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Association of Fas-670 gene polymorphism with inflammatory bowel disease in Chinese patients 被引量:15

Association of Fas-670 gene polymorphism with inflammatory bowel disease in Chinese patients
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摘要 AIM: Recent studies suggest that Fas-mediated apoptosis is involved in the pathogenesis of inflammatory bowel disease (IBD). It has been hypothesized that either increased apoptosis of intestinal epithelium or decreased apoptosis of lamina propria lymphocytes may induce inflammation of gut. The aim of this study was to determine whether the Fas gene promoter polymorphism at position-670 was associated with IBD in Chinese patients.METHODS: Fifty unrelated Chinese patients with IBD (38patients with ulcerative colitis and 12 with Crohn's disease)and 124 healthy controls were genotyped for the Fas-670polymorphism by PCR-restriction fragment length polymorphism method. The PCR product was digested by Mva I restriction enzyme.RESULTS: Distribution of the Fas-670 gene polymorphism was 33% for the AA genotype, 52% for the AG genotype and 15% for the GG genotype in 124 healthy subjects. In patients with IBD, 30% was for the AA genotype, 42% for the AG genotype and 28% for the GG genotype respectively. However, there was no significant difference in the genotype (P= 0.1498), allele frequencies (P= 0.3198)and carriage frequencies (P = 0.4133) between healthy controls and IBD patients. Furthermore, we did not find any difference between the left-sided colitis and total colitis (P = 0.8242).CONCLUSION: Fas-670 polymorphism is not associated with IBD in Chinese patients. AIM: Recent studies suggest that Fas-mediated apoptosis is involved in the pathogenesis of inflammatory bowel disease (IBD). It has been hypothesized that either increased apoptosis of intestinal epithelium or decreased apoptosis of lamina propria lymphocytes may induce inflammation of' gut. The aim of this study was to determine whether the Fas gene promoter polymorphism at position-670 was associated with IBD in Chinese patients. METHODS: Fifty unrelated Chinese patients with IBD (38 patients with ulcerative colitis and 12 with Crohn's disease) and 124 healthy controls were genotyped for the Fas-670 polymorphism by PCR-restriction fragment length polymorphism method. The PCR product was digested by Mva I restriction enzyme. RESULTS: Distribution of the Fas-670 gene polymorphism was 33% for the AA genotype, 52% for the AG genotype and 15% for the GG genotype in 124 healthy subjects. In patients with IBD, 30% was for the AA genotype, 42% for the AG genotype and 28% for the GG genotype respectively. However, there was no significant difference in the genotype (P= 0.1498), allele frequencies (P= 0.3198) and carriage frequencies (P = 0.4133) between healthy controls and IBD patients. Furthermore, we did not find any difference between the left-sided colitis and total colitis (P = 0.8242). CONCLUSION: Fas-670 polymorphism is not associated with IBD in Chinese patients.
出处 《World Journal of Gastroenterology》 SCIE CAS CSCD 2005年第3期415-417,共3页 世界胃肠病学杂志(英文版)
基金 Supported by a Grant From National Natural Science Foundation of China, No.30070350
关键词 Inflammatory bowel disease Fas-670 gene APOPTOSIS POLYMORPHISM Fas-670基因 基因多态性 肠炎 中国 消化系统
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  • 1Nagata S, Golstein P. The Fas death factor. Science 1995; 267:1449-1456.
  • 2Bu P, Keshavarzian A, Stone DD, Liu J, Le PT, Fisher S, Qiao L.Apoptosis: one of the mechanisms that maintains unresponsiveness of the intestinal mucosal immune system. J Immunol 2001; 166:6399-6403.
  • 3Boirivant M, Pica R, DeMaria R, Testi R, Pallone F, Strober W.Stimulated human lamina propria T ceils manifest enhanced Fas-mediated apoptosis. J Clin Invest 1996; 98:2616-2622.
  • 4Strater J, Wellisch I, Riedl S, Walczak H, Koretz K, Tandara A,Krammer PH, Moiler P. CD95 (APO-1/Fas)-mediated apoptosis in colon epithelial ceils: A possible role in ulcerative colitis. Gastroenterology 1997; 113:160-167.
  • 5Ueyama H, Kiyohara T, Sawada N, Isozaki K, Kitamura S,Kondo S, Miyagawa J, Kanayama S, Shinomura Y, Ishikawa H, Ohtani T, Nezu R, Nagata S, Matsuzawa Y. High Fas ligand expression on lymphocytes in lesions of ulcerative colitis. Gut 1998; 43:48-55.
  • 6Iwamoto M, Koji T, Makiyama K, Kobayashi N, Nakane PK.Apoptosis of crypt epithelial cells in ulcerative colitis. J Pathol 1996; 180:152-159.
  • 7Levine AD, Fiocchi C. Regulation of life and death in lamina propria T cells. Semin Immunol 2001; 13:195-199.
  • 8Suzuki A, Sugimura K, Ohtsuka K, Hasegawa K, Suzuki K,Ishizuka K, Mochizuki T, Honma T, Narisawa R, Asakura H.Fas/Fas ligand expression and characteristics of primed CD45RO+T cells in the inflamed mucosa of ulcerative colitis.Scand J Gastroenterol 2000; 35:1278-1283.
  • 9Inazawa J, Itoh N, Abe T, Nagata S. Assignment of the human Fas antigen gene (Fas) to 10q24.1. Genomics 1992; 14:821-822.
  • 10Huang QR, Morris D, Manolios N. Identification and characterization of polymorphisms in the promoter region of the human Apo-1/Fas (CD95) gene. Mol Immunol 1997; 34:577-582.

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