Abstract
Diterpene derivatives of the natural product acanthoic acid have potent anti-inflammatory effects in vivo. In this issue of Chemistry & Biolgy, Través and colleagues report that the primary molecular mechanism of action of diterpenes structurally related to acanthoic acid is the direct activation of PI3-kinase signaling in macrophages, which in turn inhibits NF-κB activation and suppresses proinflammatory gene expression.
Copyright © 2014 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, N.I.H., Extramural
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Comment
MeSH terms
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Animals
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Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
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Class Ia Phosphatidylinositol 3-Kinase / chemistry*
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Class Ia Phosphatidylinositol 3-Kinase / metabolism*
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Diterpenes / pharmacology*
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NF-kappa B / antagonists & inhibitors*
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Protein Subunits / metabolism*
Substances
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Anti-Inflammatory Agents, Non-Steroidal
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Diterpenes
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NF-kappa B
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Protein Subunits
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acanthoic acid
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Class Ia Phosphatidylinositol 3-Kinase