• 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

前列腺素受体信号传导在不同疾病/癌症进展中的作用

Prostanoids receptors signaling in different diseases/cancers progression.

作者信息

Yang Yang, Tang Li-Qin, Wei Wei

机构信息

Institute of Clinical Pharmacology, Anhui Medical University, Hefei, Anhui, People's Republic of China.

出版信息

J Recept Signal Transduct Res. 2013;33(1):14-27. doi: 10.3109/10799893.2012.752003. Epub 2013 Jan 18.

DOI:10.3109/10799893.2012.752003
PMID:23327583
Abstract

Prostanoids, that is, prostaglandins (PGs) PGE(2), PGF(2α), PGI(2), PGD(2) and thromboxane A(2)(TXA(2)), are the oldest members of the eicosanoid family. The PGs are a family of lipid mediators formed in response to various stimuli. They are transported into the extracellular microenvironment by specific multidrug resistance-associated proteins (MRPs) after synthesis. Once exported to the microenvironment, prostanoids bind to G-protein coupled receptors that contain seven transmembrane spanning domains. There are eight types of the prostanoid receptors conserved in mammals from mouse to human. They are the PGD receptor (DP), four subtypes of the PGE receptor (EP(1), EP(2), EP(3) and EP(4)), the PGF receptor (FP), PGI receptor (IP) and TXA receptor (TP). Recently, several studies have revealed the roles of PG receptor signaling in various pathological conditions, and suggest that selective manipulation of the prostanoid receptors may be beneficial in treatment of the pathological conditions. Here we review these recent findings of roles of prostanoid receptor signaling and their therapeutic implications.

摘要

前列腺素类物质,即前列腺素(PGs)PGE(2)、PGF(2α)、PGI(2)、PGD(2)和血栓素A(2)(TXA(2)),是类花生酸家族中最古老的成员。前列腺素是一类脂质介质,在各种刺激下形成。它们在合成后通过特定的多药耐药相关蛋白(MRPs)转运到细胞外微环境中。一旦分泌到微环境中,前列腺素类物质就会与含有七个跨膜结构域的G蛋白偶联受体结合。在从小鼠到人类的哺乳动物中,存在八种保守的前列腺素类受体。它们是前列腺素D受体(DP)、前列腺素E受体的四种亚型(EP(1)、EP(2)、EP(3)和EP(4))、前列腺素F受体(FP)、前列腺素I受体(IP)和血栓素A受体(TP)。最近,多项研究揭示了前列腺素受体信号在各种病理状况中的作用,并表明对前列腺素类受体进行选择性调控可能对治疗这些病理状况有益。在此,我们综述前列腺素类受体信号作用的这些最新发现及其治疗意义。

相似文献

1
Prostanoids receptors signaling in different diseases/cancers progression.前列腺素受体信号传导在不同疾病/癌症进展中的作用
J Recept Signal Transduct Res. 2013;33(1):14-27. doi: 10.3109/10799893.2012.752003. Epub 2013 Jan 18.
2
Prostaglandin receptor signaling in disease.疾病中的前列腺素受体信号传导
ScientificWorldJournal. 2007 Sep 1;7:1329-47. doi: 10.1100/tsw.2007.182.
3
Prostanoid receptors: subtypes and signaling.前列腺素受体:亚型与信号传导
Annu Rev Pharmacol Toxicol. 2001;41:661-90. doi: 10.1146/annurev.pharmtox.41.1.661.
4
Prostaglandins in the kidney: developments since Y2K.肾脏中的前列腺素:自千禧年以来的进展。
Clin Sci (Lond). 2007 Oct;113(7):297-311. doi: 10.1042/CS20070089.
5
Roles of prostanoids in the pathogenesis of cardiovascular diseases: Novel insights from knockout mouse studies.前列腺素在心血管疾病发病机制中的作用:来自基因敲除小鼠研究的新见解。
Pharmacol Ther. 2011 Feb;129(2):195-205. doi: 10.1016/j.pharmthera.2010.09.004.
6
Prostanoid receptor assays.前列腺素受体测定
Curr Protoc Pharmacol. 2001 Nov;Chapter 4:Unit4.18. doi: 10.1002/0471141755.ph0418s14.
7
Prostanoids and prostanoid receptors in signal transduction.信号转导中的前列腺素和前列腺素受体
Int J Biochem Cell Biol. 2004 Jul;36(7):1187-205. doi: 10.1016/j.biocel.2003.08.006.
8
Function of prostanoid receptors: studies on knockout mice.前列腺素受体的功能:基因敲除小鼠研究
Prostaglandins Other Lipid Mediat. 2002 Aug;68-69:557-73. doi: 10.1016/s0090-6980(02)00055-2.
9
Modulation of norepinephrine release from sympathetic neurons of the rabbit aorta by prejunctional prostanoid receptors.前膜前列腺素受体对兔主动脉交感神经元去甲肾上腺素释放的调节作用。
J Pharmacol Exp Ther. 1999 Oct;291(1):7-11.
10
Thromboxane A2 and prostaglandin F2alpha mediate inflammatory tachycardia.血栓素A2和前列腺素F2α介导炎症性心动过速。
Nat Med. 2005 May;11(5):562-6. doi: 10.1038/nm1231. Epub 2005 Apr 17.

引用本文的文献

1
Activity-dependent COX-2 proteolysis modulates aerobic respiration and proliferation in a prostaglandin-independent manner.活性依赖的COX-2蛋白水解以不依赖前列腺素的方式调节有氧呼吸和增殖。
iScience. 2024 Nov 17;27(12):111403. doi: 10.1016/j.isci.2024.111403. eCollection 2024 Dec 20.
2
Liquid chromatography coupled to high-resolution mass spectrometry metabolomics: A useful tool for investigating tumor secretome based on a three-dimensional co-culture model.液相色谱-高分辨质谱代谢组学:一种基于三维共培养模型研究肿瘤分泌组的有用工具。
PLoS One. 2022 Sep 21;17(9):e0274623. doi: 10.1371/journal.pone.0274623. eCollection 2022.
3
Development of Fluorescence Imaging Probes for Labeling COX-1 in Live Ovarian Cancer Cells.
用于标记活卵巢癌细胞中COX-1的荧光成像探针的研发
ACS Med Chem Lett. 2021 Apr 8;12(5):798-804. doi: 10.1021/acsmedchemlett.1c00065. eCollection 2021 May 13.
4
Limited Proteolysis of Cyclooxygenase-2 Enhances Cell Proliferation.环氧化酶-2 的有限蛋白水解增强细胞增殖。
Int J Mol Sci. 2020 Apr 30;21(9):3195. doi: 10.3390/ijms21093195.
5
Toll-Like Receptor 4 (TLR4)/Cyclooxygenase-2 (COX-2) Regulates Prostate Cancer Cell Proliferation, Migration, and Invasion by NF-κB Activation.Toll 样受体 4(TLR4)/环氧化酶-2(COX-2)通过 NF-κB 激活调节前列腺癌细胞增殖、迁移和侵袭。
Med Sci Monit. 2018 Aug 11;24:5588-5597. doi: 10.12659/MSM.906857.
6
Prostaglandin signaling regulates nephron segment patterning of renal progenitors during zebrafish kidney development.前列腺素信号传导在斑马鱼肾脏发育过程中调节肾祖细胞的肾单位节段模式。
Elife. 2016 Dec 20;5:e17551. doi: 10.7554/eLife.17551.
7
Renoprotective effect of berberine via regulating the PGE2 -EP1-Gαq-Ca(2+) signalling pathway in glomerular mesangial cells of diabetic rats.黄连素通过调节糖尿病大鼠肾小球系膜细胞中PGE2 -EP1-Gαq-Ca(2+)信号通路发挥肾脏保护作用。
J Cell Mol Med. 2016 Aug;20(8):1491-502. doi: 10.1111/jcmm.12837. Epub 2016 Apr 21.
8
Inhibition of Prostaglandin Reductase 2, a Putative Oncogene Overexpressed in Human Pancreatic Adenocarcinoma, Induces Oxidative Stress-Mediated Cell Death Involving xCT and CTH Gene Expressions through 15-Keto-PGE2.抑制前列腺素还原酶2(一种在人胰腺腺癌中过表达的假定癌基因)通过15-酮基前列腺素E2诱导涉及xCT和CTH基因表达的氧化应激介导的细胞死亡。
PLoS One. 2016 Jan 28;11(1):e0147390. doi: 10.1371/journal.pone.0147390. eCollection 2016.
9
A Double Whammy: Targeting Both Fatty Acid Amide Hydrolase (FAAH) and Cyclooxygenase (COX) To Treat Pain and Inflammation.双重打击:靶向脂肪酸酰胺水解酶(FAAH)和环氧化酶(COX)治疗疼痛和炎症。
ChemMedChem. 2016 Jun 20;11(12):1242-51. doi: 10.1002/cmdc.201500395. Epub 2015 Oct 21.
10
Bone and skeletal muscle: Key players in mechanotransduction and potential overlapping mechanisms.骨骼与骨骼肌:机械转导中的关键参与者及潜在的重叠机制
Bone. 2015 Nov;80:24-36. doi: 10.1016/j.bone.2015.04.014.