Center for Molecular Medicine, University of Connecticut Health Center, 263 Farmington Ave., Farmington, CT 06030-3101, USA.
Biochimie. 2010 Jun;92(6):660-4. doi: 10.1016/j.biochi.2010.02.006. Epub 2010 Feb 13.
Prostaglandin E(2) (PGE(2)) is a bioactive lipid that can elicit a wide range of biological effects associated with inflammation and cancer. The physiological roles of PGE(2) are diverse, mediated in part through activation of key downstream signaling cascades via transmembrane EP receptors located on the cell surface. Elevated levels of COX-2 and concomitant overproduction of PGE(2) are often found in human cancers. These observations have led to the use of non-steroidal anti-inflammatory drugs (NSAIDs) as chemopreventive agents, particularly for colorectal cancer (CRC). Their long-term use, however, may be associated with gastrointestinal toxicity and increased risk of adverse cardiovascular events, prompting the development of other enzymatic targets in this pathway. This review will focus on recent efforts to target the terminal synthase, mPGES-1, for cancer chemoprevention. The role of mPGES-1 in the pathogenesis of various cancers is discussed. In addition, an overview of recent efforts to develop small molecule inhibitors that target the protein with high selectivity is also be reviewed.
前列腺素 E(2)(PGE(2))是一种生物活性脂质,可引起与炎症和癌症相关的广泛的生物学效应。PGE(2) 的生理作用多种多样,部分通过细胞表面的跨膜 EP 受体激活关键下游信号级联来介导。在人类癌症中,通常发现 COX-2 水平升高和 PGE(2)的过度产生。这些观察结果导致了非甾体抗炎药(NSAIDs)作为化学预防剂的使用,特别是用于结直肠癌(CRC)。然而,它们的长期使用可能与胃肠道毒性和不良心血管事件的风险增加有关,促使人们开发该途径中的其他酶靶标。本综述将重点介绍靶向末端合酶 mPGES-1 用于癌症化学预防的最新研究进展。讨论了 mPGES-1 在各种癌症发病机制中的作用。此外,还综述了最近开发针对该蛋白具有高选择性的小分子抑制剂的努力。