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作 者:刘振芳[1] 刘宏斌[2] 韩晓鹏[2] 朱万坤[2] 苏林[2] 李文慧[2]
机构地区:[1]兰州大学第二临床医学院,甘肃兰州730050 [2]兰州军区兰州总医院普外科,甘肃兰州730050
出 处:《现代肿瘤医学》2010年第9期1785-1788,共4页Journal of Modern Oncology
基 金:全军医学科学技术研究"十一五"计划课题项目(编号:06MA082)
摘 要:目的:运用细胞学及实时荧光定量RT-PCR方法对胃癌术中腹腔冲洗液进行检测,以探讨对预测胃癌腹膜微转移的意义。方法:胃癌50例和胃良性病变10例,收集患者术中腹腔冲洗液,用实时荧光定量RT-PCR方法测定腹腔冲洗液中游离细胞的CK20mRNA、COX-2 mRNA表达,同时作冲洗液细胞学检测(PLC)。结果:50例胃癌患者腹腔冲洗液中CK20mRNA阳性表达为62.0%(31/50);COX-2 mRNA阳性表达率60.0%(30/50),CK20mRNA、COX-2 mRNA联合检测阳性率为68.0%(34/50),皆高于腹腔冲洗液细胞学28.2%(11/50),CK20mRNA、COX-2 mRNA的阳性率与肿瘤分期、浸润深度、淋巴结转移、浆膜侵犯程度呈正相关。结论:CK20mRNA、COX-2 mRNA实时荧光定量RT-PCR方法检测腹腔微量游离癌细胞较PLC有更高的灵敏度,是一种检测胃癌腹膜微转移的有效方法。Objective:To detect the free cancer cells in the peritoneal washes and to explore their signifcances in the prediction of peritoneal metastasis of gastric cancer. Methods: The peritoneal washes were collected from 50 patients with gastric cancer and 5 with benign gastric disease. Peritoneal lavage cytology was performed for the washes, and CK20mRNA,COX-2 mRNA of free cancer cells was detected by real-time fluorescence quantitative reverse transcription polymerase chain reaction(fqRT-PCR). Results: CK20mRNA,COX-2 mRNA positive rates of free cancer cells in peritoneal washes were 62.0%(31/50) and 60.0%(30/30), respectively, which were both higher than that of cytological examination 28.2% (11/50). The TNM staging, depth of invasion, lymph node metastasis, serosal involvement were correlated with the positive rate of CK20mRNA,COX-2 mRNA. Conclusion: CK20mRNA,COX-2mRNA detected by real-time fluorescence quantitative reverse transcription polymerase chain reaction is more sensitive for peritoneal micrometastasis of gastric cancer.
关 键 词:胃癌 微转移 实时荧光定量RT-PCR 肿瘤标志物 PLC
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