• 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

蛋白酶体抑制剂与铂类疗法在实体瘤中协同作用的分子机制

Molecular mechanisms for synergistic effect of proteasome inhibitors with platinum-based therapy in solid tumors.

作者信息

Chao Angel, Wang Tzu-Hao

机构信息

Department of Obstetrics and Gynecology, Linkou Medical Center, Taoyuan, Taiwan.

Department of Obstetrics and Gynecology, Linkou Medical Center, Taoyuan, Taiwan; Genomic Medicine Research Core Laboratory, Linkou Medical Center, Chang Gung Memorial Hospital and Chang Gung University, Taoyuan, Taiwan; School of Traditional Chinese Medicine, College of Medicine, Chang Gung University, Taoyuan, Taiwan.

出版信息

Taiwan J Obstet Gynecol. 2016 Feb;55(1):3-8. doi: 10.1016/j.tjog.2015.12.004.

DOI:10.1016/j.tjog.2015.12.004
PMID:26927239
Abstract

The successful development of the proteasome inhibitor bortezomib as an anticancer drug has improved survival in patients with multiple myeloma. With the emergence of the newly US Food and Drug Administration-approved proteasome inhibitor carfilzomib, ongoing trials are investigating this compound and other proteasome inhibitors either alone or in combination with other chemotherapy drugs. However, in solid tumors, the efficacy of proteasome inhibitors has not lived up to expectations. Results regarding the potential clinical efficacy of bortezomib combined with other agents in the treatment of solid tumors are eagerly awaited. Recent identification of the molecular mechanisms (involving apoptosis and autophagy) by which bortezomib and cisplatin can overcome chemotherapy resistance and sensitize tumor cells to anticancer therapy can provide insights into the development of novel therapeutic strategies for patients with solid malignancies.

摘要

蛋白酶体抑制剂硼替佐米作为一种抗癌药物的成功研发,已提高了多发性骨髓瘤患者的生存率。随着美国食品药品监督管理局新批准的蛋白酶体抑制剂卡非佐米的出现,正在进行的试验正在单独或与其他化疗药物联合研究该化合物及其他蛋白酶体抑制剂。然而,在实体瘤中,蛋白酶体抑制剂的疗效并未达到预期。人们急切期待硼替佐米与其他药物联合治疗实体瘤的潜在临床疗效的结果。最近对硼替佐米和顺铂能够克服化疗耐药性并使肿瘤细胞对抗癌治疗敏感的分子机制(涉及凋亡和自噬)的鉴定,可为实体恶性肿瘤患者新治疗策略的开发提供见解。

相似文献

1
Molecular mechanisms for synergistic effect of proteasome inhibitors with platinum-based therapy in solid tumors.蛋白酶体抑制剂与铂类疗法在实体瘤中协同作用的分子机制
Taiwan J Obstet Gynecol. 2016 Feb;55(1):3-8. doi: 10.1016/j.tjog.2015.12.004.
2
Increased resistance to proteasome inhibitors in multiple myeloma mediated by cIAP2--implications for a combinatorial treatment.cIAP2介导的多发性骨髓瘤对蛋白酶体抑制剂耐药性增加——联合治疗的意义
Oncotarget. 2015 Aug 21;6(24):20621-35. doi: 10.18632/oncotarget.4139.
3
The novel β2-selective proteasome inhibitor LU-102 synergizes with bortezomib and carfilzomib to overcome proteasome inhibitor resistance of myeloma cells.新型β2选择性蛋白酶体抑制剂LU-102与硼替佐米和卡非佐米协同作用,克服骨髓瘤细胞对蛋白酶体抑制剂的耐药性。
Haematologica. 2015 Oct;100(10):1350-60. doi: 10.3324/haematol.2014.109421. Epub 2015 Jun 11.
4
Targeting Notch1 and proteasome as an effective strategy to suppress T-cell lymphoproliferative neoplasms.靶向Notch1和蛋白酶体作为抑制T细胞淋巴增殖性肿瘤的有效策略。
Oncotarget. 2015 Jun 20;6(17):14953-69. doi: 10.18632/oncotarget.3621.
5
Synergistic interaction between the novel histone deacetylase inhibitor ST2782 and the proteasome inhibitor bortezomib in platinum-sensitive and resistant ovarian carcinoma cells.新型组蛋白去乙酰化酶抑制剂 ST2782 与蛋白酶体抑制剂硼替佐米在铂类敏感和耐药卵巢癌细胞中的协同作用。
J Inorg Biochem. 2012 Aug;113:94-101. doi: 10.1016/j.jinorgbio.2012.04.007. Epub 2012 Apr 27.
6
VR23: A Quinoline-Sulfonyl Hybrid Proteasome Inhibitor That Selectively Kills Cancer via Cyclin E-Mediated Centrosome Amplification.VR23:一种喹啉-磺酰基杂合蛋白酶体抑制剂,通过细胞周期蛋白 E 介导的中心体扩增选择性杀死癌细胞。
Cancer Res. 2015 Oct 1;75(19):4164-75. doi: 10.1158/0008-5472.CAN-14-3370. Epub 2015 Aug 3.
7
The Proteasome Inhibitor Bortezomib Maintains Osteocyte Viability in Multiple Myeloma Patients by Reducing Both Apoptosis and Autophagy: A New Function for Proteasome Inhibitors.蛋白酶体抑制剂硼替佐米通过减少凋亡和自噬维持多发性骨髓瘤患者骨细胞的活力:蛋白酶体抑制剂的新功能
J Bone Miner Res. 2016 Apr;31(4):815-27. doi: 10.1002/jbmr.2741. Epub 2015 Dec 14.
8
Syrbactin proteasome inhibitor TIR-199 overcomes bortezomib chemoresistance and inhibits multiple myeloma tumor growth in vivo.Syrbactin 蛋白酶体抑制剂 TIR-199 克服硼替佐米化疗耐药性并抑制体内多发性骨髓瘤肿瘤生长。
Leuk Res. 2020 Jan;88:106271. doi: 10.1016/j.leukres.2019.106271. Epub 2019 Nov 12.
9
P-Glycoprotein Inhibition Sensitizes Human Breast Cancer Cells to Proteasome Inhibitors.P-糖蛋白抑制使人类乳腺癌细胞对蛋白酶体抑制剂敏感。
J Cell Biochem. 2017 May;118(5):1239-1248. doi: 10.1002/jcb.25783. Epub 2017 Jan 10.
10
Nuclear Export of Ubiquitinated Proteins Determines the Sensitivity of Colorectal Cancer to Proteasome Inhibitor.泛素化蛋白的核输出决定了结直肠癌对蛋白酶体抑制剂的敏感性。
Mol Cancer Ther. 2017 Apr;16(4):717-728. doi: 10.1158/1535-7163.MCT-16-0553. Epub 2016 Nov 30.

引用本文的文献

1
Identification of multidrug chemoresistant genes in head and neck squamous cell carcinoma cells.鉴定头颈部鳞状细胞癌细胞中的多药耐药基因。
Mol Cancer. 2023 Sep 4;22(1):146. doi: 10.1186/s12943-023-01846-3.
2
Investigation of the therapeutic role of native plant compounds against colorectal cancer based on system biology and virtual screening.基于系统生物学和虚拟筛选的本土植物化合物治疗结直肠癌作用的研究。
Sci Rep. 2023 Jul 15;13(1):11451. doi: 10.1038/s41598-023-38134-5.
3
LINC00963/miR-4458 regulates the effect of oxaliplatin in gastric cancer by mediating autophagic flux through targeting of ATG16L1.
LINC00963/miR-4458 通过靶向 ATG16L1 调控自噬流从而影响胃癌对奥沙利铂的作用。
Sci Rep. 2021 Oct 25;11(1):20951. doi: 10.1038/s41598-021-98728-9.
4
Proteasome Complexes and Their Heterogeneity in Colorectal, Breast and Pancreatic Cancers.蛋白酶体复合物及其在结直肠癌、乳腺癌和胰腺癌中的异质性
J Cancer. 2021 Mar 5;12(9):2472-2487. doi: 10.7150/jca.52414. eCollection 2021.
5
Does the proteasome inhibitor bortezomib sensitize to DNA-damaging therapy in gastroenteropancreatic neuroendocrine neoplasms? - A preclinical assessment in vitro and in vivo.蛋白酶体抑制剂硼替佐米是否能使胃肠胰神经内分泌肿瘤对 DNA 损伤治疗敏感?——体外和体内的临床前评估。
Neoplasia. 2021 Jan;23(1):80-98. doi: 10.1016/j.neo.2020.11.004. Epub 2020 Nov 25.
6
Proteasome inhibition-a new target for brain tumours.蛋白酶体抑制——脑肿瘤的新靶点。
Cell Death Discov. 2019 Dec 4;5:147. doi: 10.1038/s41420-019-0227-x. eCollection 2019.
7
Novel Copper Complexes That Inhibit the Proteasome and Trigger Apoptosis in Triple-Negative Breast Cancer Cells.新型铜配合物可抑制蛋白酶体并引发三阴性乳腺癌细胞凋亡。
ACS Med Chem Lett. 2019 Jul 25;10(9):1328-1335. doi: 10.1021/acsmedchemlett.9b00284. eCollection 2019 Sep 12.
8
Targeting Proteotoxic Stress in Cancer: A Review of the Role that Protein Quality Control Pathways Play in Oncogenesis.靶向癌症中的蛋白毒性应激:蛋白质质量控制途径在肿瘤发生中作用的综述
Cancers (Basel). 2019 Jan 9;11(1):66. doi: 10.3390/cancers11010066.
9
Pirh2 mediates the sensitivity of myeloma cells to bortezomib via canonical NF-κB signaling pathway.PIrH2 通过经典 NF-κB 信号通路介导骨髓瘤细胞对硼替佐米的敏感性。
Protein Cell. 2018 Sep;9(9):770-784. doi: 10.1007/s13238-017-0500-9. Epub 2018 Feb 13.
10
Second-generation proteasome inhibitor carfilzomib enhances doxorubicin-induced cytotoxicity and apoptosis in breast cancer cells.第二代蛋白酶体抑制剂卡非佐米增强阿霉素诱导的乳腺癌细胞的细胞毒性和凋亡。
Oncotarget. 2016 Nov 8;7(45):73697-73710. doi: 10.18632/oncotarget.12048.