人脑胶质瘤白介素13受体基因表达与肿瘤增殖活性的关系研究  被引量:3

Expression of interleukin-13 receptor and its relationship to proliferation activity of human gliomas

在线阅读下载全文

作  者:夏之柏[1] 吴新建[1] 齐铁伟[1] 王海军[1] 黄正松[1] 

机构地区:[1]中山大学附属第一医院神经外科,广州510080

出  处:《中华显微外科杂志》2006年第6期438-441,共4页Chinese Journal of Microsurgery

基  金:教育部博士点专项基金(099004);第三十一期中国博士后基金

摘  要:目的探讨人脑胶质瘤白介素13受体(IL-13R)基因表达与肿瘤增殖活性的关系。方法对6例正常脑组织,50例人脑胶质瘤和2个脑瘤体外细胞系采用RT-PCR法和免疫组织化学法检测IL-13R。结果人脑胶质瘤组织IL-13RαmRNA总阳性表达率70%,正常脑组织中仅1例有极弱的表达;2例恶性胶质瘤体外细胞系均高表达。IL-13RαmRNA表达率和表达丰度与胶质瘤分级(前者rs=0.87,P<0.01;后者rs=0.69,P<0.01)、肿瘤增殖活性Ki-67LI(r=0.64,P<0.01)呈正相关,即胶质瘤恶性程度越高,IL-13RαmRNA表达率和表达水平越高。结论IL-13Rα基因在人脑胶质瘤中表达上升,与肿瘤的分级和肿瘤增殖活性呈正相关,可作为预测某些肿瘤治疗效果及监测复发的指标之一。Objective To explore the gene expression of interleukin-13 receptor (IL-13R) α2 and its relationship to proliferation activity of human gliomas. Methods The gene expression of IL-13Rαin 50 human gliomas, 2 malignant human glioma cell lines and 6 normal brain tissues were studied by RT-PCR. Ki-67 labeling index ( Ki267 LI) of all sample were detecteded by immunohistochemical staining. Results Only one normal brain tissues expressed very low IL-13R α2 mRNA, whereas 35(70% ) of 50 human brain tumors expressed IL-13R α2 mRNA. The positive rate and expression level of IL-13R α2 mRNA were increased with the ascending of WHO tumor grade. (former: rs =0. 87; letter: rs =0. 69,P 〈0. 01 ). The difference of positive rate and expression level of IL-13R 2α mRNA between the low grade and high grade tumors was statistically significant, the proliferation activity of gliomas evaluated by Ki-67LI (Ki-67 Labeling Index, Ki-67LI) was positively correlated with IL-13R α2 gene expression and the tumor grade. Conclusion In human cerebral gliomas, IL-13R α2 genes may play an role in the malignant progression. The expression level of malignancy in molecular level and selecting the target of gene therapy.

关 键 词:胶质瘤 白介素13受体 基因表达 

分 类 号:R739.4[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