肝癌组织膜联蛋白A2异常表达及临床病理特征分析  被引量:2

Abnormal expression of Annexin A2 and its clinicopathologic characteristics in tissues of hepatocellular carcinoma

在线阅读下载全文

作  者:张海健[1] 秦呈林[1] 姚宁华[1] 蔚丹丹[1] 严晓娣[1] 陈洁[1] 姚登福[1] 

机构地区:[1]南通大学附属医院临床医学研究中心,南通226001

出  处:《南通大学学报(医学版)》2012年第2期110-113,F0003,共5页Journal of Nantong University(Medical sciences)

基  金:江苏省高等教育机构优势学科建设(PAPD);南通市社会发展项目(HS2011012)

摘  要:目的:分析肝细胞性肝癌(HCC)组织中膜联蛋白A2(ANXA2)的异常表达及其临床病理学特征。方法:以自身配对法分别收集30例HCC患者经手术切除后的癌灶、癌旁和远癌组织,用免疫组化方法检测组织中ANXA2的表达,分析ANXA2表达的临床病理特征。结果:HCC的癌灶组织中ANXA2定位于细胞的胞膜和胞浆;癌旁组织中ANXA2主要定位于胞浆,而远癌组织中未见ANXA2明显表达。癌灶组织中ANXA2表达强度明显高于癌旁(Z=6.113,P<0.01)和远癌组织(Z=7.328,P<0.01),并且其表达水平与HBV感染和门静脉癌栓有关,而与患者年龄、性别、肿瘤大小、AFP浓度、肿瘤数目和分化程度间差异无统计学意义。结论:HCC组织中ANXA2过表达与HCC的进展有关,是肝癌诊断的有用分子标志物之一。Objective: To investigate the distribution and expression level of Annexin A2(ANXA2) and its clinicopathologic characteristics in tissues of hepatocellular carcinoma(HCC).Methods: HCC,the self-controlled adjacent-,and distant-cancerous tissues were collected from 30 HCC patients.The expression of ANXA2 in these specimens was detected by immunohistochemistry.Results: Positive ANXA2 staining was localized in both cell membrane and cytoplasm in HCC,and only in cytoplasm in their self-controlled adjacent tissue.No positive staining was found in their distant-cancerous tissues.The intensity of ANXA2 expression was significantly higher in HCC tissues more than that in the self-controlled adjacent(Z=6.113,P0.01) or distant-cancerous tissues(Z=7.328,P0.01),correlated with HBV infection and portal vein thrombus,but not with patients'age,sex,tumor size,AFP level,number of tumor,and differentiation degree.Conclusion: Abnormal expression of hepatic ANXA2 was closely associated with the progression of HCC,and its detection could be a useful molecular marker for HCC diagnosis.

关 键 词:肝细胞性肝癌 膜联蛋白A2 免疫组化 临床病理学特征 

分 类 号:R735.7[医药卫生—肿瘤]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象