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Genetic changes of p53, K-ras, and microsatellite instability in gallbladder carcinoma in high-incidence areas of Japan and Hungary
Authors:Nagahashi Masayuki  Ajioka Yoichi  Lang Istvan  Szentirmay Zoltan  Kasler Miklos  Nakadaira Hiroto  Yokoyama Naoyuki  Watanabe Gen  Nishikura Ken  Wakai Toshifumi  Shirai Yoshio  Hatakeyama Katsuyoshi  Yamamoto Masaharu
Affiliation:1. Division of Molecular and Diagnostic Pathology,Niigata University Graduate School of Medical and Dental Sciences,Niigata 951-8510,Japan
2. Department of Medical Oncology "B",National Institute of Oncology,Budapest H-1122,Hungary
3. Department of Molecular Pathology,National Institute of Oncology,Budapest H-1122,Hungary
4. Department of Head and Neck Surgery,National Institute of Oncology,Budapest H-l 122,Hungary
5. Department of Nursing,Faculty of Nursing,Social Welfare,and Psychology,Niigata Seiryo University,Niigata 951 -8510,Japan
6. Division of Digestive and General Surgery,Niigata University Graduate School of Medical and Dental Sciences,Niigata 951-8510,Japan
7. Department of Community Preventive Medicine,Niigata University Graduate School of Medical and Dental Sciences,Niigata 951-8510,Japan
Abstract:AIM:To disclose geographic differences in genetic changes involved in gallbladder carcinogenesis between two distinct high-incidence areas of Japan and Hungary. METHODS: We examined 42 cases of gallbladder carcinoma: 22 Japanese and 20 Hungarian cases, p53 mutations at exons 5 to 8 and K-ras mutations at codon 12 were tested by direct sequencing. Microsatellite instability was determined from fluorescent dye-labeled PCR amplifications of five-microsatellite markers (BAT-25, BAT-25, D2S123, D5S346, and D17S250).RESULTS: Mutations of p53 were detected in 11 of 22 Japanese cases and 6 of 18 Hungarian cases (11/22 vs 6/18, P = 0.348). Transition at CpG sites was found in none of 11 Japanese cases and 2 of 6 Hungarian cases; the difference was marginally significant (0/11 vs 2/6,P = 0.110). K-ras mutations were detected in only one of the Hungarian cases. Eight of 19 (42.1%) Japanese cases were MSI-high (presence of novel peaks in more than one of the five loci analyzed), whereas only 1 of 15 (6.7%) Hungarian cases was HSI-high (P = 0.047). CONCLUSION: It appears that the p53 mutations and MSI differ in patients with gallbladder carcinoma between two distinct high-incidence areas. Geographic variation might exist in the process of gallbladder carcinogenesis.
Keywords:Gallbladder  Gallbladder Neoplasms  K-ras  Microsatellite instability  p53
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