巢式聚合酶链反应技术检测肝癌微转移灶中Gpc3和Afp mRNA的表达。

J. Luo, K. Yang, Y. Wen
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引用次数: 7

摘要

肝癌在中国的发病率已经逐渐上升到较高水平,并且肿瘤的转移是通过多种途径发生的。胎儿α蛋白(AFP)是肝癌微转移的主要生物标志物。最近的一项研究表明,glypican-3 (GPC3)在肝癌细胞中含量丰富,具有良好的特异性,可用于判断恶性细胞的存在。巢式聚合酶链反应(PCR)技术在实验灵敏度上具有优越性。本研究利用肝癌大鼠模型,采用巢式PCR检测Gpc3和Afp mRNA,以确定其与肝癌微转移的关系。目的是为临床检查提供实验依据。我们将雄性Sprague-Dawley大鼠随机分为假手术组和实验组。实验组建立二乙基亚硝胺致肝癌模型,假手术组给予等量生理盐水。采用巢式PCR检测Gpc3和Afp mRNA。进行分析以确定统计学意义。与假手术组比较,实验组Gpc3、Afp mRNA的出现率显著高于假手术组(P < 0.05)。与联合检测肝癌细胞总阳性率比较,实验组4个亚组Gpc3、Afp mRNA的出现率均显著升高(P < 0.05)。巢式PCR检测肝癌微转移灶中Gpc3和Afp mRNA的灵敏度显著提高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nested polymerase chain reaction technique for the detection of Gpc3 and Afp mRNA in liver cancer micrometastases.
The incidence of liver cancer has gradually risen to a high level in China, and tumor metastasis occurs via multiple pathways. Alpha fetal protein (AFP) is the main biomarker of liver cancer micrometastases. A recent study showed that glypican-3 (GPC3), which is abundant in hepatoma cells, has promising specificity and could be used to determine the presence of malignant cells. The nested polymerase chain reaction (PCR) technique is superior in experimental sensitivity. Using rat models of liver cancer in the current study, we utilized nested PCR to detect Gpc3 and Afp mRNA to determine their relationship with liver cancer micrometastases. The aim was to provide an experimental basis for clinical examination. We randomly assigned male Sprague-Dawley rats to sham and experimental groups. The experimental group constituted a liver cancer model induced by diethylnitrosamine, whereas the sham group was administered with an equivalent volume of normal saline. Gpc3 and Afp mRNA was detected using nested PCR. Analysis was performed to determine statistical significance. Compared with the sham group, the rates of occurrence of Gpc3 and Afp mRNA were significantly higher in the experimental group (P < 0.05). Compared with the total positive ratio of hepatoma cells examined by joint detection, the rates of occurrence of Gpc3 and Afp mRNA increased significantly in the four subgroups of the experimental group (P < 0.05). The use of nested PCR significantly improved sensitivity for the detection of Gpc3 and Afp mRNA in liver cancer micrometastases.
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