• 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

凋亡逃避作为癌症中的一种细胞应激反应

Evasion of apoptosis as a cellular stress response in cancer.

作者信息

Fulda Simone

机构信息

Ulm University, Children's Hospital, Eythstrasse 24, 89075 Ulm, Germany.

出版信息

Int J Cell Biol. 2010;2010:370835. doi: 10.1155/2010/370835. Epub 2010 Feb 18.

DOI:10.1155/2010/370835
PMID:20182539
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2825553/
Abstract

One of the hallmarks of human cancers is the intrinsic or acquired resistance to apoptosis. Evasion of apoptosis can be part of a cellular stress response to ensure the cell's survival upon exposure to stressful stimuli. Apoptosis resistance may contribute to carcinogenesis, tumor progression, and also treatment resistance, since most current anticancer therapies including chemotherapy as well as radio- and immunotherapies primarily act by activating cell death pathways including apoptosis in cancer cells. Hence, a better understanding of the molecular mechanisms regarding how cellular stress stimuli trigger antiapoptotic mechanisms and how this contributes to tumor resistance to apoptotic cell death is expected to provide the basis for a rational approach to overcome apoptosis resistance mechanisms in cancers.

摘要

人类癌症的一个标志是对细胞凋亡具有内在或获得性抗性。逃避细胞凋亡可能是细胞应激反应的一部分,以确保细胞在暴露于应激刺激时存活。抗凋亡可能有助于致癌、肿瘤进展以及治疗抗性,因为目前大多数抗癌疗法,包括化疗以及放疗和免疫疗法,主要通过激活癌细胞中的细胞死亡途径(包括凋亡)来发挥作用。因此,更好地理解细胞应激刺激如何触发抗凋亡机制以及这如何导致肿瘤对凋亡性细胞死亡产生抗性的分子机制,有望为克服癌症中抗凋亡机制的合理方法提供基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/349f/2825553/8213fe06570f/IJCB2010-370835.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/349f/2825553/8213fe06570f/IJCB2010-370835.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/349f/2825553/8213fe06570f/IJCB2010-370835.001.jpg

相似文献

1
Evasion of apoptosis as a cellular stress response in cancer.凋亡逃避作为癌症中的一种细胞应激反应
Int J Cell Biol. 2010;2010:370835. doi: 10.1155/2010/370835. Epub 2010 Feb 18.
2
Tumor resistance to apoptosis.肿瘤对细胞凋亡的抗性。
Int J Cancer. 2009 Feb 1;124(3):511-5. doi: 10.1002/ijc.24064.
3
Apoptosis pathways and neuroblastoma therapy.凋亡途径与神经母细胞瘤治疗
Curr Pharm Des. 2009;15(4):430-5. doi: 10.2174/138161209787315846.
4
Targeting apoptosis signaling pathways for anticancer therapy.靶向细胞凋亡信号通路的抗肿瘤治疗。
Front Oncol. 2011 Aug 27;1:23. doi: 10.3389/fonc.2011.00023. eCollection 2011.
5
Apoptosis: A Target for Anticancer Therapy.细胞凋亡:抗癌治疗的新靶点。
Int J Mol Sci. 2018 Feb 2;19(2):448. doi: 10.3390/ijms19020448.
6
Targeting apoptosis pathways in cancer therapy.癌症治疗中针对凋亡途径
Curr Cancer Drug Targets. 2004 Nov;4(7):569-76. doi: 10.2174/1568009043332763.
7
Death receptor signaling in cancer therapy.癌症治疗中的死亡受体信号传导
Curr Med Chem Anticancer Agents. 2003 Jul;3(4):253-62. doi: 10.2174/1568011033482404.
8
Targeting apoptosis resistance in rhabdomyosarcoma.靶向横纹肌肉瘤中的凋亡抗性。
Curr Cancer Drug Targets. 2008 Sep;8(6):536-44. doi: 10.2174/156800908785699333.
9
Misfolded proteins bind and activate death receptor 5 to trigger apoptosis during unresolved endoplasmic reticulum stress.错误折叠的蛋白质与死亡受体 5 结合并激活,以在未解决的内质网应激期间引发细胞凋亡。
Elife. 2020 Jan 6;9:e52291. doi: 10.7554/eLife.52291.
10
Apoptosis pathways in neuroblastoma therapy.神经母细胞瘤治疗中的凋亡途径。
Cancer Lett. 2003 Jul 18;197(1-2):131-5. doi: 10.1016/s0304-3835(03)00091-0.

引用本文的文献

1
Exploring natural products as apoptosis modulators in cancers: insights into natural product-based therapeutic strategies.探索天然产物作为癌症中的细胞凋亡调节剂:对基于天然产物的治疗策略的见解。
Naunyn Schmiedebergs Arch Pharmacol. 2025 Feb 27. doi: 10.1007/s00210-025-03876-8.
2
Enhancement of the Sensitivity of the Acute Lymphoblastic Leukemia Cells to ABT-737 by Formononetin.芒柄花素增强急性淋巴细胞白血病细胞对ABT-737的敏感性
Int J Mol Cell Med. 2024;13(3):259-271. doi: 10.22088/IJMCM.BUMS.13.3.259.
3
Novel Thienopyrimidine-Hydrazinyl Compounds Induce DRP1-Mediated Non-Apoptotic Cell Death in Triple-Negative Breast Cancer Cells.

本文引用的文献

1
BCL-2: pro-or anti-oxidant?BCL-2:促氧化剂还是抗氧化剂?
Front Biosci (Elite Ed). 2009 Jun 1;1(1):263-8. doi: 10.2741/E25.
2
Tumor resistance to apoptosis.肿瘤对细胞凋亡的抗性。
Int J Cancer. 2009 Feb 1;124(3):511-5. doi: 10.1002/ijc.24064.
3
IAP-targeted therapies for cancer.针对癌症的IAP靶向疗法。
新型噻吩并嘧啶-肼基化合物诱导三阴性乳腺癌细胞中由动力相关蛋白1介导的非凋亡性细胞死亡。
Cancers (Basel). 2024 Jul 23;16(15):2621. doi: 10.3390/cancers16152621.
4
Harnessing the potential of hydrogels for advanced therapeutic applications: current achievements and future directions.水凝胶在先进治疗应用中的潜力:当前的成就和未来的方向。
Signal Transduct Target Ther. 2024 Jul 1;9(1):166. doi: 10.1038/s41392-024-01852-x.
5
Necroptosis induced by ruthenium (II) complexes as mitochondrial disruptors.钌(II)配合物作为线粒体破坏剂诱导的坏死性凋亡。
Cell Death Discov. 2024 May 28;10(1):261. doi: 10.1038/s41420-024-02033-z.
6
Induction of heat shock protein expression in SP2/0 transgenic cells and its effect on the production of monoclonal antibodies.诱导 SP2/0 转基因细胞表达热休克蛋白及其对单克隆抗体生产的影响。
PLoS One. 2024 May 2;19(5):e0300702. doi: 10.1371/journal.pone.0300702. eCollection 2024.
7
Salivary Gland Bioengineering.唾液腺生物工程
Bioengineering (Basel). 2023 Dec 26;11(1):28. doi: 10.3390/bioengineering11010028.
8
Dual Implications of Nanosilver-Induced Autophagy: Nanotoxicity and Anti-Cancer Effects.纳米银诱导自噬的双重意义:纳米毒性和抗癌作用。
Int J Mol Sci. 2023 Oct 20;24(20):15386. doi: 10.3390/ijms242015386.
9
Transferrin-Targeted Liposomes in Glioblastoma Therapy: A Review.转铁蛋白靶向脂质体在脑胶质瘤治疗中的研究进展
Int J Mol Sci. 2023 Aug 26;24(17):13262. doi: 10.3390/ijms241713262.
10
Review on Metal-Based Theranostic Nanoparticles for Cancer Therapy and Imaging.金属基诊疗一体化纳米粒子用于癌症治疗和成像的研究进展
Technol Cancer Res Treat. 2023 Jan-Dec;22:15330338231191493. doi: 10.1177/15330338231191493.
Oncogene. 2008 Oct 20;27(48):6252-75. doi: 10.1038/onc.2008.302.
4
Targeting inhibitor of apoptosis proteins (IAPs) for cancer therapy.靶向凋亡抑制蛋白(IAPs)用于癌症治疗。
Anticancer Agents Med Chem. 2008 Jun;8(5):533-9. doi: 10.2174/187152008784533107.
5
The p38 MAPK stress pathway as a tumor suppressor or more?p38丝裂原活化蛋白激酶应激通路仅仅是一种肿瘤抑制因子,还是有更多作用?
Front Biosci. 2008 May 1;13:3581-93. doi: 10.2741/2951.
6
Targeting the extrinsic apoptosis pathway in cancer.靶向癌症中的外源性凋亡途径。
Cytokine Growth Factor Rev. 2008 Jun-Aug;19(3-4):325-31. doi: 10.1016/j.cytogfr.2008.04.001. Epub 2008 May 20.
7
Cell death in health and disease.健康与疾病中的细胞死亡。
J Cell Mol Med. 2007 Nov-Dec;11(6):1214-24. doi: 10.1111/j.1582-4934.2007.00150.x. Epub 2007 Nov 20.
8
Rationales for expression and altered expression of apoptotic protease activating factor-1 gene in gastric cancer.凋亡蛋白酶激活因子-1基因在胃癌中的表达及表达改变的理论依据。
World J Gastroenterol. 2007 Oct 14;13(38):5060-4. doi: 10.3748/wjg.v13.i38.5060.
9
Mitochondrial regulation of caspase activation by cytochrome oxidase and tetramethylphenylenediamine via cytosolic cytochrome c redox state.细胞色素氧化酶和四甲基对苯二胺通过胞质细胞色素c氧化还原状态对胱天蛋白酶激活的线粒体调节。
J Biol Chem. 2007 Oct 26;282(43):31124-30. doi: 10.1074/jbc.M700322200. Epub 2007 Aug 9.
10
FLIP inhibits endothelial cell apoptosis during hyperoxia by suppressing Bax.FLIP通过抑制Bax来抑制高氧状态下的内皮细胞凋亡。
Free Radic Biol Med. 2007 May 15;42(10):1599-609. doi: 10.1016/j.freeradbiomed.2007.02.020. Epub 2007 Feb 28.