• 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

死亡受体5的研究进展

Advances in the study of death receptor 5.

作者信息

Qiao Xuan, Guo Shuang, Meng Zhiyun, Gan Hui, Wu Zhuona, Sun Yunbo, Liu Shuchen, Dou Guifang, Gu Ruolan

机构信息

Graduate Collaborative Training Base of Academy of Military Medical Sciences, Hengyang Medical School, University of South China, Hengyang, China.

Beijing Institute of Radiation Medicine, Beijing, China.

出版信息

Front Pharmacol. 2025 Mar 12;16:1549808. doi: 10.3389/fphar.2025.1549808. eCollection 2025.

DOI:10.3389/fphar.2025.1549808
PMID:40144653
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11936945/
Abstract

DR5, a receptor with the highest affinity for TRAIL under physiological conditions, selectively induces apoptosis in specific target cells such as tumor and aberrant immune cells, while minimally affecting normal cells. The TRAIL-DR5 signaling pathway is a crucial regulatory mechanism when the body responds to various exogenous interference factors, including viruses, chemicals, and radiation. This pathway plays a vital role in maintaining physiological homeostasis and in the pathological development of various diseases. Different modulations of DR5, such as upregulation, activation, and antagonism, hold significant potential for therapeutic applications in tumors, cardiovascular diseases, autoimmune diseases, viral infections, and radiation injuries. This article provides an overview of the current research progress on DR5, including the status and prospects of its clinical applications.

摘要

DR5是在生理条件下对TRAIL具有最高亲和力的受体,可选择性地诱导肿瘤和异常免疫细胞等特定靶细胞凋亡,同时对正常细胞影响极小。TRAIL-DR5信号通路是机体对包括病毒、化学物质和辐射在内的各种外源性干扰因素作出反应时的关键调节机制。该通路在维持生理稳态以及各种疾病的病理发展中起着至关重要的作用。对DR5的不同调节,如上调、激活和拮抗,在肿瘤、心血管疾病、自身免疫性疾病、病毒感染和辐射损伤的治疗应用中具有巨大潜力。本文概述了DR5的当前研究进展,包括其临床应用的现状和前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a90c/11936945/65072b6a2e60/fphar-16-1549808-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a90c/11936945/8cb1135870d9/fphar-16-1549808-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a90c/11936945/65072b6a2e60/fphar-16-1549808-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a90c/11936945/8cb1135870d9/fphar-16-1549808-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a90c/11936945/65072b6a2e60/fphar-16-1549808-g002.jpg

相似文献

1
Advances in the study of death receptor 5.死亡受体5的研究进展
Front Pharmacol. 2025 Mar 12;16:1549808. doi: 10.3389/fphar.2025.1549808. eCollection 2025.
2
Tumor necrosis factor-related apoptosis-inducing ligand-mediated apoptosis in established and primary glioma cell lines.肿瘤坏死因子相关凋亡诱导配体介导的已建立和原发性胶质瘤细胞系中的细胞凋亡
Neurosurg Focus. 2002 Sep 15;13(3):ecp1. doi: 10.3171/foc.2002.13.3.6.
3
Blocking TRAIL-DR5 signaling pathway with soluble death receptor 5 fusion protein mitigates radiation-induced injury.用可溶性死亡受体5融合蛋白阻断TRAIL-DR5信号通路可减轻辐射诱导的损伤。
Front Pharmacol. 2023 May 18;14:1171293. doi: 10.3389/fphar.2023.1171293. eCollection 2023.
4
Death receptor 5 contributes to cardiomyocyte hypertrophy through epidermal growth factor receptor transactivation.死亡受体 5 通过表皮生长因子受体的转激活促进心肌细胞肥大。
J Mol Cell Cardiol. 2019 Nov;136:1-14. doi: 10.1016/j.yjmcc.2019.08.011. Epub 2019 Aug 29.
5
Targeting Death Receptor 5 (DR5) for the imaging and treatment of primary bone and soft tissue tumors: an update of the literature.靶向死亡受体5(DR5)用于原发性骨与软组织肿瘤的成像及治疗:文献综述
Front Mol Biosci. 2024 Sep 2;11:1384795. doi: 10.3389/fmolb.2024.1384795. eCollection 2024.
6
Quinacrine induces apoptosis in cancer cells by forming a functional bridge between TRAIL-DR5 complex and modulating the mitochondrial intrinsic cascade.喹吖因通过在肿瘤坏死因子相关凋亡诱导配体(TRAIL)-死亡受体5(DR5)复合物之间形成功能性桥梁并调节线粒体内在凋亡级联反应来诱导癌细胞凋亡。
Oncotarget. 2017 Jan 3;8(1):248-267. doi: 10.18632/oncotarget.11335.
7
TRAIL induces apoptosis but not necroptosis in colorectal and pancreatic cancer cells preferentially via the TRAIL-R2/DR5 receptor.TRAIL 通过 TRAIL-R2/DR5 受体优先诱导结直肠和胰腺癌细胞凋亡而不是坏死。
Biochim Biophys Acta Mol Cell Res. 2018 Mar;1865(3):522-531. doi: 10.1016/j.bbamcr.2017.12.006. Epub 2017 Dec 24.
8
Selective TRAIL-triggered apoptosis due to overexpression of TRAIL death receptor 5 (DR5) in P-glycoprotein-bearing multidrug resistant CEM/VBL1000 human leukemia cells.在表达P-糖蛋白的多药耐药CEM/VBL1000人白血病细胞中,由于TRAIL死亡受体5(DR5)的过表达导致的选择性TRAIL触发的细胞凋亡。
Int J Biochem Mol Biol. 2010;1(1):90-100. Epub 2010 Jul 18.
9
Histone deacetylase inhibitors upregulate death receptor 5/TRAIL-R2 and sensitize apoptosis induced by TRAIL/APO2-L in human malignant tumor cells.组蛋白去乙酰化酶抑制剂上调死亡受体5/TRAIL-R2,并使人类恶性肿瘤细胞对TRAIL/APO2-L诱导的凋亡敏感。
Oncogene. 2004 Aug 19;23(37):6261-71. doi: 10.1038/sj.onc.1207830.
10
Ewing's sarcoma family tumors are sensitive to tumor necrosis factor-related apoptosis-inducing ligand and express death receptor 4 and death receptor 5.尤因肉瘤家族性肿瘤对肿瘤坏死因子相关凋亡诱导配体敏感,并表达死亡受体4和死亡受体5。
Cancer Res. 2001 Mar 15;61(6):2704-12.

引用本文的文献

1
Engineering hybrid nanoparticles for targeted codelivery of triptolide and -siRNA against pulmonary metastatic melanoma.工程化杂合纳米颗粒用于雷公藤甲素和-siRNA的靶向共递送以对抗肺转移性黑色素瘤。
Sci Adv. 2025 Jul 25;11(30):eadv6990. doi: 10.1126/sciadv.adv6990. Epub 2025 Jul 23.

本文引用的文献

1
An antibiotic that mediates immune destruction of senescent cancer cells.一种介导衰老癌细胞免疫破坏的抗生素。
Proc Natl Acad Sci U S A. 2024 Dec 24;121(52):e2417724121. doi: 10.1073/pnas.2417724121. Epub 2024 Dec 18.
2
Combination of multivalent DR5 receptor clustering agonists and histone deacetylase inhibitors for treatment of colon cancer.多价DR5受体聚集激动剂与组蛋白去乙酰化酶抑制剂联合用于治疗结肠癌。
J Control Release. 2024 Dec;376:1014-1024. doi: 10.1016/j.jconrel.2024.10.062. Epub 2024 Nov 8.
3
Targeting Death Receptor 5 (DR5) for the imaging and treatment of primary bone and soft tissue tumors: an update of the literature.
靶向死亡受体5(DR5)用于原发性骨与软组织肿瘤的成像及治疗:文献综述
Front Mol Biosci. 2024 Sep 2;11:1384795. doi: 10.3389/fmolb.2024.1384795. eCollection 2024.
4
Blocking the TRAIL-DR5 Pathway Reduces Cardiac Ischemia-Reperfusion Injury by Decreasing Neutrophil Infiltration and Neutrophil Extracellular Traps Formation.阻断TRAIL-DR5信号通路可通过减少中性粒细胞浸润和中性粒细胞胞外诱捕网形成来减轻心脏缺血再灌注损伤。
Cardiovasc Drugs Ther. 2024 Jun 20. doi: 10.1007/s10557-024-07591-z.
5
Death receptor 5 is required for intestinal stem cell activity during intestinal epithelial renewal at homoeostasis.死亡受体 5 在肠道上皮细胞更新的肠稳态过程中对于肠道干细胞活性是必需的。
Cell Death Dis. 2024 Jan 10;15(1):27. doi: 10.1038/s41419-023-06409-4.
6
Programmed death of macrophages in atherosclerosis: mechanisms and therapeutic targets.动脉粥样硬化中巨噬细胞的程序性死亡:机制与治疗靶点。
Nat Rev Cardiol. 2024 May;21(5):312-325. doi: 10.1038/s41569-023-00957-0. Epub 2024 Jan 2.
7
A guide to cell death pathways.细胞死亡途径指南。
Nat Rev Mol Cell Biol. 2024 May;25(5):379-395. doi: 10.1038/s41580-023-00689-6. Epub 2023 Dec 18.
8
Apoptosis, necroptosis, and pyroptosis as alternative cell death pathways induced by chemotherapeutic agents?化疗药物诱导的细胞凋亡、坏死性凋亡和细胞焦亡:细胞死亡的另一种途径?
Biochim Biophys Acta Rev Cancer. 2023 Nov;1878(6):189024. doi: 10.1016/j.bbcan.2023.189024. Epub 2023 Nov 18.
9
Anti-tumor activity of 5-aminoimidazole-4-carboxamide riboside with AMPK-independent cell death in human adult T-cell leukemia/lymphoma.5-氨基咪唑-4-甲酰胺核苷在人成人T细胞白血病/淋巴瘤中通过不依赖AMPK的细胞死亡发挥抗肿瘤活性。
Eur J Pharmacol. 2023 Dec 15;961:176180. doi: 10.1016/j.ejphar.2023.176180. Epub 2023 Nov 11.
10
After cell death: the molecular machinery of efferocytosis.细胞死亡后:噬细胞作用的分子机制。
Exp Mol Med. 2023 Aug;55(8):1644-1651. doi: 10.1038/s12276-023-01070-5. Epub 2023 Aug 23.