Geographic characterization of hepatitis virus infections, genotyping of hepatitis B virus, and p53 mutation in hepatocellular carcinoma analyzed by in situ detection of viral genomes from carcinoma tissues: Comparison among six different countries

被引:0
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作者
Ding, X
Park, YN
Taltavull, TC
Thung, SN
Jin, XM
Jin, Y
Trung, NS
Edamoto, Y
Sata, T
Abe, K
机构
[1] Natl Inst Infect Dis, Dept Pathol, Shinjuku Ku, Tokyo 1628640, Japan
[2] Nagoya Univ, Grad Sch Med, Dept Pathol, Aichi 4668550, Japan
[3] Int Med Ctr Japan, Div Surg, Tokyo 1628655, Japan
[4] Yonsei Univ, Coll Med, Dept Pathol, Seoul, South Korea
[5] Bellvitge Hosp, Liver & Kidney Transplant Unit, Barcelona, Spain
[6] CUNY, Mt Sinai Med Ctr, Dept Pathol, New York, NY USA
[7] Harbin Med Univ, Dept Pathol, Harbin, Peoples R China
[8] Univ Med & Pharm, Dept Pathol, Ho Chi Minh City, Vietnam
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中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
We investigated the relationship of infection with hepatitis B virus (HBV) and hepatitis C virus (HCV) to p53 mutation in hepatocellular carcinomas (HCC) from six countries, including Japan, China, Korea, Vietnam, Spain, and the Unites States. For this purpose, we used formalin-fixed, paraffin-embedded liver tissues obtained from 449 patients with HCC to detect the viral and p53 genes by polymerase chain reaction (PCR). HBV was the most prevalent in Korea (69.1%), China (66.1%), Vietnam (60.5%), and Spain (38.6%). In contrast, HCV was the most prevalent in Japan (59.8%) and in the United States (41.5%). Type C of HBV was the most common genotype (78.6%) encountered in HCC in these countries. Importantly, among 125 intrahepatic HBV DNA-positive patients, 44 (35.2%) were serologically negative for HBsAg (occult hepatitis B). Based on PCR, immunohistochemical, serological, and clinical findings, 4.8% of HCC patients were diagnosed with non-B, non-C. A point mutation at exon 7 of p53 was detected in 20 of the 239 HCC samples examined, including those from 9 Chinese, 5 American, 2 Japanese, 2 Korean, and 2 Spanish patients, respectively. Interestingly, a point mutation with an amino acid substitution at codon 251 (Ile-->Asn) was detected frequently in 11 of 20 (55%) cases. A specific mutation induced by aflatoxin B, at codon 249 was seen in two patients, both Chinese. Our results suggest that genotype C of HBV may play an important role in hepatocarcinogenesis in different geographic regions, and that in situ detection of HBV genomes could be important for clarifying the agent(s) of unknown etiology related to HCC.
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页码:12 / 18
页数:7
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