中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2012年
4期
650-652
,共3页
薛万江%冯盈%李鹏%毛勤生%管洪庚%钱海鑫
薛萬江%馮盈%李鵬%毛勤生%管洪庚%錢海鑫
설만강%풍영%리붕%모근생%관홍경%전해흠
肝癌发生%黄曲霉素%Ras相关结构域家族1A%甲基化
肝癌髮生%黃麯黴素%Ras相關結構域傢族1A%甲基化
간암발생%황곡매소%Ras상관결구역가족1A%갑기화
Hepatocarcinogenesis%Aflatoxin B%Ras association domain family 1A gene%Methylation
目的 探讨肝细胞癌(UCC)组织中Ras相关结构域家族1A( RASSF1A)基因甲基化与环境因素的关系.方法 采用甲基化特异性聚合酶链反应检测80例HCC组织中RASSF1A基因甲基化状态,免疫组织化学法检测HCC组织中黄曲霉素B1( AFB1 )-DNA加合物和多环芳烃(PAHs) -DNA加合物的水平,并结合临床资料进行统计分析.结果 RASSF1A基因甲基化率在肝癌组织中(60/80)显著高于癌旁组织(33/80,P<0.01).HCC组织中RASSF1A基因甲基化率在AFB1-DNA加合物阳性组(43/51)高于AFB1-DNA加合物阴性组(17/29,P<0.05);在PAHs-DNA加合物阳性组(39/45)高于PAH-DNA加合物阴性组(21/35,P< 0.05).结论 HCC组织中RASSF1A基因甲基化与环境致癌因素AFBI -DNA加合物、PAHs-DNA加合物水平密切相关.
目的 探討肝細胞癌(UCC)組織中Ras相關結構域傢族1A( RASSF1A)基因甲基化與環境因素的關繫.方法 採用甲基化特異性聚閤酶鏈反應檢測80例HCC組織中RASSF1A基因甲基化狀態,免疫組織化學法檢測HCC組織中黃麯黴素B1( AFB1 )-DNA加閤物和多環芳烴(PAHs) -DNA加閤物的水平,併結閤臨床資料進行統計分析.結果 RASSF1A基因甲基化率在肝癌組織中(60/80)顯著高于癌徬組織(33/80,P<0.01).HCC組織中RASSF1A基因甲基化率在AFB1-DNA加閤物暘性組(43/51)高于AFB1-DNA加閤物陰性組(17/29,P<0.05);在PAHs-DNA加閤物暘性組(39/45)高于PAH-DNA加閤物陰性組(21/35,P< 0.05).結論 HCC組織中RASSF1A基因甲基化與環境緻癌因素AFBI -DNA加閤物、PAHs-DNA加閤物水平密切相關.
목적 탐토간세포암(UCC)조직중Ras상관결구역가족1A( RASSF1A)기인갑기화여배경인소적관계.방법 채용갑기화특이성취합매련반응검측80례HCC조직중RASSF1A기인갑기화상태,면역조직화학법검측HCC조직중황곡매소B1( AFB1 )-DNA가합물화다배방경(PAHs) -DNA가합물적수평,병결합림상자료진행통계분석.결과 RASSF1A기인갑기화솔재간암조직중(60/80)현저고우암방조직(33/80,P<0.01).HCC조직중RASSF1A기인갑기화솔재AFB1-DNA가합물양성조(43/51)고우AFB1-DNA가합물음성조(17/29,P<0.05);재PAHs-DNA가합물양성조(39/45)고우PAH-DNA가합물음성조(21/35,P< 0.05).결론 HCC조직중RASSF1A기인갑기화여배경치암인소AFBI -DNA가합물、PAHs-DNA가합물수평밀절상관.
Objective To investigate the relationship between ras association domain family 1A gene (RASSF1 A) methylation and environmental factors to the hepatocellular carcinoma (HCC).Methods The methylation of RASSF1A was determined by methylation specific polymerase chain reaction (PCR) in 80 genomic DNAs from patients with HCC.Aflatoxin B1 (AFB1)-DNA adducts and polycyclic aromatic hydrocarbons (PAHs)-DNA adducts in tumor tissues were determined by immunohistochemistry.The association between RASSFI A methylation and environmental factors taking into consideration of the clinical biological material was statistically analyzed.Results RASSF1A promoter hypermethylation was detected in 60 of the 80 HCC tissues (75.0%).Of the paired corresponding adjacent tissues from the 80 HCC patients,aberrant methylation was detected in 33 (41.3%).The positive rate for RASSF1A methylation was significantly higher in the HCC tissues than in the paired controls (P <O.O1 ).For AFBI-DNA adducts,the positive rate by methylation specific polymerease chain reaction (MSP) was significantly higher in positive cases (43/51,84.3% ) than in negative cases (17/29,58.6%,P<0.01 ).For PAHs-DNA adduct,the positive rate by MSP was also significantly higher in positive cases ( 39/45,86.7% ) than in negative cses ( 21/35,60.0%,P < O.05 ).Conclusion Statistically significant correlations were observed between RASSF1A methylation and AFB1-DNA adducts or PAHs-DNA adducts in the HCC tissues.