首页> 外文OA文献 >Matrix metalloproteinases in human gliomas: activation of matrix metalloproteinase-2 (MMP-2) may be correlated with membrane-type-1 matrix metalloproteinase (MT1-MMP) expression.
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Matrix metalloproteinases in human gliomas: activation of matrix metalloproteinase-2 (MMP-2) may be correlated with membrane-type-1 matrix metalloproteinase (MT1-MMP) expression.

机译:人脑胶质瘤中的基质金属蛋白酶:基质金属蛋白酶2(MMP-2)的激活可能与膜1型基质金属蛋白酶(MT1-MMP)的表达有关。

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摘要

To evaluate possible roles of matrix metalloproteinase (MMP)-1, -2, tissue inhibitor of metalloproteinase (TIMP)-1, -2 and membrane-type-1 matrix metalloproteinase (MT1-MMP) in invasion of human gliomas, expressions of these proteins were investigated in ten cases of human glioma and two meningioma tissues and eight human glioma cell lines. In gelatin zymography, MMP-2 activities of glioblastomas were higher than astrocytomas. The activated form of MMP-2 was seen in five of six cases of glioblastomas, but not in astrocytomas. MMP-9 activity was detected in all cases of malignant astrocytomas but the reactivity of MMP-9 was weaker than that of MMP-2. MT1-MMP mRNA expression in glioblastomas was higher than that in astrocytomas. Five cases of glioblastomas with activated form of MMP-2 had MT1-MMP expressions. In vitro, human glioma cell lines with high expression of MT1-MMP also showed high MMP-2 activity. TIMP-1 transcripts were constitutively present in almost all glioma tissues and cell lines, whereas TIMP-2 mRNA were weak especially in malignant gliomas. Imbalance of TIMP-2/MMP-2 was observed using immunoprecipitation analysis in a glioma cell line. High expression of MMP-2 and MT1-MMP is possibly involved in invasiveness of malignant glioma.
机译:为了评估基质金属蛋白酶(MMP)-1,-2,金属蛋白酶组织抑制剂(TIMP)-1,-2和膜1型基质金属蛋白酶(MT1-MMP)在人类胶质瘤侵袭中的可能作用,其表达在十例人类神经胶质瘤,两个脑膜瘤组织和八种人类神经胶质瘤细胞系中研究了蛋白质。在明胶酶谱中,胶质母细胞瘤的MMP-2活性高于星形细胞瘤。在6例胶质母细胞瘤病例中,有5例发现了MMP-2的活化形式,但星形细胞瘤中没有。在所有恶性星形细胞瘤病例中均检测到MMP-9活性,但MMP-9的反应性较MMP-2弱。胶质母细胞瘤中MT1-MMP mRNA的表达高于星形细胞瘤。五例激活形式的MMP-2的胶质母细胞瘤患者具有MT1-MMP表达。在体外,高表达MT1-MMP的人神经胶质瘤细胞系也显示出高MMP-2活性。在几乎所有神经胶质瘤组织和细胞系中组成性存在TIMP-1转录本,而TIMP-2 mRNA弱,尤其是在恶性神经胶质瘤中。使用脑胶质瘤细胞系中的免疫沉淀分析观察到TIMP-2 / MMP-2失衡。 MMP-2和MT1-MMP的高表达可能与恶性神经胶质瘤的浸润有关。

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