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Stimulatory versus suppressive effects of GM-CSF on tumor progression in multiple cancer types
Experimental & Molecular Medicine ; : e242-2016.
Article Dans Anglais | WPRIM | ID: wpr-167180
ABSTRACT
Granulocyte-macrophage colony-stimulating factor (GM-CSF, also called CSF-2) is best known for its critical role in immune modulation and hematopoiesis. A large body of experimental evidence indicates that GM-CSF, which is frequently upregulated in multiple types of human cancers, effectively marks cancer cells with a ‘danger flag' for the immune system. In this context, most studies have focused on its function as an immunomodulator, namely its ability to stimulate dendritic cell (DC) maturation and monocyte/macrophage activity. However, recent studies have suggested that GM-CSF also promotes immune-independent tumor progression by supporting tumor microenvironments and stimulating tumor growth and metastasis. Although some studies have suggested that GM-CSF has inhibitory effects on tumor growth and metastasis, an even greater number of studies show that GM-CSF exerts stimulatory effects on tumor progression. In this review, we summarize a number of findings to provide the currently available information regarding the anticancer immune response of GM-CSG. We then discuss the potential roles of GM-CSF in the progression of multiple types of cancer to provide insights into some of the complexities of its clinical applications.
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Cellules dendritiques / Facteur de stimulation des colonies de granulocytes et de macrophages / Microenvironnement tumoral / Hématopoïèse / Système immunitaire / Métastase tumorale Limites du sujet: Humains langue: Anglais Texte intégral: Experimental & Molecular Medicine Année: 2016 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Cellules dendritiques / Facteur de stimulation des colonies de granulocytes et de macrophages / Microenvironnement tumoral / Hématopoïèse / Système immunitaire / Métastase tumorale Limites du sujet: Humains langue: Anglais Texte intégral: Experimental & Molecular Medicine Année: 2016 Type: Article