• 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

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?

Apoptosis, necroptosis, and pyroptosis as alternative cell death pathways induced by chemotherapeutic agents?

机构信息

University of Lodz, Faculty of Biology and Environmental Protection, Department of Molecular Biotechnology and Genetics, Banacha St. 12/16, 90-237 Lodz, Poland; University of Lodz, Doctoral School of Exact and Natural Sciences, Banacha Street 12/16, 90-237 Lodz, Poland.

University of Lodz, Faculty of Biology and Environmental Protection, Department of Molecular Biotechnology and Genetics, Banacha St. 12/16, 90-237 Lodz, Poland.

出版信息

Biochim Biophys Acta Rev Cancer. 2023 Nov;1878(6):189024. doi: 10.1016/j.bbcan.2023.189024. Epub 2023 Nov 18.

DOI:10.1016/j.bbcan.2023.189024
PMID:37980943
Abstract

For decades, common chemotherapeutic drugs have been established to trigger apoptosis, the preferred immunologically "silent" form of cell death. The primary objective of this review was to show that various FDA-approved chemotherapeutic drugs, including cisplatin, cyclosporine, doxorubicin, etoposide, 5-fluorouracil, gemcitabine, paclitaxel, or vinblastine can trigger necroptosis and pyroptosis. We aimed to provide the advantages and disadvantages of the induction of the given type of cell death by chemotherapeutical agents. Moreover, we give a short overview of the molecular mechanism of each type of cell death and indicate the existing crosstalks between cell death types. Finally, we provide a comparison of cell death types to facilitate the exploration of cell death types induced by other chemotherapeutical agents. Understanding the cell death pathway induced by a drug can lessen side effects and assist the discovery of new combinations with synergistic effects and low systemic toxicity.

摘要

几十年来,已确立常用的化疗药物来触发细胞凋亡,这是首选的免疫“沉默”形式的细胞死亡。本综述的主要目的是表明,各种已批准的 FDA 化疗药物,包括顺铂、环孢素、阿霉素、依托泊苷、5-氟尿嘧啶、吉西他滨、紫杉醇或长春碱,可触发细胞坏死和细胞焦亡。我们旨在提供化疗药物诱导给定类型细胞死亡的优缺点。此外,我们简要概述了每种类型细胞死亡的分子机制,并指出了细胞死亡类型之间的现有串扰。最后,我们比较了细胞死亡类型,以促进探索其他化疗药物诱导的细胞死亡类型。了解药物诱导的细胞死亡途径可以减少副作用,并有助于发现具有协同作用和低全身毒性的新组合。

相似文献

1
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.
2
New insights into the regulation of apoptosis, necroptosis, and pyroptosis by receptor interacting protein kinase 1 and caspase-8.受体相互作用蛋白激酶 1 和半胱天冬酶-8 调控细胞凋亡、坏死性凋亡和细胞焦亡的新见解。
Curr Opin Cell Biol. 2020 Apr;63:186-193. doi: 10.1016/j.ceb.2020.02.004. Epub 2020 Mar 9.
3
Targeting cell death pathways for cancer therapy: recent developments in necroptosis, pyroptosis, ferroptosis, and cuproptosis research.针对癌症治疗的细胞死亡途径:细胞坏死、细胞焦亡、铁死亡和铜死亡研究的新进展。
J Hematol Oncol. 2022 Dec 8;15(1):174. doi: 10.1186/s13045-022-01392-3.
4
Inflammatory cell death: how macrophages sense neighbouring cell infection and damage.炎症细胞死亡:巨噬细胞如何感知邻近细胞的感染和损伤。
Biochem Soc Trans. 2023 Feb 27;51(1):303-313. doi: 10.1042/BST20220807.
5
Ferroptosis, necroptosis, and pyroptosis in cancer: Crucial cell death types in radiotherapy and post-radiotherapy immune activation.铁死亡、坏死性凋亡和细胞焦亡在癌症中的作用:放疗及放疗后免疫激活中的关键细胞死亡类型。
Radiother Oncol. 2023 Jul;184:109689. doi: 10.1016/j.radonc.2023.109689. Epub 2023 May 6.
6
Apoptosis, Pyroptosis, and Necroptosis-Oh My! The Many Ways a Cell Can Die.凋亡、焦亡和坏死性凋亡——天哪!细胞死亡的多种方式。
J Mol Biol. 2022 Feb 28;434(4):167378. doi: 10.1016/j.jmb.2021.167378. Epub 2021 Nov 25.
7
Viral manipulation of host cell necroptosis and pyroptosis.病毒对宿主细胞坏死性凋亡和细胞焦亡的影响。
Trends Microbiol. 2022 Jun;30(6):593-605. doi: 10.1016/j.tim.2021.11.011. Epub 2021 Dec 18.
8
The scheme, and regulative mechanism of pyroptosis, ferroptosis, and necroptosis in radiation injury.辐射损伤中细胞焦亡、铁死亡和坏死性凋亡的发生机制及调控。
Int J Biol Sci. 2024 Mar 3;20(5):1871-1883. doi: 10.7150/ijbs.91112. eCollection 2024.
9
Deciphering the Molecular Nexus: An In-Depth Review of Mitochondrial Pathways and Their Role in Cell Death Crosstalk.解析分子关联:线粒体途径及其在细胞死亡串扰中的作用的深入综述。
Cells. 2024 May 17;13(10):863. doi: 10.3390/cells13100863.
10
From pyroptosis, apoptosis and necroptosis to PANoptosis: A mechanistic compendium of programmed cell death pathways.从焦亡、凋亡和坏死性凋亡到PANoptosis:程序性细胞死亡途径的机制综述
Comput Struct Biotechnol J. 2021 Aug 3;19:4641-4657. doi: 10.1016/j.csbj.2021.07.038. eCollection 2021.

引用本文的文献

1
Long non-coding RNA STMN1P2 promotes breast cancer doxorubicin resistance by inhibiting pyroptosis through the hnRNPU-EZH2-TARF6-MALT1-caspase-1 pathway.长链非编码RNA STMN1P2通过hnRNPU-EZH2-TARF6-MALT1-半胱天冬酶-1途径抑制细胞焦亡,从而促进乳腺癌对阿霉素的耐药性。
Acta Pharmacol Sin. 2025 Sep 8. doi: 10.1038/s41401-025-01653-0.
2
Construction and immunohistochemical validation of a necroptosis-related prognostic signature in bladder cancer and its association with tumor immune infiltration.膀胱癌中坏死性凋亡相关预后标志物的构建、免疫组化验证及其与肿瘤免疫浸润的关联
Front Genet. 2025 Aug 14;16:1527907. doi: 10.3389/fgene.2025.1527907. eCollection 2025.
3
PEPAD: A Promising Therapeutic Approach for the Treatment of Murine Melanoma (B16F10-Nex2).
PEPAD:一种治疗小鼠黑色素瘤(B16F10-Nex2)的有前景的治疗方法。
Pharmaceuticals (Basel). 2025 Aug 14;18(8):1203. doi: 10.3390/ph18081203.
4
Pentoxifylline Enhances the Effects of Doxorubicin and Bleomycin on Apoptosis, Caspase Activity, and Cell Cycle While Reducing Proliferation and Senescence in Hodgkin's Disease Cell Line.己酮可可碱增强阿霉素和博来霉素对霍奇金病细胞系凋亡、半胱天冬酶活性及细胞周期的影响,同时降低其增殖和衰老。
Curr Issues Mol Biol. 2025 Jul 28;47(8):593. doi: 10.3390/cimb47080593.
5
Advances in cold atmospheric plasma therapy for cancer.冷大气等离子体癌症治疗的进展
Bioact Mater. 2025 Jul 25;53:433-458. doi: 10.1016/j.bioactmat.2025.07.031. eCollection 2025 Nov.
6
Adrenocortical carcinoma survival gene HMMR was identified as being targeted by fluorouracil and epirubicin using a gene coexpression network-based drug repositioning strategy.使用基于基因共表达网络的药物重新定位策略,肾上腺皮质癌生存基因HMMR被确定为氟尿嘧啶和表柔比星的作用靶点。
Sci Rep. 2025 Jul 17;15(1):25912. doi: 10.1038/s41598-025-10452-w.
7
Phosphorylated IRF3 promotes GSDME-mediated pyroptosis through RIPK1/FADD/caspase-8 complex formation during mitotic arrest in ovarian cancer.在卵巢癌有丝分裂停滞期间,磷酸化的IRF3通过RIPK1/FADD/半胱天冬酶-8复合物的形成促进GSDME介导的细胞焦亡。
Cell Commun Signal. 2025 Jul 1;23(1):306. doi: 10.1186/s12964-025-02322-9.
8
Functionalization-Dependent Cytotoxicity of Silver Nanoparticles: A Comparative Study of Chlorhexidine and Metronidazole Conjugates.银纳米颗粒功能化依赖性细胞毒性:洗必泰和甲硝唑共轭物的比较研究
Biomolecules. 2025 Jun 10;15(6):850. doi: 10.3390/biom15060850.
9
Caffeic Acid Phenethyl Ester Protects Against Doxorubicin-Induced Cardiotoxicity via Inhibiting the ROS-MLKL-Mediated Cross-Talk Between Oxidative Stress and Necroptosis.咖啡酸苯乙酯通过抑制ROS-MLKL介导的氧化应激与坏死性凋亡之间的相互作用来预防阿霉素诱导的心脏毒性。
Biomolecules. 2025 May 28;15(6):783. doi: 10.3390/biom15060783.
10
Dibromo-Edaravone Induces Anti-Erythroleukemia Effects via the JAK2-STAT3 Signaling Pathway.二溴依达拉奉通过JAK2-STAT3信号通路诱导抗红白血病作用。
Int J Mol Sci. 2025 Apr 23;26(9):4000. doi: 10.3390/ijms26094000.