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MicroRNA-24 increases hepatocellular carcinoma cell metastasis and invasion by targeting p53: miR-24 targeted p53.
Chen, Li; Luo, Liang; Chen, Wei; Xu, Hong-Xu; Chen, Fan; Chen, Lian-Zhou; Zeng, Wen-Tao; Chen, Jing-Song; Huang, Xiao-Hui.
Afiliação
  • Chen L; Department of General Surgical Laboratory, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510080, China; Emergency Department, Chinese PLA General Hospital, Beijing, China.
  • Luo L; Department of Medical Intensive Care Unit, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
  • Chen W; Department of Pancreato-Billary, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
  • Xu HX; Departments of Laboratory, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
  • Chen F; Department of General Surgical Laboratory, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510080, China.
  • Chen LZ; Department of General Surgical Laboratory, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510080, China.
  • Zeng WT; Department of General Surgical Laboratory, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510080, China.
  • Chen JS; Department of Gastrointestinal Surgery, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China. Electronic address: hychenjs@126.com.
  • Huang XH; Department of General Surgical Laboratory, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510080, China. Electronic address: hxiaohui2006@126.com.
Biomed Pharmacother ; 84: 1113-1118, 2016 Dec.
Article em En | MEDLINE | ID: mdl-27780140
MicroRNA-24 (miR-24), a member of the miRNA family, functions as an oncogene in various types of human cancer. However, the underlying mechanisms of miR-24 involvement in the development and progression of hepatocellular carcinoma (HCC) remain poorly understood. The present study revealed that miRNA-24 down-regulates p53 through binding to the 3'-UTR of p53 mRNA based on a luciferase reporter assay, and that the expression level of miR-24 could affect the invasion of HCC lines via p53. Down-regulation of p53 significantly attenuated the inhibitory effects of miR-24 knockdown on the invasion of HCC cells, suggesting that miR-24 could be a potential target for HCC treatment. Moreover, our results revealed that miR-24 expression was significantly increased in HCC metastatic tumor tissues compared with matched non-metastatic tumor tissues, and that the up-regulation of miR-24 was significantly associated with down-regulation of p53 in the HCC tissues. In conclusion, this study demonstrates that miR-24 functions as an oncogene in HCC, at least partly by promoting cell invasion through down-regulation of p53. Therefore, miR-24 may be a potential therapeutic target for treatment of HCC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação Neoplásica da Expressão Gênica / Movimento Celular / Proteína Supressora de Tumor p53 / Carcinoma Hepatocelular / MicroRNAs / Neoplasias Hepáticas Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação Neoplásica da Expressão Gênica / Movimento Celular / Proteína Supressora de Tumor p53 / Carcinoma Hepatocelular / MicroRNAs / Neoplasias Hepáticas Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article