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[Kinase inhibitors for the therapy of malignant melanoma].
- Source :
-
Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG [J Dtsch Dermatol Ges] 2005 Oct; Vol. 3 (10), pp. 762-7. - Publication Year :
- 2005
-
Abstract
- Recent results from basic and translational research on the causes and mechanisms of melanoma genesis and progression will impact on future therapeutic approaches. The increasing understanding of the molecular pathology of malignant disease and the detailed analysis of the signal transduction pathways involved allows specific intervention with these oncogenic events. These interventions address the molecules associated with or responsible for the malignant transformation and have therefore been termed "targeted therapy". The present review focuses on the therapeutic options involving modulation of the Ras/MAPK- and PI3K/AKT-signal transduction pathways.
- Subjects :
- Animals
Apoptosis drug effects
Apoptosis genetics
Cell Survival drug effects
Cell Survival genetics
Cell Transformation, Neoplastic drug effects
Cell Transformation, Neoplastic genetics
Genes, ras drug effects
Genes, ras genetics
Humans
Melanoma genetics
Mitogen-Activated Protein Kinase Kinases antagonists & inhibitors
Mitogen-Activated Protein Kinase Kinases genetics
Oncogene Protein v-akt antagonists & inhibitors
Oncogene Protein v-akt genetics
Phosphatidylinositol 3-Kinases genetics
Phosphoinositide-3 Kinase Inhibitors
Protein Biosynthesis drug effects
Protein Biosynthesis genetics
Skin Neoplasms genetics
Antineoplastic Agents therapeutic use
Melanoma drug therapy
Phosphotransferases antagonists & inhibitors
Skin Neoplasms drug therapy
Subjects
Details
- Language :
- German
- ISSN :
- 1610-0379
- Volume :
- 3
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
- Publication Type :
- Academic Journal
- Accession number :
- 16194153
- Full Text :
- https://doi.org/10.1111/j.1610-0387.2005.05016.x