• 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

Drug therapy: Exploiting synthetic lethality to improve cancer therapy.

作者信息

Brunen Diede, Bernards René

机构信息

Division of Molecular Carcinogenesis, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, Netherlands.

出版信息

Nat Rev Clin Oncol. 2017 Jun;14(6):331-332. doi: 10.1038/nrclinonc.2017.46. Epub 2017 Mar 29.

DOI:10.1038/nrclinonc.2017.46
PMID:28352131
Abstract
摘要

相似文献

1
Drug therapy: Exploiting synthetic lethality to improve cancer therapy.药物治疗:利用合成致死性改善癌症治疗。
Nat Rev Clin Oncol. 2017 Jun;14(6):331-332. doi: 10.1038/nrclinonc.2017.46. Epub 2017 Mar 29.
2
Prostate cancer: Fatal interaction: a new target identified.前列腺癌:致命相互作用:一个新靶点被发现。
Nat Rev Urol. 2017 May;14(5):258-259. doi: 10.1038/nrurol.2017.29. Epub 2017 Feb 21.
3
Targeting p300 Addiction in CBP-Deficient Cancers Causes Synthetic Lethality by Apoptotic Cell Death due to Abrogation of MYC Expression.靶向 CBP 缺陷型癌症中的 p300 成瘾会导致细胞凋亡性细胞死亡,从而引起 MYC 表达缺失的合成致死性。
Cancer Discov. 2016 Apr;6(4):430-45. doi: 10.1158/2159-8290.CD-15-0754. Epub 2015 Nov 24.
4
Functional genomics identifies specific vulnerabilities in PTEN-deficient breast cancer.功能基因组学鉴定出 PTEN 缺陷型乳腺癌的特定脆弱性。
Breast Cancer Res. 2018 Mar 22;20(1):22. doi: 10.1186/s13058-018-0949-3.
5
The Chromodomain Helicase DNA-Binding Chromatin Remodelers: Family Traits that Protect from and Promote Cancer.染色质结构域解旋酶DNA结合染色质重塑因子:预防和促进癌症的家族特征
Cold Spring Harb Perspect Med. 2017 Apr 3;7(4):a026450. doi: 10.1101/cshperspect.a026450.
6
Synthetic lethality prediction in DNA damage repair, chromatin remodeling and the cell cycle using multi-omics data from cell lines and patients.使用来自细胞系和患者的多组学数据预测 DNA 损伤修复、染色质重塑和细胞周期中的合成致死性。
Sci Rep. 2023 Apr 29;13(1):7049. doi: 10.1038/s41598-023-34161-4.
7
Inactivating mutations in SWI/SNF chromatin remodeling genes in human cancer.人类癌症中 SWI/SNF 染色质重塑基因的失活突变。
Jpn J Clin Oncol. 2013 Sep;43(9):849-55. doi: 10.1093/jjco/hyt101. Epub 2013 Jul 30.
8
The SMARCA2/4 ATPase Domain Surpasses the Bromodomain as a Drug Target in SWI/SNF-Mutant Cancers: Insights from cDNA Rescue and PFI-3 Inhibitor Studies.在SWI/SNF突变型癌症中,SMARCA2/4 ATP酶结构域作为药物靶点优于溴结构域:来自cDNA拯救和PFI-3抑制剂研究的见解。
Cancer Res. 2015 Sep 15;75(18):3865-3878. doi: 10.1158/0008-5472.CAN-14-3798. Epub 2015 Jul 2.
9
Systematic identification of synthetic lethal mutations with reduced-genome Escherichia coli: synthetic genetic interactions among yoaA, xthA and holC related to survival from MMS exposure.对基因组减少的大肠杆菌中合成致死突变的系统鉴定:yoaA、xthA和holC之间与甲基磺酸甲酯暴露存活相关的合成遗传相互作用。
Genes Genet Syst. 2016 Nov 26;91(3):183-188. doi: 10.1266/ggs.15-00068. Epub 2016 May 2.
10
An in-silico approach to predict and exploit synthetic lethality in cancer metabolism.一种通过计算机模拟方法预测和利用癌症代谢中的合成致死性。
Nat Commun. 2017 Sep 6;8(1):459. doi: 10.1038/s41467-017-00555-y.

引用本文的文献

1
Synthetic lethal approaches to target cancers with loss of PTEN function.针对PTEN功能缺失的癌症的合成致死方法。
Genes Dis. 2023 Nov;10(6):2511-2527. doi: 10.1016/j.gendis.2022.12.015.
2
Virally programmed extracellular vesicles sensitize cancer cells to oncolytic virus and small molecule therapy.病毒编程的细胞外囊泡使癌细胞对溶瘤病毒和小分子治疗敏感。
Nat Commun. 2022 Apr 7;13(1):1898. doi: 10.1038/s41467-022-29526-8.
3
Valproic Acid Regulates HR and Cell Cycle Through MUS81-pRPA2 Pathway in Response to Hydroxyurea.丙戊酸通过MUS81-pRPA2途径调节心率和细胞周期以应对羟基脲。

本文引用的文献

1
Long-Term Outcomes of Imatinib Treatment for Chronic Myeloid Leukemia.伊马替尼治疗慢性髓性白血病的长期疗效
N Engl J Med. 2017 Mar 9;376(10):917-927. doi: 10.1056/NEJMoa1609324.
2
Synthetic essentiality of chromatin remodelling factor CHD1 in PTEN-deficient cancer.染色质重塑因子CHD1在PTEN缺陷型癌症中的合成必需性
Nature. 2017 Feb 23;542(7642):484-488. doi: 10.1038/nature21357. Epub 2017 Feb 6.
3
Gene Essentiality Profiling Reveals Gene Networks and Synthetic Lethal Interactions with Oncogenic Ras.基因必需性分析揭示基因网络以及与致癌性Ras的合成致死相互作用。
Front Oncol. 2021 Aug 27;11:681278. doi: 10.3389/fonc.2021.681278. eCollection 2021.
4
Modeling Heterogeneity of Triple-Negative Breast Cancer Uncovers a Novel Combinatorial Treatment Overcoming Primary Drug Resistance.三阴性乳腺癌异质性建模揭示一种克服原发性耐药的新型联合治疗方法。
Adv Sci (Weinh). 2020 Dec 16;8(3):2003049. doi: 10.1002/advs.202003049. eCollection 2021 Feb.
5
Pathway-Based Drug-Repurposing Schemes in Cancer: The Role of Translational Bioinformatics.癌症中基于通路的药物再利用策略:转化生物信息学的作用
Front Oncol. 2021 Jan 14;10:605680. doi: 10.3389/fonc.2020.605680. eCollection 2020.
6
A Novel Platform to Test In Vivo Single Gene Dependencies in t(8,21) and t(15,17) AML Confirms Zeb2 as Leukemia Target.一种用于检测t(8,21)和t(15,17)急性髓系白血病体内单基因依赖性的新型平台证实Zeb2为白血病靶点。
Cancers (Basel). 2020 Dec 14;12(12):3768. doi: 10.3390/cancers12123768.
7
Combined inhibition of Ref-1 and STAT3 leads to synergistic tumour inhibition in multiple cancers using 3D and in vivo tumour co-culture models.联合抑制 Ref-1 和 STAT3 使用 3D 肿瘤共培养模型和体内肿瘤共培养模型可协同抑制多种癌症。
J Cell Mol Med. 2021 Jan;25(2):784-800. doi: 10.1111/jcmm.16132. Epub 2020 Dec 3.
8
WDHD1 is essential for the survival of PTEN-inactive triple-negative breast cancer.WDHD1 对于 PTEN 失活的三阴性乳腺癌的存活是必需的。
Cell Death Dis. 2020 Nov 21;11(11):1001. doi: 10.1038/s41419-020-03210-5.
9
Synthetic lethal combination targeting BET uncovered intrinsic susceptibility of TNBC to ferroptosis.靶向BET的合成致死组合揭示了三阴性乳腺癌对铁死亡的内在易感性。
Sci Adv. 2020 Aug 21;6(34). doi: 10.1126/sciadv.aba8968. Print 2020 Aug.
10
Importance of genetic screens in precision oncology.基因筛查在精准肿瘤学中的重要性。
ESMO Open. 2019 May 24;4(3):e000505. doi: 10.1136/esmoopen-2019-000505. eCollection 2019.
Cell. 2017 Feb 23;168(5):890-903.e15. doi: 10.1016/j.cell.2017.01.013. Epub 2017 Feb 2.
4
Opportunities and challenges provided by crosstalk between signalling pathways in cancer.癌症中信号通路间相互作用所带来的机遇与挑战
Oncogene. 2016 Mar 3;35(9):1073-9. doi: 10.1038/onc.2015.151. Epub 2015 May 18.
5
Unresponsiveness of colon cancer to BRAF(V600E) inhibition through feedback activation of EGFR.结直肠癌对 BRAF(V600E)抑制的无应答性通过 EGFR 的反馈激活。
Nature. 2012 Jan 26;483(7387):100-3. doi: 10.1038/nature10868.
6
Non-oncogene addiction and the stress phenotype of cancer cells.非癌基因成瘾与癌细胞的应激表型
Cell. 2007 Sep 21;130(6):986-8. doi: 10.1016/j.cell.2007.09.007.
7
Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy.将BRCA突变细胞中的DNA修复缺陷作为一种治疗策略。
Nature. 2005 Apr 14;434(7035):917-21. doi: 10.1038/nature03445.
8
Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase.用聚(ADP - 核糖)聚合酶抑制剂特异性杀伤BRCA2缺陷型肿瘤
Nature. 2005 Apr 14;434(7035):913-7. doi: 10.1038/nature03443.
9
Cancer. Addiction to oncogenes--the Achilles heal of cancer.癌症。对癌基因的依赖——癌症的阿喀琉斯之踵。
Science. 2002 Jul 5;297(5578):63-4. doi: 10.1126/science.1073096.