• 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

利用DNA修复缺陷开发新型癌症疗法。

Exploiting DNA repair defects for novel cancer therapies.

作者信息

van Gent Dik C, Kanaar Roland

机构信息

Department of Molecular Genetics, Cancer Genomics Netherlands, Erasmus University Medical Center, Rotterdam 3015, Netherlands.

Department of Molecular Genetics, Cancer Genomics Netherlands, Erasmus University Medical Center, Rotterdam 3015, Netherlands Department of Radiation Oncology, Erasmus University Medical Center, Rotterdam 3015, Netherlands

出版信息

Mol Biol Cell. 2016 Jul 15;27(14):2145-8. doi: 10.1091/mbc.E15-10-0698.

DOI:10.1091/mbc.E15-10-0698
PMID:27418635
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4945134/
Abstract

Most human tumors accumulate a multitude of genetic changes due to defects in the DNA damage response. Recently, small-molecule inhibitors have been developed that target cells with specific DNA repair defects, providing hope for precision treatment of such tumors. Here we discuss the rationale behind these therapies and how an important bottleneck-patient selection-can be approached.

摘要

由于DNA损伤反应缺陷,大多数人类肿瘤会积累大量基因变化。最近,已开发出针对具有特定DNA修复缺陷细胞的小分子抑制剂,为这类肿瘤的精准治疗带来了希望。在此,我们讨论这些疗法背后的基本原理以及如何解决一个重要的瓶颈问题——患者选择。

相似文献

1
Exploiting DNA repair defects for novel cancer therapies.利用DNA修复缺陷开发新型癌症疗法。
Mol Biol Cell. 2016 Jul 15;27(14):2145-8. doi: 10.1091/mbc.E15-10-0698.
2
DNA Double Strand Break Repair - Related Synthetic Lethality.DNA 双链断裂修复相关的合成致死性。
Curr Med Chem. 2019;26(8):1446-1482. doi: 10.2174/0929867325666180201114306.
3
DNA Repair.DNA修复
Recent Results Cancer Res. 2016;198:1-24. doi: 10.1007/978-3-662-49651-0_1.
4
Recent advances in cancer therapy targeting proteins involved in DNA double-strand break repair.近年来,针对参与 DNA 双链断裂修复的蛋白质的癌症治疗取得了进展。
Clin Cancer Res. 2009 Oct 15;15(20):6314-20. doi: 10.1158/1078-0432.CCR-09-0096. Epub 2009 Oct 6.
5
YU238259 Is a Novel Inhibitor of Homology-Dependent DNA Repair That Exhibits Synthetic Lethality and Radiosensitization in Repair-Deficient Tumors.YU238259是一种新型的同源依赖性DNA修复抑制剂,在修复缺陷型肿瘤中表现出合成致死性和放射增敏作用。
Mol Cancer Res. 2015 Oct;13(10):1389-97. doi: 10.1158/1541-7786.MCR-15-0036. Epub 2015 Jun 26.
6
Targeting the DNA damage response for cancer therapy.靶向DNA损伤反应进行癌症治疗。
DNA Repair (Amst). 2009 Sep 2;8(9):1153-65. doi: 10.1016/j.dnarep.2009.04.011. Epub 2009 Jun 5.
7
Molecular pathways: exploiting tumor-specific molecular defects in DNA repair pathways for precision cancer therapy.分子途径:利用肿瘤特异性 DNA 修复途径中的分子缺陷进行精准癌症治疗。
Clin Cancer Res. 2014 Dec 1;20(23):5882-7. doi: 10.1158/1078-0432.CCR-14-1165.
8
DNA repair targeting and radiotherapy: a focus on the therapeutic ratio.DNA 修复靶向与放疗:关注治疗比。
Semin Radiat Oncol. 2010 Oct;20(4):217-22. doi: 10.1016/j.semradonc.2010.06.003.
9
Targeting DNA repair mechanisms in cancer.针对癌症的 DNA 修复机制。
Pharmacol Ther. 2013 Mar;137(3):298-308. doi: 10.1016/j.pharmthera.2012.10.009. Epub 2012 Oct 27.
10
DNA repair: from genome maintenance to biomarker and therapeutic target.DNA 修复:从基因组维护到生物标志物和治疗靶点。
Clin Cancer Res. 2011 Nov 15;17(22):6973-84. doi: 10.1158/1078-0432.CCR-11-0761. Epub 2011 Sep 9.

引用本文的文献

1
Inhibition of non-homologous end joining mitigates paclitaxel resistance resulting from mitotic slippage in non-small cell lung cancer.抑制非同源末端连接可减轻非小细胞肺癌中因有丝分裂滑溜导致的紫杉醇耐药性。
Cell Cycle. 2023 Sep;22(17):1854-1864. doi: 10.1080/15384101.2023.2243761. Epub 2023 Aug 17.
2
MAGI1 Prevents Senescence and Promotes the DNA Damage Response in ER Breast Cancer.MAGI1 可防止 ER 乳腺癌衰老并促进 DNA 损伤反应。
Cells. 2023 Jul 25;12(15):1929. doi: 10.3390/cells12151929.
3
Targeting the DNA Damage Response Machinery for Lung Cancer Treatment.靶向DNA损伤反应机制用于肺癌治疗
Pharmaceuticals (Basel). 2022 Nov 27;15(12):1475. doi: 10.3390/ph15121475.
4
DNA damage in cancer development: special implications in viral oncogenesis.癌症发展中的DNA损伤:对病毒致癌作用的特殊影响。
Am J Cancer Res. 2021 Aug 15;11(8):3956-3979. eCollection 2021.
5
Beta-Genus Human Papillomavirus 8 E6 Destabilizes the Host Genome by Promoting p300 Degradation.β属人乳头瘤病毒 8 型 E6 通过促进 p300 降解来破坏宿主基因组。
Viruses. 2021 Aug 21;13(8):1662. doi: 10.3390/v13081662.
6
Therapeutic Sequences in the Treatment of High-Risk Prostate Cancer: Paving the Way Towards Multimodal Tailored Approaches.高危前列腺癌治疗中的治疗顺序:为多模式个体化治疗方法铺平道路。
Front Oncol. 2021 Aug 4;11:732766. doi: 10.3389/fonc.2021.732766. eCollection 2021.
7
The SWI/SNF ATPase BRG1 stimulates DNA end resection and homologous recombination by reducing nucleosome density at DNA double strand breaks and by promoting the recruitment of the CtIP nuclease.SWI/SNF ATP 酶 BRG1 通过降低 DNA 双链断裂处核小体的密度,并促进 CtIP 核酸酶的募集,刺激 DNA 末端切除和同源重组。
Cell Cycle. 2020 Nov;19(22):3096-3114. doi: 10.1080/15384101.2020.1831256. Epub 2020 Oct 12.
8
Combining PARP Inhibition with Platinum, Ruthenium or Gold Complexes for Cancer Therapy.联合 PARP 抑制剂与铂、钌或金配合物用于癌症治疗。
ChemMedChem. 2020 Nov 18;15(22):2121-2135. doi: 10.1002/cmdc.202000391. Epub 2020 Sep 10.
9
Implementation of the Chick Chorioallantoic Membrane (CAM) Model in Radiation Biology and Experimental Radiation Oncology Research.鸡胚绒毛尿囊膜(CAM)模型在放射生物学和实验放射肿瘤学研究中的应用
Cancers (Basel). 2019 Oct 7;11(10):1499. doi: 10.3390/cancers11101499.
10
Nickel Carcinogenesis Mechanism: DNA Damage.镍致癌机制:DNA 损伤。
Int J Mol Sci. 2019 Sep 21;20(19):4690. doi: 10.3390/ijms20194690.

本文引用的文献

1
Improving efficacy of hyperthermia in oncology by exploiting biological mechanisms.通过利用生物学机制提高肿瘤热疗的疗效。
Int J Hyperthermia. 2016 Jun;32(4):446-54. doi: 10.3109/02656736.2016.1157216. Epub 2016 Apr 18.
2
Ovarian cancer: Status of homologous recombination pathway as a predictor of drug response.卵巢癌:同源重组途径作为药物反应预测指标的现状
Crit Rev Oncol Hematol. 2016 May;101:50-9. doi: 10.1016/j.critrevonc.2016.02.014. Epub 2016 Feb 27.
3
Potent and Selective Inhibitors of MTH1 Probe Its Role in Cancer Cell Survival.强效且选择性的 MTH1 抑制剂探究其在癌细胞存活中的作用。
J Med Chem. 2016 Mar 24;59(6):2346-61. doi: 10.1021/acs.jmedchem.5b01760. Epub 2016 Feb 16.
4
Tumor slice culture system to assess drug response of primary breast cancer.用于评估原发性乳腺癌药物反应的肿瘤切片培养系统
BMC Cancer. 2016 Feb 9;16:78. doi: 10.1186/s12885-016-2119-2.
5
Hallmarks of hyperthermia in driving the future of clinical hyperthermia as targeted therapy: translation into clinical application.热疗作为靶向治疗推动临床热疗未来发展的特征:转化为临床应用
Int J Hyperthermia. 2016;32(1):89-95. doi: 10.3109/02656736.2015.1119317. Epub 2016 Jan 24.
6
Capturing complex tumour biology in vitro: histological and molecular characterisation of precision cut slices.在体外捕捉复杂的肿瘤生物学:精密切片的组织学和分子特征分析
Sci Rep. 2015 Dec 9;5:17187. doi: 10.1038/srep17187.
7
DNA Damage Signalling and Repair Inhibitors: The Long-Sought-After Achilles' Heel of Cancer.DNA损伤信号传导与修复抑制剂:癌症长期以来一直寻觅的阿喀琉斯之踵。
Biomolecules. 2015 Nov 20;5(4):3204-59. doi: 10.3390/biom5043204.
8
Targeting the DNA Damage Response in Cancer.靶向癌症的 DNA 损伤反应。
Mol Cell. 2015 Nov 19;60(4):547-60. doi: 10.1016/j.molcel.2015.10.040.
9
Alternative end-joining repair pathways are the ultimate backup for abrogated classical non-homologous end-joining and homologous recombination repair: Implications for the formation of chromosome translocations.替代末端连接修复途径是经典非同源末端连接和同源重组修复被废除后的最终备用途径:对染色体易位形成的影响。
Mutat Res Genet Toxicol Environ Mutagen. 2015 Nov;793:166-75. doi: 10.1016/j.mrgentox.2015.07.001. Epub 2015 Jul 4.
10
Genome Integrity in Aging: Human Syndromes, Mouse Models, and Therapeutic Options.衰老中的基因组完整性:人类综合征、小鼠模型和治疗选择。
Annu Rev Pharmacol Toxicol. 2016;56:427-45. doi: 10.1146/annurev-pharmtox-010814-124316. Epub 2015 Oct 28.