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Antisense Deoxyoligonucleotides Inhibit Activities of Matrix Metalloproteinase-2 in Human Fibrosarcoma HT1080 Cells / Journal of the Korean Cancer Association, 대한암학회지
Cancer Research and Treatment ; : 444-449, 2002.
Article Dans Anglais | WPRIM | ID: wpr-27225
ABSTRACT

PURPOSE:

MMP-2, 72 kDa-type IV collagenase, plays a major role in the migration and growth of tumor cells, a process that requires the disintegration of basement membrane. Activation of MMP-2 is correlated with the invasiveness of various tumors. The aim of this study was to determine the sequence-specific phosphorothioated oligodeoxynucleotides (ODNs) inhibiting the translation of MMP-2 mRNA and the subsequent invasiveness of tumor cells. MATERIALS AND

METHODS:

Eight types of antisense ODNs were designed and each (8micro gram/ml) were transfected into HT1080 cells. The effects of these antisense ODNs on MMP expression were examined by gelatin zymography, Western blot, Northern blot and matrigel assay.

RESULTS:

Antisense-5 (+904~923), antisense-6 (+1274~+1293) and antisense-7 (+1646~+1665) reduced the MMP-2 activity of the culture supernatant in HT1080 fibrosarcoma cells. Treatment with antisense-6 showed inhibition of MMP-2 mRNA and protein, and in vitro invasion in a dose-dependent manner.

CONCLUSION:

Antisense-6 might be one of the therapeutic candidates for tumor invasion and metastasis.
Sujets)

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Oligodésoxyribonucléotides / Membrane basale / ARN messager / Technique de Western / Technique de Northern / Collagenases / Matrix metalloproteinase 2 / Fibrosarcome / Gélatine / Métastase tumorale Limites du sujet: Humains langue: Anglais Texte intégral: Cancer Research and Treatment Année: 2002 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Oligodésoxyribonucléotides / Membrane basale / ARN messager / Technique de Western / Technique de Northern / Collagenases / Matrix metalloproteinase 2 / Fibrosarcome / Gélatine / Métastase tumorale Limites du sujet: Humains langue: Anglais Texte intégral: Cancer Research and Treatment Année: 2002 Type: Article