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. Potential impact of omentin-1 genetic variants with the clinical features and progression of buccal mucosa cancer
 
  • Details
Options

Potential impact of omentin-1 genetic variants with the clinical features and progression of buccal mucosa cancer

Journal
International Journal of Medical Sciences
Date Issued
2025-01-01
Author(s)
CHIAO-WEN LIN  
SHUN-FA YANG  
DOI
10.7150/ijms.117708
URI
https://www.scopus.com/pages/publications/105016873859
https://scholars.csmu.edu.tw/handle/123456789/24188
Abstract
Oral cancer is the fourth most prevalent cancer among Taiwanese men and the ninth most general cancer among men globally. Omentin-1, an adipokine, has been shown to play a protective role by reducing proinflammatory cytokine secretion. The relationships between carcinogenic lifestyle factors, OMNT1 polymorphisms, and oral squamous cell carcinoma (OSCC) remain unclear. We investigated the impact of clinicopathological features and four OMNT1 gene variants on oral cancer risk in 406 Taiwanese male patients with the condition. Compared with the TT genotype, the TA+AA genotypes of SNP rs2274907 were linked with an increased risk of advanced clinical stage (III+IV). In patients with OSCC who consumed betel quid and cigarette smoke, SNP rs2274907 was associated with a higher risk of advanced clinical stage (III+IV) and lymph node metastasis. Interestingly, the wild-type TT homozygous genotype was associated with significantly higher OMNT1 expression levels compared to the AA allele of variant rs2274907. Additionally, OMNT1 mRNA levels were lower in oral cancer tissues compared to normal tissues, indicating that omentin-1 acts as a negative regulator of oral cancer.
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