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Tyrosinkinasereseptor-ras-ERK-signalveien som terapeutisk mål ved kreft
Engelsk titel: Tyrosine kinase receptor-ras-ERK signal transduction pathway as therapeutic target in cancer Läs online Författare: Leirdal M ; Sioud M Språk: Nor Antal referenser: 31 Dokumenttyp: Översikt UI-nummer: 02021817

Tidskrift

Tidsskrift for Den Norske Laegeforening 2002;122(2)178-82 ISSN 0029-2001 E-ISSN 0807-7096 KIBs bestånd av denna tidskrift Denna tidskrift är expertgranskad (Peer-Reviewed)

Sammanfattning

INTERPRETATION : Inactivation of the receptor tyrosine kinase ras-ERK signalling pathway by small molecular inhibitors has confirmed its involvement in tumour growth. Thus, molecular and/or pharmacological modulation of the components that are critically involved in the constitutive activation of this pathway are expected to improve the treatment of human malignancies. RESULTS : Inhibition of the receptor tyrosine kinase ras-ERK signalling pathway activation by various novel agents (e.g. small molecule tyrosine kinase inhibitors, antibodies, FTase inhibitors, SH2/SH3 directed agents, antisense, ribozymes) impaired tumour growth. Some of the developed agents have been tested in clinical trials; promising results were obtained. MATERIAL AND METHODS : We review the recent progress in establishing novel approaches to interference with the constitutive activation of the receptor tyrosine kinase ras-ERK signalling pathway in cancer. BACKGROUND : Experimental evidence indicates that various intracellular signalling cascades are altered in tumour cells. Among these, the receptor tyrosine kinase ras-ERK signalling pathway was found to be constitutively active in a significant percentage of human tumours; hence, considerable effort has been directed at finding compounds that inhibit its activation.