1.Matrix metalloproteinases in human gliomas: activation of matrix metalloproteinase-2 (MMP-2) may be correlated with membrane-type-1 matrix metalloproteinase (MT1-MMP) expression.
Jin Heang HUR ; Myung Jin PARK ; In Chul PARK ; Dong Hee YI ; Chang Hun RHEE ; Seok Il HONG ; Seung Hoon LEE
Journal of Korean Medical Science 2000;15(3):309-314
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.
Animal
;
Blotting, Northern/methods
;
Brain/pathology
;
Brain Neoplasms/pathology
;
Brain Neoplasms/enzymology*
;
Enzyme Activation
;
Gelatinase A/metabolism
;
Gelatinase A/genetics*
;
Gelatinase B/metabolism
;
Gene Expression Regulation, Enzymologic*
;
Glioma/pathology
;
Glioma/enzymology*
;
Human
;
Metalloendopeptidases/genetics*
;
Papio
;
Tissue Inhibitor-of Metalloproteinase-2/genetics
;
Tissue-Inhibitor of Metalloproteinase-1/genetics
;
Tumor Cells, Cultured
2.Matrix metalloproteinases in human gliomas: activation of matrix metalloproteinase-2 (MMP-2) may be correlated with membrane-type-1 matrix metalloproteinase (MT1-MMP) expression.
Jin Heang HUR ; Myung Jin PARK ; In Chul PARK ; Dong Hee YI ; Chang Hun RHEE ; Seok Il HONG ; Seung Hoon LEE
Journal of Korean Medical Science 2000;15(3):309-314
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.
Animal
;
Blotting, Northern/methods
;
Brain/pathology
;
Brain Neoplasms/pathology
;
Brain Neoplasms/enzymology*
;
Enzyme Activation
;
Gelatinase A/metabolism
;
Gelatinase A/genetics*
;
Gelatinase B/metabolism
;
Gene Expression Regulation, Enzymologic*
;
Glioma/pathology
;
Glioma/enzymology*
;
Human
;
Metalloendopeptidases/genetics*
;
Papio
;
Tissue Inhibitor-of Metalloproteinase-2/genetics
;
Tissue-Inhibitor of Metalloproteinase-1/genetics
;
Tumor Cells, Cultured