康春生, 浦佩玉, 李捷, 于士柱, 王虎, 江荣才, 董伦, 王广秀. 人脑胶质瘤MMP2、MMP9和Ki-67的表达及其相关性的探讨[J]. 中国肿瘤临床, 2004, 31(14): 820-823.
引用本文: 康春生, 浦佩玉, 李捷, 于士柱, 王虎, 江荣才, 董伦, 王广秀. 人脑胶质瘤MMP2、MMP9和Ki-67的表达及其相关性的探讨[J]. 中国肿瘤临床, 2004, 31(14): 820-823.
Kang Chun-sheng, Pu Pei-yu, Li Jie, . The Study on the Expression of MMP2, MMP9 and Ki-67 in Human Gliomas[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2004, 31(14): 820-823.
Citation: Kang Chun-sheng, Pu Pei-yu, Li Jie, . The Study on the Expression of MMP2, MMP9 and Ki-67 in Human Gliomas[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2004, 31(14): 820-823.

人脑胶质瘤MMP2、MMP9和Ki-67的表达及其相关性的探讨

The Study on the Expression of MMP2, MMP9 and Ki-67 in Human Gliomas

  • 摘要: 目的:探讨人脑胶质瘤基质金属蛋白酶MMP2、MMP9和Ki-67的表达及其相关性。方法:应用MMP2、MMP9表达水平代表胶质瘤的侵袭活性,应用Ki-67标记指数代表胶质瘤的增殖活性;用免疫组化方法观察了6例正常脑组织、50例胶质瘤标本和2例恶性胶质瘤体外细胞系的MMP2、MMP9和Ki-67表达,并分析其相关性。结果:在胶质瘤中MMP2、MMP9的阳性表达率和Ki-67LI均随肿瘤恶性程度增加而增加并与胶质瘤分级呈正相关;相关分析发现,MMP2、MMP9和Ki-67LI的表达两两相关。结论:增殖和侵袭在恶性胶质瘤的分子生物学演进过程中相互协同、共同促进肿瘤细胞的恶性进展。

     

    Abstract: Objective : To study the expression of Matrix Metalloproteinase (MMP)2, MMP9 and Ki-67 in human gliomas and the relationship between tumor proliferation and invasion. Methods : Tu-mor invasion was examed as the expression level of (MMP) 2 and MMP9. Proliferative activity of glioma was evaluated by Ki-67 Labling Index (Ki-67 LI) , and Immunohistochemical study was used for Ki-67, MMP2 and MMP9 expression in six normal brain tissue samples, fifty glioma samples and two glioblastoma cell lines. Results : The positive stained-cell rate of MMP2 and MMP9 increased with the degree of malignancy of tumors, and their differences of positive rate and expression level between the low-grade and high-grade tumors were also statistically significant. Ki-67 LI also increased corre-spondingly to the ascending of tumor grade, and the Ki-67 LI in grade III and IV was higher than that in low-grade gliomas. In addition, the expression of MMP2, MMP9 and Ki-67 correlated well with each other by Person correlation analysis. Conclusion : Proliferation and invasion cooperate with each other to promote the development of malignant phenotypes of gliomas.

     

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