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. Carbonic anhydrase ix promotes human cervical cancer cell motility by regulating pfkfb4 expression
 
  • Details
Options

Carbonic anhydrase ix promotes human cervical cancer cell motility by regulating pfkfb4 expression

Journal
Cancers
Date Issued
2021-03-01
Author(s)
YI-HSIEN HSIEH  
PEI-NI CHEN  
SHUN-FA YANG  
DOI
10.3390/cancers13051174
URI
https://www.scopus.com/pages/publications/85102123719
https://scholars.csmu.edu.tw/handle/123456789/28282
Abstract
Carbonic anhydrase IX (CAIX) is a hypoxia‐induced protein that is highly expressed in numerous human cancers. However, the molecular mechanisms involved in CAIX and human cervical cancer metastasis remain poorly understood. In this study, CAIX overexpression in SiHa cells increased cell migration and epithelial‐to‐mesenchymal transition (EMT). Silencing CAIX in the Caski cell line decreased the motility of cells and EMT. Furthermore, the RNA‐sequencing analysis identified a target gene, bifunctional 6‐phosphofructo‐2‐kinase/fructose‐2,6‐bisphosphatases (PFKFB4), which is influenced by CAIX overexpression and knockdown. A positive correlation was found between CAIX expression and PFKFB4 levels in the cervical cancer of the TCGA database. Mechanistically, CAIX overexpression activated the phosphorylation of extracellular signal‐regulated kinases (ERKs) to induce EMT and promote cell migration. In clinical results, human cervical cancer patients with CAIXhigh /PFKFB4high expression in the late stage had higher rates of lymph node metastasis and the shortest survival time. Our study found that CAIX overexpression increases PFKFB4 expression and EMT, pro-moting cervical cancer cell migration. CAIX could contribute to cervical cancer cell metastasis and its inhibition could be a cervical cancer treatment strategy.
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