Laboratoire de Biologie Moléculaire et Cellulaire de Cancer, Hôpital Kirchberg, 9, rue Edward Steichen, L 2540 Luxembourg, Luxembourg.
Curr Top Med Chem. 2012;12(13):1392-407. doi: 10.2174/156802612801784416.
TNF-α was discovered more then 20 years ago as a cytokine implicated in a wide range of cell signaling pathways, many of which are known to lead to the activation of genes involved in inflammation and carcinogenesis. TNF-α is involved in the pathogenesis of many diseases, including Crohn's disease, diabetes, septic shock, tumorigenesis, rheumatoid arthritis, psoriatic arthritis and inflammatory bowel disease. Multidisciplinary research endeavoring to understand the biomolecular and biomedicinal properties of TNF-α has never faded away, and the search for natural products able to inhibit TNF-α remains, to date, a hot topic of investigation. Over the last 10 years, many TNF-α-inhibiting natural compounds have been discovered, and their anti-TNF-α activities have been described. The present review describes the major cell signaling pathways activated by TNF-α and discusses the chemical and biological properties of TNF-α-inhibiting natural products, focusing on compounds that are able to inhibit TNF-α-related signal transduction pathways or TNF-α gene expression.
TNF-α 是 20 多年前发现的一种细胞因子,涉及多种细胞信号通路,其中许多通路已知可导致参与炎症和肿瘤发生的基因激活。TNF-α 参与许多疾病的发病机制,包括克罗恩病、糖尿病、感染性休克、肿瘤发生、类风湿关节炎、银屑病关节炎和炎症性肠病。旨在了解 TNF-α 的生物分子和生物医学特性的多学科研究从未停止过,迄今为止,寻找能够抑制 TNF-α 的天然产物仍然是一个热门研究课题。在过去的 10 年中,已经发现了许多抑制 TNF-α 的天然化合物,并描述了它们的抗 TNF-α 活性。本综述描述了 TNF-α 激活的主要细胞信号通路,并讨论了抑制 TNF-α 的天然产物的化学和生物学特性,重点介绍了能够抑制 TNF-α 相关信号转导通路或 TNF-α 基因表达的化合物。