• 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

热休克蛋白90抑制剂:肿瘤治疗中的临床开发及未来机遇

Hsp90 inhibitors: clinical development and future opportunities in oncology therapy.

作者信息

Gao Zhenhai, Garcia-Echeverria Carlos, Jensen Michael Rugaard

机构信息

Novartis Pharma AG, Novartis Institutes for BioMedical Research, Basel, Switzerland.

出版信息

Curr Opin Drug Discov Devel. 2010 Mar;13(2):193-202.

PMID:20205053
Abstract

The development of small molecular mass Hsp90 inhibitors has become an increasingly competitive field of research in recent years. Progress in preclinical and clinical research has provided increasing evidence that Hsp90 represents a promising molecular target for the treatment of cancer and other diseases. Although many challenges remain, recent clinical trial results for the most clinically advanced inhibitors indicate that clinical proof of concept in oncology therapy is achievable, and that Hsp90 inhibitors have the potential to contribute to the collection of anticancer treatments available to clinicians and patients in the near future.

摘要

近年来,小分子质量热休克蛋白90(Hsp90)抑制剂的研发已成为竞争日益激烈的研究领域。临床前和临床研究的进展提供了越来越多的证据,表明Hsp90是治疗癌症和其他疾病的一个有前景的分子靶点。尽管仍存在许多挑战,但针对临床上最先进抑制剂的近期临床试验结果表明,肿瘤治疗的临床概念验证是可以实现的,并且Hsp90抑制剂有可能在不久的将来为临床医生和患者提供更多的抗癌治疗手段。

相似文献

1
Hsp90 inhibitors: clinical development and future opportunities in oncology therapy.热休克蛋白90抑制剂:肿瘤治疗中的临床开发及未来机遇
Curr Opin Drug Discov Devel. 2010 Mar;13(2):193-202.
2
Heat-shock protein 90 (Hsp90) as a molecular target for therapy of gastrointestinal cancer.热休克蛋白90(Hsp90)作为胃肠道癌治疗的分子靶点。
Anticancer Res. 2009 Jun;29(6):2031-42.
3
Hsp90 inhibitors: small molecules that transform the Hsp90 protein folding machinery into a catalyst for protein degradation.热休克蛋白90(Hsp90)抑制剂:将Hsp90蛋白质折叠机制转变为蛋白质降解催化剂的小分子。
Med Res Rev. 2006 May;26(3):310-38. doi: 10.1002/med.20052.
4
Heat shock protein 90: inhibitors in clinical trials.热休克蛋白90:临床试验中的抑制剂
J Med Chem. 2010 Jan 14;53(1):3-17. doi: 10.1021/jm9004708.
5
Targeting of multiple signalling pathways by heat shock protein 90 molecular chaperone inhibitors.热休克蛋白90分子伴侣抑制剂对多种信号通路的靶向作用
Endocr Relat Cancer. 2006 Dec;13 Suppl 1:S125-35. doi: 10.1677/erc.1.01324.
6
Inside the Hsp90 inhibitors binding mode through induced fit docking.通过诱导契合对接研究Hsp90抑制剂的结合模式。
J Mol Graph Model. 2009 Feb;27(6):712-22. doi: 10.1016/j.jmgm.2008.11.004. Epub 2008 Nov 8.
7
Combinatorial attack on multistep oncogenesis by inhibiting the Hsp90 molecular chaperone.通过抑制热休克蛋白90(Hsp90)分子伴侣对多步骤肿瘤发生进行组合攻击。
Cancer Lett. 2004 Apr 8;206(2):149-57. doi: 10.1016/j.canlet.2003.08.032.
8
[Heat shock protein 90: novel target for cancer therapy].[热休克蛋白90:癌症治疗的新靶点]
Ai Zheng. 2004 Aug;23(8):968-74.
9
Discovery and development of Hsp90 inhibitors: a promising pathway for cancer therapy.热休克蛋白 90 抑制剂的发现和研制:癌症治疗的一个有前景的途径。
Curr Opin Chem Biol. 2010 Jun;14(3):412-20. doi: 10.1016/j.cbpa.2010.03.019. Epub 2010 Apr 19.
10
Drugging the cancer chaperone HSP90: combinatorial therapeutic exploitation of oncogene addiction and tumor stress.靶向癌症伴侣蛋白HSP90:癌基因成瘾与肿瘤应激的联合治疗应用
Ann N Y Acad Sci. 2007 Oct;1113:202-16. doi: 10.1196/annals.1391.012. Epub 2007 May 18.

引用本文的文献

1
Hsp90 Inhibitor STA9090 Sensitizes Hepatocellular Carcinoma to Hyperthermia-Induced DNA Damage by Suppressing DNA-PKcs Protein Stability and mRNA Transcription.热休克蛋白 90 抑制剂 STA9090 通过抑制 DNA-PKcs 蛋白稳定性和 mRNA 转录来增强肝癌对热疗诱导的 DNA 损伤的敏感性。
Mol Cancer Ther. 2021 Oct;20(10):1880-1892. doi: 10.1158/1535-7163.MCT-21-0215. Epub 2021 Aug 10.
2
Bioluminescence Imaging to Monitor the Effects of the Hsp90 Inhibitor NVP-AUY922 on NF-κB Pathway in Endometrial Cancer.生物发光成像监测热休克蛋白90抑制剂NVP - AUY922对子宫内膜癌中核因子κB通路的影响
Mol Imaging Biol. 2016 Aug;18(4):545-56. doi: 10.1007/s11307-015-0907-8.
3
Phase I dose-escalation study of the HSP90 inhibitor AUY922 in Japanese patients with advanced solid tumors.
AUY922(一种 HSP90 抑制剂)在日本晚期实体瘤患者中的 I 期剂量递增研究。
Cancer Chemother Pharmacol. 2014 Sep;74(3):629-36. doi: 10.1007/s00280-014-2521-x. Epub 2014 Jul 25.
4
Effect of novobiocin on the viability of human gingival fibroblasts (HGF-1).新生霉素对人牙龈成纤维细胞(HGF-1)活力的影响。
BMC Pharmacol Toxicol. 2014 May 1;15:25. doi: 10.1186/2050-6511-15-25.
5
Radiosensitizers in pancreatic cancer--preclinical and clinical exploits with molecularly targeted agents.胰腺癌的放射增敏剂——分子靶向药物的临床前和临床应用
Curr Probl Cancer. 2013 Sep-Oct;37(5):301-12. doi: 10.1016/j.currproblcancer.2013.10.008. Epub 2013 Oct 5.
6
Probing molecular mechanisms of the Hsp90 chaperone: biophysical modeling identifies key regulators of functional dynamics.探究 HSP90 伴侣蛋白的分子机制:生物物理建模确定功能动力学的关键调节剂。
PLoS One. 2012;7(5):e37605. doi: 10.1371/journal.pone.0037605. Epub 2012 May 18.
7
Advances in the discovery and development of heat-shock protein 90 inhibitors for cancer treatment.用于癌症治疗的热休克蛋白90抑制剂的发现与开发进展。
Expert Opin Drug Discov. 2011 May;6(5):559-587. doi: 10.1517/17460441.2011.563296.
8
Β-elemene inhibits Hsp90/Raf-1 molecular complex inducing apoptosis of glioblastoma cells.β-榄香烯抑制 Hsp90/Raf-1 分子复合物诱导脑胶质瘤细胞凋亡。
J Neurooncol. 2012 Apr;107(2):307-14. doi: 10.1007/s11060-011-0770-7. Epub 2011 Dec 11.
9
Hsp90β inhibition modulates nitric oxide production and nitric oxide-induced apoptosis in human chondrocytes.Hsp90β 抑制调节人软骨细胞中一氧化氮的产生和一氧化氮诱导的细胞凋亡。
BMC Musculoskelet Disord. 2011 Oct 17;12:237. doi: 10.1186/1471-2474-12-237.
10
Genomewide analysis of inherited variation associated with phosphorylation of PI3K/AKT/mTOR signaling proteins.全基因组分析与 PI3K/AKT/mTOR 信号蛋白磷酸化相关的遗传变异。
PLoS One. 2011;6(9):e24873. doi: 10.1371/journal.pone.0024873. Epub 2011 Sep 19.