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缝隙连接蛋白43和胰岛素样生长因子Ⅰ与脑胶质瘤恶性程度的相关性研究
引用本文:万跃明,袁俊峰,石浩,樊启涛,袁先厚,江普查,文志华. 缝隙连接蛋白43和胰岛素样生长因子Ⅰ与脑胶质瘤恶性程度的相关性研究[J]. 中国临床神经外科杂志, 2007, 12(1): 22-24
作者姓名:万跃明  袁俊峰  石浩  樊启涛  袁先厚  江普查  文志华
作者单位:1. 湖北省武警医院神经外科,湖北武汉,430061
2. 武汉大学中南医院神经外科,湖北武汉,430071
摘    要:目的 探讨缝隙连接蛋白43(cx43)、胰岛素样生长因子Ⅰ(IGF-Ⅰ)和细胞核相关抗原Ki-67在人脑胶质瘤中的表达及相关性。方法 采用免疫组织化学SP法检测45例胶质瘤组织和10例正常脑组织中Cx43、IGF-Ⅰ、Ki-67的表达。结果 Cx43在Ⅰ-Ⅱ级脑胶质瘤中阳性表达率为87.5%,Ⅲ-Ⅳ级中的阳性表达率为42.9%,两者间的差异有显著性(P〈0.01),且随Ki-67表达升高而降低(r=-0.893,P〈0.01);IGFⅠ在Ⅰ-Ⅱ级脑胶质瘤中的表达(阳性率58.3%)与在Ⅲ-Ⅳ级(阳性率85.7%)中的表达差异有显著性(P〈0.05),且与Cx43的表达呈明显负相关(r=-0.688,P〈0.01)。结论 Cx43表达水平的下调或缺失不是胶质瘤发生的始动因素,可能是胶质瘤恶性演进过程中的一个重要分子事件,促使肿瘤细胞恶性增殖程度增加。

关 键 词:胶质瘤  CX43蛋白  IGF-Ⅰ  免疫组织化学
文章编号:23660325
修稿时间:2006-05-30

Relationship of Cx43 and IGF-Ⅰ with Malignancy Degree of Human Glioma
WAN Yue-ming, YUAN Jun-feng, SHI Hao,et al.. Relationship of Cx43 and IGF-Ⅰ with Malignancy Degree of Human Glioma[J]. Chinese Journal of Clinical Neurosurgery, 2007, 12(1): 22-24
Authors:WAN Yue-ming   YUAN Jun-feng   SHI Hao  et al.
Affiliation:Department of Neurosurgery, Hospital of Hubei Province Armed Police Corps, Wuhan Hubei 430061, China
Abstract:Objective To explore connexin 43(Cx43) gene, insulin-like growth fator-Ⅰ (IGF-Ⅰ ) and Ki-67 expressions in human glioma and the relationship among them. Methods Expressions of Cx43, IGF-Ⅰ and Ki-67 were determined by immunohistochemistry staining in 45 cases of gliomas and 10 cases of normal brain tissues. Results The positive rate of Cx43 expression was 87.5% (21124) in th..e low grade (WHO grade Ⅰ -Ⅱ ) gliomas, and 42.9%(9121) in the high grade (WHO grade Ⅲ-Ⅳ) gliomas. There was significant difference in the positive rate of Cx43 expression between the low and high grades gliomas (P〈0.01).In the gliomas the expression of Cx43 was negatively related with Ki-67 expression (r=-0.893, P〈0.01). The positive rate of IGF-Ⅰ expression in the low grade gliomas (58.3%, 14124) was significantly lower (P〈0.05) than that in the high grade gliomas (85.7%, 18/21). In the gliomas the IGF-Ⅰ expression was negative related with Cx43 expression (r=-0.688, P〈0.01). Conclusion The deficiency or down regulation of Cx43 expression is not a factor producing gliomas occurrence,but maybe it promotes proliferation and development of the glioma cells.
Keywords:Glioma  Cx43 protein  IGF- Ⅰ  Immunohistochemistry
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