临床肿瘤学杂志

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肝细胞癌中miR-122的表达及其与血清AFP水平的关系

王跃华1,江 涛1,张 斌1,蔡 凯2,项 方2,贾绍昌2   

  1. 1 210002 南京解放军八一医院全军肿瘤中心肿瘤外科 2 210002 解放军八一医院肿瘤生物治疗中心
  • 收稿日期:2012-05-04 修回日期:2012-06-22 出版日期:2012-08-31 发布日期:2012-08-31
  • 通讯作者: 贾绍昌

Expression of miR-122 in hepatocellular carcinoma and its correlation to serum alpha-fetoprotein

WANG Yue-hua, JIANG Tao,ZHANG Bin,CAI Kai,XIANG Fang,JIA Shao-chang

  

  1. Department of Surgical Oncology, PLA Oncology Center, 81st Hospital of PLA,Nanjing 210002, China
  • Received:2012-05-04 Revised:2012-06-22 Online:2012-08-31 Published:2012-08-31
  • Contact: JIA Shao-chang

摘要:

目的 探讨miR-122在肝细胞癌(肝癌)中的表达水平及其与血清AFP水平的关系。方法 用荧光定量PCR分别检测78例肝癌患者肝癌组织中miR-122的表达水平,电化学发光免疫分析法检测肝癌患者术前血清AFP水平,分析miR-122表达与血清AFP水平的关系。结果78例肝癌患者肿瘤组织miR-122的相对表达量为(23.71±13.33)%,其中高、中分化组织为(26.90±13.64)%,明显高于低分化者的(16.54±9.40)%(P=0.001)。78例肝癌患者血清AFP平均值为(741±382)ng/ml。miR-122表达与性别、年龄、淋巴结转移、肿瘤大小、血管浸润、分期等无关,miR-122在肝癌和癌旁组织中的表达与血清AFP水平呈负相关(r=-0.863,P<0.01)。结论 miR-122表达与血清AFP水平呈负相关,在低分化肝癌中表达更低,提示miR-122是肝癌的一个潜在预后因子。

Abstract:

Objective To investigate the expression of miR-122 in hepatocellular carcinoma(HCC) and its correlation to serum levels of alpha-fetoprotein(AFP). Methods The quantitative reverse transcriptionPCR was used to detect the expression of miR-122 in 78 cases of HCC, and the electrochemical immunoassay was used to detect the levels of AFP in serum before operation. Results In 78 patients of HCC, the expression of miR-122 in tumor tissues was(23.71±13.33)%; the expression in tissues of high and moderate differentiation was(26.90±13.64)%, higher than(16.54±9.40)% in low differentiation tissues(P=0.001). The mean serum AFP level was(741±382) ng/ml in those patients. The expression of miR122 in HCC was negatively correlated with serum AFP level(r=-0.863,P<0.01), but it was not correlated with gender, age, tumor size, lymph node metastasis, vascular invasion and stage. Conclusion miR-122 in HCC is negatively correlated with the serum AFP level, and is expressed lower in low differentiation tissues, which indicates that miR-122 is a potential prognostic factor.

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