• 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

靶向抗凋亡Bcl-2家族成员用于癌症治疗。

Targeting the anti-apoptotic Bcl-2 family members for the treatment of cancer.

作者信息

Weyhenmeyer B, Murphy A C, Prehn J H M, Murphy B M

机构信息

Centre for Systems Medicine, Department of Physiology and Medical Physics, St. Stephen's Green, Dublin 2, Ireland.

出版信息

Exp Oncol. 2012 Oct;34(3):192-9.

PMID:23070004
Abstract

Most cells express a variety of both anti-apoptotic and pro-apoptotic Bcl-2 proteins and the interaction within this family dictates whether a cell survives or dies. The dysregulation of the anti-anti-apoptotic Bcl-2 family members is one of the defining features of cancer cells in comparison to normal cells, and significantly contributes to the resistance of cancer cells to current treatment modalities. This anti-apoptotic subfamily of proteins is now a major target in the development of new methods to improve treatment outcomes for cancer patients. Several drugs directed at inhibiting Bcl-2 and related anti-apoptotic proteins have been developed with some showing considerable promise in the clinic. This Review presents the current knowledge of the role of the anti-apoptotic Bcl-2 family in cancer cells, as well as current and future perspectives on targeting this subfamily of proteins for therapeutic intervention in human malignancies. This article is part of a Special Issue entitled "Apoptosis: Four Decades Later".

摘要

大多数细胞都表达多种抗凋亡和促凋亡的Bcl-2蛋白,该蛋白家族内的相互作用决定了细胞的生死存亡。与正常细胞相比,抗凋亡Bcl-2家族成员的失调是癌细胞的一个决定性特征,并显著导致癌细胞对当前治疗方式产生抗性。现在,这个抗凋亡蛋白亚家族已成为开发改善癌症患者治疗效果新方法的主要靶点。已经研发出几种针对抑制Bcl-2及相关抗凋亡蛋白的药物,其中一些在临床上显示出了相当大的前景。本综述介绍了抗凋亡Bcl-2家族在癌细胞中的作用的当前知识,以及针对该蛋白亚家族进行人类恶性肿瘤治疗干预的当前和未来观点。本文是名为“细胞凋亡:四十年后”的特刊的一部分。

相似文献

1
Targeting the anti-apoptotic Bcl-2 family members for the treatment of cancer.靶向抗凋亡Bcl-2家族成员用于癌症治疗。
Exp Oncol. 2012 Oct;34(3):192-9.
2
Small inhibitor of Bcl-2, HA14-1, selectively enhanced the apoptotic effect of cisplatin by modulating Bcl-2 family members in MDA-MB-231 breast cancer cells.Bcl-2小分子抑制剂HA14-1通过调节MDA-MB-231乳腺癌细胞中的Bcl-2家族成员,选择性增强顺铂的凋亡作用。
Breast Cancer Res Treat. 2010 Jan;119(2):271-81. doi: 10.1007/s10549-009-0343-z. Epub 2009 Feb 24.
3
Role of Bcl-2 in tumour cell survival and implications for pharmacotherapy.Bcl-2 在肿瘤细胞存活中的作用及其对药物治疗的意义。
J Pharm Pharmacol. 2012 Dec;64(12):1695-702. doi: 10.1111/j.2042-7158.2012.01526.x. Epub 2012 Apr 25.
4
Inhibition of Bcl-2 and Bcl-X enhances chemotherapy sensitivity in hepatoblastoma cells.抑制 Bcl-2 和 Bcl-X 可增强肝癌细胞对化疗的敏感性。
Pediatr Blood Cancer. 2010 Dec 1;55(6):1089-95. doi: 10.1002/pbc.22740.
5
BCL-2 family isoforms in apoptosis and cancer.BCL-2 家族在细胞凋亡和癌症中的亚型。
Cell Death Dis. 2019 Feb 21;10(3):177. doi: 10.1038/s41419-019-1407-6.
6
MicroRNA regulation of core apoptosis pathways in cancer.微小 RNA 对癌症核心凋亡途径的调控。
Eur J Cancer. 2011 Jan;47(2):163-74. doi: 10.1016/j.ejca.2010.11.005. Epub 2010 Dec 8.
7
Differential effects of anti-apoptotic Bcl-2 family members Mcl-1, Bcl-2, and Bcl-xL on celecoxib-induced apoptosis.抗凋亡Bcl-2家族成员Mcl-1、Bcl-2和Bcl-xL对塞来昔布诱导凋亡的不同作用。
Biochem Pharmacol. 2010 Jan 1;79(1):10-20. doi: 10.1016/j.bcp.2009.07.021. Epub 2009 Aug 7.
8
Bcl-2 family proteins as targets for anticancer drug design.作为抗癌药物设计靶点的Bcl-2家族蛋白
Oncogene. 2000 Dec 27;19(56):6627-31. doi: 10.1038/sj.onc.1204087.
9
Induction of apoptosis in prostate carcinoma cells by BH3 peptides which inhibit Bak/Bcl-2 interactions.通过抑制Bak/Bcl-2相互作用的BH3肽诱导前列腺癌细胞凋亡。
Br J Cancer. 2001 Jul 6;85(1):115-21. doi: 10.1054/bjoc.2001.1850.
10
Pro- and anti-apoptotic members of the Bcl-2 family in skeletal muscle: a distinct role for Bcl-2 in later stages of myogenesis.骨骼肌中Bcl-2家族的促凋亡和抗凋亡成员:Bcl-2在肌生成后期的独特作用。
Dev Dyn. 2001 Jan;220(1):18-26. doi: 10.1002/1097-0177(2000)9999:9999<::AID-DVDY1088>3.0.CO;2-#.

引用本文的文献

1
Comparative Analysis of Chemotherapy Resistance Mechanisms in Humans and Companion Animals.人类与伴侣动物化疗耐药机制的比较分析
Vet Sci. 2025 Aug 12;12(8):747. doi: 10.3390/vetsci12080747.
2
Molecular complexity of diffuse large B-cell lymphoma: a molecular perspective and therapeutic implications.弥漫性大 B 细胞淋巴瘤的分子复杂性:分子视角与治疗意义。
J Appl Genet. 2024 Feb;65(1):57-72. doi: 10.1007/s13353-023-00804-5. Epub 2023 Nov 25.
3
Overcoming apoptotic resistance afforded by Bcl-2 in lymphoid tumor cells: a critical role for dexamethasone.
克服Bcl-2在淋巴瘤细胞中赋予的凋亡抗性:地塞米松的关键作用。
Cell Death Discov. 2022 Dec 20;8(1):494. doi: 10.1038/s41420-022-01285-x.
4
Toosendanin induces apoptosis of MKN‑45 human gastric cancer cells partly through miR‑23a‑3p‑mediated downregulation of BCL2.川陈皮素通过 miR-23a-3p 介导的 BCL2 下调部分诱导 MKN-45 人胃癌细胞凋亡。
Mol Med Rep. 2020 Sep;22(3):1793-1802. doi: 10.3892/mmr.2020.11263. Epub 2020 Jun 22.
5
MicroRNAs signatures, bioinformatics analysis of miRNAs, miRNA mimics and antagonists, and miRNA therapeutics in osteosarcoma.骨肉瘤中的微小RNA特征、微小RNA的生物信息学分析、微小RNA模拟物和拮抗剂以及微小RNA治疗
Cancer Cell Int. 2020 Jun 17;20:254. doi: 10.1186/s12935-020-01342-4. eCollection 2020.
6
Implementing Patient-Derived Xenografts to Assess the Effectiveness of Cyclin-Dependent Kinase Inhibitors in Glioblastoma.应用患者来源的异种移植模型评估细胞周期蛋白依赖性激酶抑制剂治疗胶质母细胞瘤的有效性
Cancers (Basel). 2019 Dec 12;11(12):2005. doi: 10.3390/cancers11122005.
7
Mytoxin B and Myrothecine A Induce Apoptosis in Human Hepatocarcinoma Cell Line SMMC-7721 via PI3K/Akt Signaling Pathway.蜂毒素 B 和米托蒽醌 A 通过 PI3K/Akt 信号通路诱导人肝癌细胞系 SMMC-7721 凋亡。
Molecules. 2019 Jun 20;24(12):2291. doi: 10.3390/molecules24122291.
8
The TRAIL: TRAILshort Axis in HIV Immunopathology.肿瘤坏死因子相关凋亡诱导配体:HIV免疫病理学中的TRAIL短轴
Crit Rev Immunol. 2018;38(6):491-503. doi: 10.1615/CritRevImmunol.2019029632.
9
Therapeutic Potency of Nanoformulations of siRNAs and shRNAs in Animal Models of Cancers.小干扰RNA(siRNA)和短发夹RNA(shRNA)纳米制剂在癌症动物模型中的治疗效力
Pharmaceutics. 2018 May 26;10(2):65. doi: 10.3390/pharmaceutics10020065.
10
Paclitaxel Reduces Axonal Bclw to Initiate IPR1-Dependent Axon Degeneration.紫杉醇降低轴突Bclw以启动IPR1依赖性轴突退化。
Neuron. 2017 Oct 11;96(2):373-386.e6. doi: 10.1016/j.neuron.2017.09.034.