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Expression of Cell Surface Receptors on Human Glioblastoma Xenograft Model in NOD/SCID Mouse / Journal of the Korean Cancer Association, 대한암학회지
Cancer Research and Treatment ; : 52-57, 2002.
Article Dans Coréen | WPRIM | ID: wpr-203236
ABSTRACT

PURPOSE:

To obtain basic data for development of a glioblastoma-specific immunotoxin, the expression of variable cell surface receptors on a human glioblastoma xenograft model was evaluated, using NOD/SCID mice. MATERIALS AND

METHODS:

We developed a xenograft model in NOD/SCID mice implanted with a human glioblastoma cell line (U-87MG). Immunohistochemical studies were performed on implanted tumor nodules (n=8) using antibodies against CD71, EGFR, IGF-IRalpha, CXCR4 and IL-4Ralpha.

RESULTS:

Expression of IL-4Ralpha, in implanted tumornodules, was the highest of the cell surface receptors evaluated in this study. However, the endothelial cells in, and around, the tumor nodules also revealed immunopositivity against IL-4Ralpha. The immunoreactivity of IL-4Ralpha, and other surface receptors such as CD71, IGF-IRalpha and EGFR, was prominent in tumor nodules associated with tumor necrosis.

CONCLUSION:

IL-4Ralpha would be a possible target for the development of glioblastoma-specific immunotoxin, although there are limitations due to its endothelial expression.
Sujets)

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Lignée cellulaire / Immunotoxines / Souris SCID / Glioblastome / Récepteurs de surface cellulaire / Cellules endothéliales / Hétérogreffes / Anticorps / Nécrose Limites du sujet: Animaux / Humains langue: Coréen Texte intégral: Cancer Research and Treatment Année: 2002 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Lignée cellulaire / Immunotoxines / Souris SCID / Glioblastome / Récepteurs de surface cellulaire / Cellules endothéliales / Hétérogreffes / Anticorps / Nécrose Limites du sujet: Animaux / Humains langue: Coréen Texte intégral: Cancer Research and Treatment Année: 2002 Type: Article