Functional Defect of the Fas Mutants Detected in Gastric Cancers.
10.5230/jkgca.2003.3.4.186
- Author:
Won Sang PARK
1
;
Young Gu CHO
;
Chang Jae KIM
;
Cho Hyun PARK
;
Young Sil KIM
;
Su Young KIM
;
Suk Woo NAM
;
Sug Hyung LEE
;
Nam Jin YOO
;
Jung Young LEE
Author Information
1. Department of Pathology, College of Medicine, The Catholic University of Korea, Seoul 137-701, Korea. stingray@catholic.ac.kr
- Publication Type:Original Article
- Keywords:
Apoptosis;
Cell death;
Fas;
Death receptor;
Mutation
- MeSH:
Antigens, CD95;
Apoptosis;
Cell Death;
Cell Proliferation;
Clone Cells;
Cytoplasm;
DNA, Complementary;
HEK293 Cells;
Liver;
Microscopy;
Mutagenesis;
Stomach Neoplasms*;
Transfection;
United Nations
- From:Journal of the Korean Gastric Cancer Association
2003;3(4):186-190
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: The balance between cell proliferation and apoptosis is crucial for homeostatic maintenance in a cell population. Decreased apoptosis or uncontrolled proliferation can lead to cancer. The Fas receptor signal through a cytoplasmic death domain is very important in the apoptotic pathway. To identify the effect of the death domain of the Fas gene in the development and/or progression of gastric cancer, we examined the apoptotic potential of five known Fas mutants detected in gastric cancers. MATENRIALS AND METHODS: A wild-type Fas gene was cloned with cDNA from normal liver tissue and full length Fas was sequenced. Mutants of the gene were generated with site- directed mutagenesis by using the wild-type gene and specific primers. Wild- and mutant-type genes were transfected to HEK293 cells. Forty-eight hours after transfection the cells were stained with DAPI and cell death was counted under fluorescent microscopy. RESULTS: In wild-type Fas-transfected cells, the percentage of apoptotic cells was 85.9+/-3.6%, and significant cell death and classic morphologic signs of apoptosis were observed. However, the percentages of apoptotic cells transfected with N239D, E240G, D244V, and R263H of tumor-derived mutant Fas were 29.5+/-2.08%, 28.5+/-3.34%, 25.225+/-2.06%, and 36.625+/-4.49%, respectively. CONCLUSION: These results suggest that inactivation of Fas caused by mutations in the death domain of the Fas gene may be one of the possible escape mechanisms against Fas-mediated apoptosis and that inactivating mutation of the Fas may contribute to the development or progression of gastric cancers.
