranslated region (3'-UTR) of the CDK8 gene in PTC tissues and cell lines; overexpression of CDK8 reverses the inhibitory effects of miR-148a on PTC cell growth, migration and invasiveness. Taken together, our results indicate that miR-148a functions as a tumor suppressor in PTC by repressing CDK8 expression.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article