Repository logo
  • English
  • äø­ę–‡
  • 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
  • äø­ę–‡
  • Log In
    New user? Click here to register.Have you forgotten your password?
  1. Home
  2. Chung Shan Medical University
  3. Pureå­øč”“äŗŗę‰åŗ«č½‰å…„
  4. PKCα expression regulated by Elk-1 and MZF-1 in human HCC cells
 
  • Details
Options

PKCα expression regulated by Elk-1 and MZF-1 in human HCC cells

Journal
Biochemical and Biophysical Research Communications
Date Issued
2006-01-06
Author(s)
YI-HSIEN HSIEH  
DOI
10.1016/j.bbrc.2005.11.015
URI
https://www.scopus.com/pages/publications/28144454650
https://scholars.csmu.edu.tw/handle/123456789/28224
Abstract
Our previous study found that PKCα was highly expressed in the poor-differentiated human HCC cells and associated with cell migration and invasion. In this study, we further investigated the gene regulation of this enzyme. We showed that PKCα expression enhancement in the poor-differentiated human HCC cells was found neither by DNA amplification nor by increasing mRNA stability using differential PCR and mRNA decay assays. After screening seven transcription factors in the putative cis-acting regulatory elements of human PKCα promoters, only Elk-1 and MZF-1 antisense oligonucleotide showed a significant reduction in the PKCα mRNA level. They also reduced cell proliferation, cell migratory and invasive capabilities, and DNA binding activities in the PKCα promoter region. Over-expression assay confirmed that the PKCα expression may be modulated by these two factors at the transcriptional level. Therefore, these results may provide a novel mechanism for PKCα expression regulation in human HCC cells.
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