Dissection of signaling in inflammation: three novel inflammatory regulators.

Cold Spring Harb Symp Quant Biol

The Campbell Family Institute for Breast Cancer Research and Ontario Cancer Institute, University Health Network, Toronto, Ontario M5G 2C1, Canada

Published: March 2015

AI Article Synopsis

  • Uncontrolled inflammation plays a key role in autoimmune diseases and might contribute to cancer development.
  • Identifying molecules that can regulate inflammation is essential for creating new treatment options for these conditions.
  • This review focuses on three important molecules—MALT1, Ariadne-2, and acetylcholine—and their roles in controlling inflammation and activating related signaling pathways.

Article Abstract

Uncontrolled inflammation is a feature of autoimmune diseases and autoinflammatory syndromes and may promote tumorigenesis. Thus, identifying molecules that regulate the signaling pathways triggering, mediating, and suppressing inflammation could be helpful in developing new therapeutic approaches for these debilitating diseases. In this review, we present new information on three molecules with important roles in controlling inflammation: MALT1, Ariadne-2, and acetylcholine. We summarize our current state of knowledge of how these molecules function, and how they are involved in pathways of NF-κB activation or vagal nerve stimulation associated with inflammation.

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Source
http://dx.doi.org/10.1101/sqb.2013.78.020107DOI Listing

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