欢迎访问《标记免疫分析与临床》官方网站!
临床研究

AEG-1、β-catenin和C-myc在原发性肝细胞癌中的临床特性与分析

展开
  • 贵阳医学院 临床医学院 感染科,贵州 贵阳 550001

收稿日期: 2015-05-15

  修回日期: 2015-06-05

  网络出版日期: 2015-09-16

Clinical Feature Analysis of AEG-1, β-catenin and C-myc Expression in Primary Hepatocellular Carcinoma

Expand
  • Infectious Disease Department, Clinical Medical Institute, Guiyang Medical College, Guiyang 550001, China

Received date: 2015-05-15

  Revised date: 2015-06-05

  Online published: 2015-09-16

摘要

摘要:目的  了解AEG-1、β-catenin和C-myc在原发性肝细胞癌中的临床特性并进行分析。方法  以40例原发性肝癌患者术后肝癌组织作为研究对象;采集肝癌患者的临床及病理学特征,采用免疫组织化学染色及Western Blot方法测定肝癌组织中的AEG-1、β-catenin及C-myc蛋白细胞表达水平及表达载量,分析其表达情况与患者临床及病理特征的关联性。 结果  AEG-1在肝癌组织的高表达率为72.5%,以AOD值记分为0.80±0.07,Western Blot测出相对表达量为1.56±0.12;β-catenin蛋白在肝癌组织中高表达率为75.0%,以AOD值记为0.75±0.06,Western Blot测出相对表达量为1.23±0.11;C-myc的高表达率为62.5%,以AOD值记为0.69±0.06、Western Blot测出相对表达量为1.15±0.09。AEG-1、β-catenin和C-myc蛋白在肝癌组织中的表达与肿瘤TNM分期和肝癌组织病理分化程度有关(P<0.05),差异有统计学意义;与患者的性别、年龄、肿瘤大小、HBsAg、术前AFP浓度均无明显相关(P>0.05),差异无统计学意义。结论  AEG-1、β-catenin和C-myc有望成为评价原发性肝癌恶性程度的指导性指标,进而可以用于评估病程进展及预后; AEG-1、β-catenin和C-myc蛋白在原发性肝癌起病过程中的作用途径独立于AFP系统,为进一步研究原发性肝癌的发病机制提供了新的思路。

关键词: 肝癌; AEG-1; β -catenin; C-myc

本文引用格式

程云娟,罗新华,程明亮 . AEG-1、β-catenin和C-myc在原发性肝细胞癌中的临床特性与分析[J]. 标记免疫分析与临床, 2015 , 22(7) : 633 . DOI: 10.11748/bjmy.issn.1006-1703.2015.07.013

Abstract

Abstract: Objective To investigate the expression level of AEG-1, β-catenin and C-myc in primary hepatocellular carcinoma. Methods 40 cases of primary hepatocellular carcinoma tissue were used as study samples. The clinical and pathological features of liver cancer patients were recorded. The expression level of AEG-1, β-catenin and C-myc were determined by using immunohistochemistry and Western Blot method. Results The expression rate of AEG-1, β-catenin protein and C-myc in primary hepatocellular carcinoma tissues were 72.5%, 75.0% and 62.5%; the AOD value score were 0.80 ± 0.07, 0.75 ± 0.06 and 0.69 ± 0.06; and the relative expression level was 1.56 ± 0.12, 1.23 ± 0.11 and 1.15 ± 0.09, respectively. The expression level of three protein were correlated with pathologic stage differentiation and TNM stage (P <0.05). There was no significant correlation with patient's gender, age, tumor size, HBsAg, and preoperative AFP concentration (P> 0.05). Conclusion AEG-1, β-catenin and C-myc might become guidance indexes for malignant hepatocellular carcinoma evaluation, and can be used to assess disease progression and prognosis. The role of AEG-1, β-catenin and C-myc protein in the original recurrent hepatocellular carcinoma onset process pathway may be independent from AFP system.
Options
文章导航

/