• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
mPGES-1 as a target for cancer suppression: A comprehensive invited review "Phospholipase A2 and lipid mediators".mPGES-1 作为癌症抑制的靶点:全面邀请评论“磷脂酶 A2 和脂质介质”。
Biochimie. 2010 Jun;92(6):660-4. doi: 10.1016/j.biochi.2010.02.006. Epub 2010 Feb 13.
2
Inhibitors of the microsomal prostaglandin E(2) synthase-1 as alternative to non steroidal anti-inflammatory drugs (NSAIDs)--a critical review.作为非甾体抗炎药(NSAIDs)的替代物,微粒体前列腺素 E(2)合酶-1 抑制剂——批判性评价。
Curr Med Chem. 2009;16(32):4274-96. doi: 10.2174/092986709789578178.
3
Membrane prostaglandin E synthase-1: a novel therapeutic target.膜前列腺素E合酶-1:一种新型治疗靶点。
Pharmacol Rev. 2007 Sep;59(3):207-24. doi: 10.1124/pr.59.3.1.
4
Characterization of microsomal prostaglandin E synthase 1 inhibitors.微粒体前列腺素 E 合酶 1 抑制剂的特性。
Basic Clin Pharmacol Toxicol. 2014 Jan;114(1):64-9. doi: 10.1111/bcpt.12162. Epub 2013 Nov 11.
5
Microsomal prostaglandin E synthase-1 and 5-lipoxygenase: potential drug targets in cancer.微粒体前列腺素 E 合酶-1 和 5-脂氧合酶:癌症的潜在药物靶点。
J Intern Med. 2010 Jul;268(1):5-14. doi: 10.1111/j.1365-2796.2010.02246.x. Epub 2010 Apr 28.
6
Genetic deletion of mPGES-1 suppresses intestinal tumorigenesis.mPGES-1基因缺失可抑制肠道肿瘤发生。
Cancer Res. 2008 May 1;68(9):3251-9. doi: 10.1158/0008-5472.CAN-07-6100.
7
MF63 [2-(6-chloro-1H-phenanthro[9,10-d]imidazol-2-yl)-isophthalonitrile], a selective microsomal prostaglandin E synthase-1 inhibitor, relieves pyresis and pain in preclinical models of inflammation.MF63 [2-(6-氯-1H-菲并[9,10-d]咪唑-2-基)-间苯二甲腈],一种选择性微粒体前列腺素E合酶-1抑制剂,可缓解炎症临床前模型中的发热和疼痛。
J Pharmacol Exp Ther. 2008 Sep;326(3):754-63. doi: 10.1124/jpet.108.138776. Epub 2008 Jun 4.
8
Prostaglandin E synthase, a terminal enzyme for prostaglandin E2 biosynthesis.前列腺素E合酶,一种前列腺素E2生物合成的末端酶。
J Biochem Mol Biol. 2005 Nov 30;38(6):633-8. doi: 10.5483/bmbrep.2005.38.6.633.
9
Identification and development of mPGES-1 inhibitors: where we are at?mPGES-1 抑制剂的鉴定和开发:我们现在处于什么阶段?
Future Med Chem. 2011 Nov;3(15):1909-34. doi: 10.4155/fmc.11.136.
10
Selective inducible microsomal prostaglandin E(2) synthase-1 (mPGES-1) inhibitors derived from an oxicam template.从昔布类模板衍生的选择性诱导性微粒体前列腺素 E2 合酶-1(mPGES-1)抑制剂。
Bioorg Med Chem Lett. 2010 Mar 1;20(5):1604-9. doi: 10.1016/j.bmcl.2010.01.060. Epub 2010 Jan 25.

引用本文的文献

1
Design, synthesis and characterization of lead compounds as anti-inflammatory drugs targeting mPGES-1 via enzymelink screening.通过酶联筛选设计、合成并鉴定靶向 mPGES-1 的先导化合物作为抗炎药物。
Future Med Chem. 2023 May;15(9):757-767. doi: 10.4155/fmc-2023-0039. Epub 2023 May 30.
2
Novel 1,2,4-triazoles derived from Ibuprofen: synthesis and in vitro evaluation of their mPGES-1 inhibitory and antiproliferative activity.新型 1,2,4-三唑类衍生物来源于布洛芬:合成及其对 mPGES-1 的抑制和抗增殖活性的体外评价。
Mol Divers. 2023 Oct;27(5):2185-2215. doi: 10.1007/s11030-022-10551-0. Epub 2022 Nov 4.
3
Extensive Molecular Dynamics Simulations Disclosed the Stability of mPGES-1 Enzyme and the Structural Role of Glutathione (GSH) Cofactor.广泛的分子动力学模拟揭示了 mPGES-1 酶的稳定性和谷胱甘肽 (GSH) 辅因子的结构作用。
Mol Inform. 2022 Dec;41(12):e2200140. doi: 10.1002/minf.202200140. Epub 2022 Sep 29.
4
Sonlicromanol's active metabolite KH176m normalizes prostate cancer stem cell mPGES-1 overexpression and inhibits cancer spheroid growth.超声激活的前列腺癌干细胞 mPGES-1 小分子抑制剂 KH176m 通过抑制前列腺癌细胞球生长抑制肿瘤发生。
PLoS One. 2021 Jul 9;16(7):e0254315. doi: 10.1371/journal.pone.0254315. eCollection 2021.
5
Engineering 'Enzymelink' for screening lead compounds to inhibit mPGES-1 while maintaining prostacyclin synthase activity.工程化“酶连接”筛选抑制 mPGES-1 而同时保持前列环素合酶活性的先导化合物。
Future Med Chem. 2021 Jul;13(13):1091-1103. doi: 10.4155/fmc-2021-0056. Epub 2021 Jun 3.
6
Identification of 2-(thiophen-2-yl)acetic Acid-Based Lead Compound for mPGES-1 Inhibition.用于抑制mPGES-1的基于2-(噻吩-2-基)乙酸的先导化合物的鉴定
Front Chem. 2021 May 7;9:676631. doi: 10.3389/fchem.2021.676631. eCollection 2021.
7
Overview on the Discovery and Development of Anti-Inflammatory Drugs: Should the Focus Be on Synthesis or Degradation of PGE?抗炎药物的发现与开发综述:重点应放在前列腺素E的合成还是降解上?
J Inflamm Res. 2021 Feb 3;14:253-263. doi: 10.2147/JIR.S278514. eCollection 2021.
8
Mechanism of action and potential applications of selective inhibition of microsomal prostaglandin E synthase-1-mediated PGE biosynthesis by sonlicromanol's metabolite KH176m.米索前列醇代谢产物 KH176m 对微粒体前列腺素 E 合酶-1 介导的 PGE 生物合成的选择性抑制作用的作用机制及其潜在应用。
Sci Rep. 2021 Jan 13;11(1):880. doi: 10.1038/s41598-020-79466-w.
9
Targeting mPGES-1 by a Combinatorial Approach: Identification of the Aminobenzothiazole Scaffold to Suppress PGE Levels.通过组合方法靶向微粒体前列腺素E合酶-1:鉴定抑制前列腺素E水平的氨基苯并噻唑支架
ACS Med Chem Lett. 2020 Mar 5;11(5):783-789. doi: 10.1021/acsmedchemlett.9b00618. eCollection 2020 May 14.
10
COX-2-PGE-EPs in gynecological cancers.COX-2-PGE-EPs 在妇科癌症中的作用。
Arch Gynecol Obstet. 2020 Jun;301(6):1365-1375. doi: 10.1007/s00404-020-05559-6. Epub 2020 May 3.

本文引用的文献

1
Microsomal prostaglandin E synthase 1 determines tumor growth in vivo of prostate and lung cancer cells.微粒体前列腺素E合酶1决定前列腺癌细胞和肺癌细胞的体内肿瘤生长。
Proc Natl Acad Sci U S A. 2009 Nov 3;106(44):18757-62. doi: 10.1073/pnas.0910218106. Epub 2009 Oct 21.
2
Microsomal prostaglandin E synthase-1 in both cancer cells and hosts contributes to tumour growth, invasion and metastasis.微粒体前列腺素 E 合酶-1 既存在于癌细胞中,也存在于宿主中,有助于肿瘤的生长、侵袭和转移。
Biochem J. 2009 Dec 23;425(2):361-71. doi: 10.1042/BJ20090045.
3
Immunohistochemical demonstration of membrane-bound prostaglandin E2 synthase-1 in papillary thyroid carcinoma.甲状腺乳头状癌中膜结合型前列腺素E2合酶-1的免疫组化显示
Acta Histochem Cytochem. 2009 Aug 29;42(4):105-9. doi: 10.1267/ahc.09014. Epub 2009 Jul 14.
4
Comparison of microsomal prostaglandin E synthase-1 deletion and COX-2 inhibition in acute cardiac ischemia in mice.比较微小体前列腺素 E 合酶-1 缺失和 COX-2 抑制在小鼠急性心肌缺血中的作用。
Prostaglandins Other Lipid Mediat. 2009 Nov;90(1-2):21-5. doi: 10.1016/j.prostaglandins.2009.06.006. Epub 2009 Jun 25.
5
Microsomal prostaglandin E synthase protein levels correlate with prognosis in colorectal cancer patients.微粒体前列腺素E合酶蛋白水平与结直肠癌患者的预后相关。
Virchows Arch. 2009 Jun;454(6):667-76. doi: 10.1007/s00428-009-0777-z. Epub 2009 May 2.
6
The terminal prostaglandin synthases mPGES-1, mPGES-2, and cPGES are all overexpressed in human gliomas.终末前列腺素合酶mPGES-1、mPGES-2和cPGES在人类胶质瘤中均过度表达。
Neuropathology. 2009 Apr;29(2):156-65. doi: 10.1111/j.1440-1789.2008.00963.x.
7
Pirinixic acid derivatives as novel dual inhibitors of microsomal prostaglandin E2 synthase-1 and 5-lipoxygenase.吡罗昔康酸衍生物作为微粒体前列腺素E2合酶-1和5-脂氧合酶的新型双重抑制剂
J Med Chem. 2008 Dec 25;51(24):8068-76. doi: 10.1021/jm801085s.
8
Cardiovascular events associated with rofecoxib: final analysis of the APPROVe trial.与罗非昔布相关的心血管事件:APPROVe试验的最终分析
Lancet. 2008 Nov 15;372(9651):1756-64. doi: 10.1016/S0140-6736(08)61490-7. Epub 2008 Oct 14.
9
High expression of PGE2 enzymatic pathways in cervical (pre)neoplastic lesions and functional consequences for antigen-presenting cells.PGE2酶促途径在宫颈(癌前)病变中的高表达及其对抗抗原呈递细胞的功能影响
Cancer Immunol Immunother. 2009 Apr;58(4):603-14. doi: 10.1007/s00262-008-0584-4. Epub 2008 Sep 19.
10
Tumor-growth-promoting cyclooxygenase-2 prostaglandin E2 pathway provides medulloblastoma therapeutic targets.促进肿瘤生长的环氧合酶-2前列腺素E2途径提供了髓母细胞瘤的治疗靶点。
Neuro Oncol. 2008 Oct;10(5):661-74. doi: 10.1215/15228517-2008-035. Epub 2008 Aug 20.

mPGES-1 作为癌症抑制的靶点:全面邀请评论“磷脂酶 A2 和脂质介质”。

mPGES-1 as a target for cancer suppression: A comprehensive invited review "Phospholipase A2 and lipid mediators".

机构信息

Center for Molecular Medicine, University of Connecticut Health Center, 263 Farmington Ave., Farmington, CT 06030-3101, USA.

出版信息

Biochimie. 2010 Jun;92(6):660-4. doi: 10.1016/j.biochi.2010.02.006. Epub 2010 Feb 13.

DOI:10.1016/j.biochi.2010.02.006
PMID:20159031
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2898715/
Abstract

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.

摘要

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。