Signal Transduction Pathways and Transcription Factors as Therapeutic Targets in Inflammatory Disease: Towards Innovative Antirheumatic Therapy

信号转导 PI3K/AKT/mTOR通路 炎症 转录因子 蛋白激酶B MAPK/ERK通路 细胞生物学 激酶 癌症研究 免疫学 医学 生物 生物化学 基因
作者
Sander W. Tas,Phj Remans,Kris A. Reedquist,Paul P. Tak
出处
期刊:Current Pharmaceutical Design [Bentham Science Publishers]
卷期号:11 (5): 581-611 被引量:78
标识
DOI:10.2174/1381612053381918
摘要

Many chronic inflammatory diseases are associated with deregulated intracellular signal transduction pathways. Resultant pathogenic interactions between immune and stromal cells lead to changes in cell activation, proliferation, migratory capacity, and cell survival that all contribute to inflammation. Increasing efforts are now being made in the design of novel therapeutic compounds to interfere with signaling pathways in inflammatory diseases like rheumatoid arthritis (RA). In this review we will outline the major signal transduction pathways involved in the pathogenesis of RA. We will assess advances in targeting a number of key intracellular pathways, including nuclear factor-κB (NF-κB), mitogen-associated protein kinases (MAPKs), phosphoinositide 3-kinase (PI3K) / Akt, signal transducers and activators of transcription (STATs), and reactive oxygen species (ROS) production. Finally, we will discuss recently identified lead molecules and the progress of selected compounds towards becoming new drugs for the treatment of inflammatory diseases. Keywords: inflammatory disease, rheumatoid arthritis, signal transduction, nuclear factor, mitogen-activated protein kinase, reactive oxygen species, novel therapies

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