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Signal transduction targets in Kaposi's sarcoma

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CURRENT OPINION IN ONCOLOGY
卷 18, 期 5, 页码 456-462

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/01.cco.0000239884.05914.13

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angiogenesis; Kaposi's sarcoma; therapy; tyrosine kinase inhibitor

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Purpose of review AIDS-related Kaposi's sarcoma results from co-infection with HIV and Kaposi's sarcoma herpesvirus/human herpesvirus-8, which leads: to the development of an angiogenic-inflammatory state that is critical in the pathogenesis of the condition: Recent discoveries regarding Kaposi's sarcoma herpesvirus/human herpesvirus-8 infection and its activation of signal transduction have led to a greater understanding into Kaposi's sarcoma pathogenesis and have identified potential targets for therapy. Recent findings Kaposi's sarcoma is driven by Kaposi's sarcoma herpesvirus/human herpesvirus-8-specific pathways, which include viral G protein-coupled receptor, viral IL-6, and viral chemokine homologues: In addition; cellular growth/angiogenic pathways such as vascular, endothelial growth factor, insulin growth factor; platelet-derived growth factor, angiopoietin and matrix metalloproteinases are 'pirated' by Kaposi's sarcoma herpesvirus/human herpesvirus-8. Recent findings show Kaposi's sarcoma herpesvirus/human herpesvirus-8 specific signaling pathways and pirated pathways to be important therapeutic targets. Summary, Numerous advances have been made recently that expand the understanding of Kaposi's sarcoma pathogenesis. These findings and recent clinical trials of targeted therapy for treatment are a prelude to a shift in the paradigm of how AIDS-related Kaposi's sarcoma is managed.

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