• 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

细胞程序性坏死:一种新兴的细胞死亡方式。

Necroptosis: an emerging form of programmed cell death.

机构信息

Department of Hematology, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Rd, Nanjing 210029, PR China.

出版信息

Crit Rev Oncol Hematol. 2012 Jun;82(3):249-58. doi: 10.1016/j.critrevonc.2011.08.004. Epub 2011 Oct 1.

DOI:10.1016/j.critrevonc.2011.08.004
PMID:21962882
Abstract

Necrosis plays an important role in multiple physiological and pathological processes. Recently, a relatively new form of necrosis has been characterized as "necroptosis". Morphologically, necroptosis exhibits the features of necrosis; however, necroptosis exhibits a unique signaling pathway that requires the involvement of receptor interaction protein kinase 1 and 3 (RIP1 and RIP3) and can be specifically inhibited by necrostatins. Necroptosis has been found to contribute to the regulation of immune system, cancer development as well as cellular responses to multiple stresses. In this review, we will summarize the signaling pathway, biological effects and pathological significance of this specific form of programmed cell death.

摘要

细胞坏死在多种生理和病理过程中发挥着重要作用。最近,一种相对较新的细胞坏死形式被定义为“细胞坏死性凋亡”。在形态学上,细胞坏死性凋亡表现出坏死的特征;然而,细胞坏死性凋亡具有独特的信号通路,需要受体相互作用蛋白激酶 1 和 3(RIP1 和 RIP3)的参与,并且可以被特异性的坏死抑制剂所抑制。细胞坏死性凋亡被发现参与免疫系统的调节、癌症的发展以及细胞对多种应激的反应。在这篇综述中,我们将总结这种特定形式的程序性细胞死亡的信号通路、生物学效应和病理意义。

相似文献

1
Necroptosis: an emerging form of programmed cell death.细胞程序性坏死:一种新兴的细胞死亡方式。
Crit Rev Oncol Hematol. 2012 Jun;82(3):249-58. doi: 10.1016/j.critrevonc.2011.08.004. Epub 2011 Oct 1.
2
Cytosolic calcium mediates RIP1/RIP3 complex-dependent necroptosis through JNK activation and mitochondrial ROS production in human colon cancer cells.胞质钙通过激活JNK和产生活线粒体ROS介导人结肠癌细胞中RIP1/RIP3复合物依赖性坏死性凋亡。
Free Radic Biol Med. 2017 Jul;108:433-444. doi: 10.1016/j.freeradbiomed.2017.04.010. Epub 2017 Apr 14.
3
β-Lapachone induces programmed necrosis through the RIP1-PARP-AIF-dependent pathway in human hepatocellular carcinoma SK-Hep1 cells.β-拉帕醌通过RIP1-PARP-AIF依赖性途径诱导人肝癌SK-Hep1细胞发生程序性坏死。
Cell Death Dis. 2014 May 15;5(5):e1230. doi: 10.1038/cddis.2014.202.
4
RIP1/RIP3-regulated necroptosis as a target for multifaceted disease therapy (Review).RIP1/RIP3 调节的坏死性凋亡作为多方面疾病治疗的靶点(综述)。
Int J Mol Med. 2019 Sep;44(3):771-786. doi: 10.3892/ijmm.2019.4244. Epub 2019 Jun 14.
5
Connections between various trigger factors and the RIP1/ RIP3 signaling pathway involved in necroptosis.各种触发因素与坏死性凋亡中涉及的RIP1/RIP3信号通路之间的联系。
Asian Pac J Cancer Prev. 2013;14(12):7069-74. doi: 10.7314/apjcp.2013.14.12.7069.
6
Smac mimetic triggers necroptosis in pancreatic carcinoma cells when caspase activation is blocked.当半胱天冬酶激活被阻断时,Smac模拟物可触发胰腺癌细胞发生坏死性凋亡。
Cancer Lett. 2016 Sep 28;380(1):31-8. doi: 10.1016/j.canlet.2016.05.036. Epub 2016 Jun 3.
7
Emodin induced necroptosis in the glioma cell line U251 via the TNF-α/RIP1/RIP3 pathway.大黄素通过 TNF-α/RIP1/RIP3 通路诱导脑胶质瘤 U251 细胞发生坏死性凋亡。
Invest New Drugs. 2020 Feb;38(1):50-59. doi: 10.1007/s10637-019-00764-w. Epub 2019 Mar 28.
8
CD40 ligand induces RIP1-dependent, necroptosis-like cell death in low-grade serous but not serous borderline ovarian tumor cells.CD40配体在低度浆液性卵巢肿瘤细胞中诱导依赖RIP1的、坏死性凋亡样细胞死亡,但在浆液性交界性卵巢肿瘤细胞中则不然。
Cell Death Dis. 2015 Aug 27;6(8):e1864. doi: 10.1038/cddis.2015.229.
9
Shikonin induces glioma cell necroptosis in vitro by ROS overproduction and promoting RIP1/RIP3 necrosome formation.紫草素通过过量产生活性氧和促进RIP1/RIP3坏死小体形成在体外诱导胶质瘤细胞坏死性凋亡。
Acta Pharmacol Sin. 2017 Nov;38(11):1543-1553. doi: 10.1038/aps.2017.112. Epub 2017 Aug 17.
10
ARHI (DIRAS3)-mediated autophagy-associated cell death enhances chemosensitivity to cisplatin in ovarian cancer cell lines and xenografts.ARHI(DIRAS3)介导的自噬相关细胞死亡增强了卵巢癌细胞系和异种移植瘤对顺铂的化疗敏感性。
Cell Death Dis. 2015 Aug 6;6(8):e1836. doi: 10.1038/cddis.2015.208.

引用本文的文献

1
The OvarianTag™ Biomarker Panel Emerges as a Prognostic Tool to Guide Clinical Decisions in Cisplatin-Based Treatment of Epithelial Ovarian Cancer.OvarianTag™生物标志物组合成为一种预后工具,可指导基于顺铂的上皮性卵巢癌治疗中的临床决策。
Int J Mol Sci. 2025 Aug 29;26(17):8393. doi: 10.3390/ijms26178393.
2
Reactive Oxygen Species: A Double-Edged Sword in the Modulation of Cancer Signaling Pathway Dynamics.活性氧:癌症信号通路动力学调控中的双刃剑
Cells. 2025 Aug 6;14(15):1207. doi: 10.3390/cells14151207.
3
Exploring necroptosis: mechanistic analysis and antitumor potential of nanomaterials.
探索坏死性凋亡:纳米材料的机制分析及其抗肿瘤潜力
Cell Death Discov. 2025 Apr 29;11(1):211. doi: 10.1038/s41420-025-02423-x.
4
Beclin-1: a therapeutic target at the intersection of autophagy, immunotherapy, and cancer treatment.贝林1:自噬、免疫疗法与癌症治疗交叉领域的一个治疗靶点
Front Immunol. 2024 Nov 22;15:1506426. doi: 10.3389/fimmu.2024.1506426. eCollection 2024.
5
Targeting regulated cell death pathways in cancers for effective treatment: a comprehensive review.靶向癌症中受调控的细胞死亡途径以实现有效治疗:全面综述
Front Cell Dev Biol. 2024 Nov 15;12:1462339. doi: 10.3389/fcell.2024.1462339. eCollection 2024.
6
Cyclophosphamide induces ovarian granulosa cell ferroptosis via a mechanism associated with HO-1 and ROS-mediated mitochondrial dysfunction.环磷酰胺通过与 HO-1 和 ROS 介导的线粒体功能障碍相关的机制诱导卵巢颗粒细胞发生铁死亡。
J Ovarian Res. 2024 May 18;17(1):107. doi: 10.1186/s13048-024-01434-z.
7
Metabolic changes enhance necroptosis of type 2 diabetes mellitus mice infected with Mycobacterium tuberculosis.代谢变化增强了感染结核分枝杆菌的 2 型糖尿病小鼠的坏死性凋亡。
PLoS Pathog. 2024 May 10;20(5):e1012148. doi: 10.1371/journal.ppat.1012148. eCollection 2024 May.
8
Frontier knowledge and future directions of programmed cell death in clear cell renal cell carcinoma.透明细胞肾细胞癌中程序性细胞死亡的前沿知识与未来方向
Cell Death Discov. 2024 Mar 5;10(1):113. doi: 10.1038/s41420-024-01880-0.
9
IE1 of Human Cytomegalovirus Inhibits Necroptotic Cell Death via Direct and Indirect Modulation of the Necrosome Complex.人巨细胞病毒 IE1 通过直接和间接调节坏死小体复合物抑制细胞坏死性死亡。
Viruses. 2024 Feb 13;16(2):290. doi: 10.3390/v16020290.
10
vaccination caused by diverse irradiation-driven cell death programs.多种辐射驱动的细胞死亡程序引起的接种。
Theranostics. 2024 Jan 12;14(3):1147-1167. doi: 10.7150/thno.86004. eCollection 2024.