Repository logo
  • English
  • 中文
  • Log In
    New user? Click here to register.Have you forgotten your password?
Repository logo
    Communities & Collections
    Research Outputs
    Fundings & Projects
    People
    Organizations
    Statistics
  • English
  • 中文
  • Log In
    New user? Click here to register.Have you forgotten your password?
  1. Home
  2. Chung Shan Medical University
  3. Pure學術人才庫轉入
  4. The role of HPV-18 E6 and E7 in a human basal cell carcinoma cell line
 
  • Details
Options

The role of HPV-18 E6 and E7 in a human basal cell carcinoma cell line

Journal
Life Science Journal
Date Issued
2013-01-01
Author(s)
WEN-JUN WU  
YU-PING HSIAO  
URI
https://www.scopus.com/pages/publications/84888173319
https://scholars.csmu.edu.tw/handle/123456789/26665
Abstract
Basal cell carcinoma (BCC) is the most common skin cancer, but the pathogenic role of human papillomavirus (HPVs) in BCC is not still completely understood. In this study, we investigate the involvement of the integrated HPV-18 E6 and E7 in proliferation and senescence in a human BCC cell line. We had demonstrated HPV-18 E6 and E7 proteins in the BCC cell line. The inducible shRNA system was applied to suppress E6 and E7 expression and the cells were selected for further investigation. The effect of E6/E7 inhibition were analyzed by MTT, clonogenic assay and senescence-associated β-galactosidase staining. Our data show that repression of E6 and E7 in BCC cells result in proliferation inhibition and cellular senescence. Combined with the results of previous inducible shRNA inhibition system, we showed that HPV E6 downregulates p53 and E7 downregulates Rb proteins. Furthermore, integrated E6/E7 genes of HPV-18 upregulate the pro-inflammatory cytokines IL-6 and IL-8. These results suggest that HPV-18 involved in the tumorigenesis of BCC cell line.
Type
journal article
Make it your own

DSpace-CRIS can be extensively configured to meet your needs. Decide which information need to be collected and available with fine-grained security. Start updating the theme to match your Institution's web identity.

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science

  • Cookie settings
  • Privacy policy
  • End User Agreement
  • Send Feedback