• DocumentCode
    2508470
  • Title

    Expression of Fas Ligand Contributes to Formation of Immune Escape in Esophageal Carcinoma

  • Author

    Zheng Shi-ying ; Ge Jing-feng ; Li Hong ; Zhao Jun

  • Author_Institution
    Dept. of Thoracocardiac Surg., Suzhou Univ., Suzhou, China
  • fYear
    2009
  • fDate
    11-13 June 2009
  • Firstpage
    1
  • Lastpage
    5
  • Abstract
    Study the role of Fas ligand (FasL) expression in carcinogenesis and progression of esophageal cancer and molecular mechanisms of relevant immune escape. FasL expression was studied in adjacent epithelial cells, cancer cells and lymphocytes of primary foci, and cancer cells of metastatic foci from 40 cases of esophageal cancer by immunohistochemistry. The relationship between FasL expression in cancer cells and T infiltrating lymphocytes of primary foci was investigated. Positive expression of fas-L genes was detected in 34 HEC cases (85%, 34/40). Positive expression of fas-L genes was detected in 31 T infiltrating lymphocytes of primary foci (82.5%, 31/40). Positive expression of fas-L genes was detected in 17 cancer cells of metastases (100%, 17/17). Up-regulated expression of FasL a in cancer cells of primary foci play an important role in esophageal carcinogenesis. As an effective marker to reveal the biological behaviors, FasL is implicated in metastasis of esophageal cancer by inducing apoptosis of infiltrating lymphocytes.
  • Keywords
    biological organs; biomembranes; cancer; cellular biophysics; genetics; molecular biophysics; proteins; tumours; T infiltrating lymphocyte; cancer cell; epithelial cell; esophageal carcinoma; fas-ligand gene expression; immune escape formation; immunohistochemistry; induced apoptosis; molecular mechanism; Birth disorders; Cancer; Esophagus; Hospitals; Immune system; Lymph nodes; Metastasis; Neoplasms; Pathology; Testing;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
  • Conference_Location
    Beijing
  • Print_ISBN
    978-1-4244-2901-1
  • Electronic_ISBN
    978-1-4244-2902-8
  • Type

    conf

  • DOI
    10.1109/ICBBE.2009.5162835
  • Filename
    5162835