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作 者:梁晓秋[1] 苏琦[1] 杨和平 朱建思 周建国 李一琴
机构地区:[1]衡阳医学院肿瘤研究所
出 处:《中国肿瘤临床》1999年第5期352-354,共3页Chinese Journal of Clinical Oncology
基 金:湖南省卫生厅科研基金
摘 要:目的:研究胃癌组织中GST-π的表达与其基因甲基化状态的关系。方法:应用S-P法检测116例胃癌和53例胃癌前病变的GST-π表达和限制性内切酶及PCR、Southern印迹方法检测14例胃癌及其相应正常胃粘膜GST-πDNA5′端调控区CCGG特定位点的甲基化水平。结果:GST-π阳性率,正常胃粘膜10%(4/39),胃癌77%(89/116),肠上皮化生76%(19/25),不典型增生89%(25/28)。GST-π在胃癌及癌前病变中的表达较正常胃粘膜增高(P<001)。胃癌组织中GST-π基因较正常胃粘膜呈现高度去甲基化(P<001),胃癌GST-π基因5′端调控区低甲基化与其GST-π表达增加呈相关性(P<005)。结论:GST-π在胃癌及癌前病变中的表达与胃癌的发生发展密切相关,GST-π可作为胃癌的肿瘤相关抗原;GST-π基因5′端调控区低甲基化可能是GST-π高表达的分子机理。Objective: To study the relationship between the expression of GST- and methylation status of GST- gene in gastric cancers Methods: The GST- was detected in 116 human gastric cancers and 53 precancerous lesions with S-P immunohistochemical method using GST- monoclonal antibody The methylation status of the 5end regulatory sequence CCGG site of GST- gene was also investigated by means of restriction endonuclease analysis, PCR and Southern blotting methods in 14 human gastric cancers and normal gastric mucosa Results: The positive rate of GST- in normal gastric mucosa, intestinal metaplasia, atypical hyperplasia and gastric cancer were 10%(4/39), 76%(19/25), 89%(25/28), 77%(89/116) respectively The positive rate in gastric cancer and precancerous lesions were markedly higher than that of the normal gastric mucosa (P< 001) As compared with that of the normal gastric mucosa, the GST- DNA of gastric cancer was markedly hypomethylated (P< 001) A close correlation existed between overexpression of GST- DNA methylationand hypomethylation of GST- DNA in gastric cancer (P< 005) Conclusion: GST- is probably involved in the carcinogenesis and development of gastric cancer, and is a tumor associated antigen of gastric cancer Hypomethylation of GST- gene might be a molecular factor responsible for overexpression of GST-
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