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MMP-2/TIMP-2在妊娠滋养细胞疾病组织中的表达及意义
引用本文:丁峰,张秋实,邢福祺. MMP-2/TIMP-2在妊娠滋养细胞疾病组织中的表达及意义[J]. 南方医科大学学报, 2007, 27(2): 150-152
作者姓名:丁峰  张秋实  邢福祺
作者单位:1. 山东济南市解放军456医院妇产科,250031
2. 中山大学博士后流动站,广东,广州,510120
3. 南方医科大学南方医院妇产科,广东,广州,510515
基金项目:国家重点基础研究发展计划(973计划)
摘    要:目的 探讨金属基质蛋白酶-明胶酶A(MMP-2)及其抑制剂(TIMP-2)在妊娠滋养细胞疾病发生、发展及预后中的作用.方法 采用原位杂交、免疫组化法分别从mRNA、蛋白质水平检测MMP-2/TIMP-2在正常早孕绒毛及妊娠滋养细胞疾病中的表达.结果 未恶性转化葡萄胎MMP-2低表达,TIMP-2高表达,恶性转化葡萄胎、侵蚀性葡萄胎、绒癌中MMP-2表达逐渐增强,TIMP-2表达相反.妊娠滋养细胞肿瘤组与正常绒毛、葡萄胎组相比,MMP-2、TIMP-2的表达均有显著性差异(P<0.01,P<0.001).结论 金属基质蛋白酶的激活与抑制比例失衡在妊娠滋养细胞疾病发展、浸润和转移中起重要作用.

关 键 词:妊娠滋养细胞疾病  金属基质蛋白酶-明胶酶A  金属基质蛋白酶抑制剂2
文章编号:1673-4254(2007)02-0150-03
收稿时间:2006-02-11
修稿时间:2006-02-11

MMP-2/TIMP-2 expression in the trophoblasts of patients with gestational trophoblastic disease
DING Feng,ZHANG Qiu-shi,XING Fu-qi. MMP-2/TIMP-2 expression in the trophoblasts of patients with gestational trophoblastic disease[J]. Journal of Southern Medical University, 2007, 27(2): 150-152
Authors:DING Feng  ZHANG Qiu-shi  XING Fu-qi
Affiliation:Postdocboral Station, Sun Yet-sen University, Guangzhou 510120, China. dfsyw@sina.com
Abstract:Objectative To explore the role of matrix metalloproteinase-2 (MMP-2) and tissue inhibitor of MMP-2 (TIMP-2) in the pathogenesis, development and prognosis of gestational trophoblastic disease (GTD). Methods In situ hybridization and immunohistochemistry were utilized for MMP-2/TIMP-2 mRNA and protein detection in normal chorion of women with early gestation, hydatidiform mole, invasive mole, or choricarcinoma. Results The results revealed that specific staining for mRNA and protein of MMP-2 and the expression of TIMP-2 was reduced in normal chorion of early gestation. In GTD ranging from hydatidiform mole, invasive mole to choricarcinoma, MMP-2 expression tended to increase while TIMP-2 expression underwent an invert change. The positivity rate of MMP-2 and TIMP-2 in gestational trophoblastic tumor group was higher than that of the normal chorion of early gestation group and hydatiform mole group (P<0.05 and P<0.001, respectively). Conclusion A disrupted balance between the activation and inhibition of MMP-2 plays a critical role in the pathogenesis, progression and metastasis of GTD.
Keywords:gestational trophoblastic disease   matrix metalloproteinase-2   tissue inhibitor, matrix metalloproteinase-2
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