• 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

相似文献

1
CRISPR/Cas9: From Genome Engineering to Cancer Drug Discovery.CRISPR/Cas9:从基因组工程到癌症药物发现
Trends Cancer. 2016 Jun;2(6):313-324. doi: 10.1016/j.trecan.2016.05.001.
2
The role of the CRISPR-Cas system in cancer drug development: Mechanisms of action and therapy.CRISPR-Cas 系统在癌症药物开发中的作用:作用机制与治疗。
Biotechnol J. 2022 Jul;17(7):e2100468. doi: 10.1002/biot.202100468. Epub 2022 Feb 20.
3
A Perspective on the Future of High-Throughput RNAi Screening: Will CRISPR Cut Out the Competition or Can RNAi Help Guide the Way?高通量RNA干扰筛选的未来展望:CRISPR会脱颖而出还是RNA干扰能指引方向?
J Biomol Screen. 2015 Sep;20(8):1040-51. doi: 10.1177/1087057115590069. Epub 2015 Jun 5.
4
Use of CRISPR/Cas9 gene-editing tools for developing models in drug discovery.使用 CRISPR/Cas9 基因编辑工具开发药物发现模型。
Drug Discov Today. 2018 Mar;23(3):519-533. doi: 10.1016/j.drudis.2018.01.014. Epub 2018 Jan 8.
5
Advances in CRISPR-Cas9 genome engineering: lessons learned from RNA interference.CRISPR-Cas9基因组工程的进展:从RNA干扰中汲取的经验教训。
Nucleic Acids Res. 2015 Apr 20;43(7):3407-19. doi: 10.1093/nar/gkv226. Epub 2015 Mar 23.
6
A comprehensive overview of CRISPR/Cas 9 technology and application thereof in drug discovery.CRISPR/Cas9 技术概述及其在药物发现中的应用
J Cell Biochem. 2022 Oct;123(10):1674-1698. doi: 10.1002/jcb.30329. Epub 2022 Sep 21.
7
CRISPR-Cas system: a powerful tool for genome engineering.CRISPR-Cas 系统:一种强大的基因组工程工具。
Plant Mol Biol. 2014 Jun;85(3):209-18. doi: 10.1007/s11103-014-0188-7. Epub 2014 Mar 18.
8
[CRISPR/Cas systems in genome engineering of bacteriophages].[噬菌体基因组工程中的CRISPR/Cas系统]
Yi Chuan. 2018 May 20;40(5):378-389. doi: 10.16288/j.yczz.17-419.
9
CRISPR/Cas technologies for cancer drug discovery and treatment.用于癌症药物发现与治疗的CRISPR/Cas技术。
Trends Pharmacol Sci. 2025 May;46(5):437-452. doi: 10.1016/j.tips.2025.02.009. Epub 2025 Mar 24.
10
How specific is CRISPR/Cas9 really?CRISPR/Cas9究竟有多特异性?
Curr Opin Chem Biol. 2015 Dec;29:72-8. doi: 10.1016/j.cbpa.2015.10.001. Epub 2015 Oct 24.

引用本文的文献

1
Predicting tumour resistance to paclitaxel and carboplatin utilising genome-wide screening in haploid human embryonic stem cells.利用单倍体人类胚胎干细胞的全基因组筛选预测肿瘤对紫杉醇和卡铂的耐药性。
Cell Prolif. 2025 Mar;58(3):e13771. doi: 10.1111/cpr.13771. Epub 2024 Nov 10.
2
Small molecule induced STING degradation facilitated by the HECT ligase HERC4.小分子诱导的 STING 降解由 HECT 连接酶 HERC4 介导。
Nat Commun. 2024 May 29;15(1):4584. doi: 10.1038/s41467-024-48922-w.
3
Therapeutic potential of adiponectin in prediabetes: strategies, challenges, and future directions.脂联素在糖尿病前期的治疗潜力:策略、挑战及未来方向
Ther Adv Endocrinol Metab. 2024 Jan 18;15:20420188231222371. doi: 10.1177/20420188231222371. eCollection 2024.
4
Rewiring Drug Research and Development through Human Data-Driven Discovery (HD).通过人类数据驱动发现(HD)重塑药物研发
Pharmaceutics. 2023 Jun 7;15(6):1673. doi: 10.3390/pharmaceutics15061673.
5
CRISPR-Cas9-mediated gene therapy in lung cancer.CRISPR-Cas9介导的肺癌基因治疗。
Clin Transl Oncol. 2023 May;25(5):1156-1166. doi: 10.1007/s12094-022-03039-8. Epub 2022 Dec 10.
6
A Genome-Wide Screen Identifies PDPK1 as a Target to Enhance the Efficacy of MEK1/2 Inhibitors in NRAS Mutant Melanoma.全基因组筛选鉴定出 PDPK1 是增强 MEK1/2 抑制剂在NRAS 突变型黑色素瘤中的疗效的靶点。
Cancer Res. 2022 Jul 18;82(14):2625-2639. doi: 10.1158/0008-5472.CAN-21-3217.
7
Recent trends in miRNA therapeutics and the application of plant miRNA for prevention and treatment of human diseases.微小RNA疗法的最新趋势以及植物微小RNA在人类疾病预防和治疗中的应用。
Futur J Pharm Sci. 2022;8(1):24. doi: 10.1186/s43094-022-00413-9. Epub 2022 Apr 1.
8
Integrated genome and tissue engineering enables screening of cancer vulnerabilities in physiologically relevant perfusable ex vivo cultures.整体基因组与组织工程使得在生理相关可灌注的离体培养物中筛选癌症脆弱性成为可能。
Biomaterials. 2022 Jan;280:121276. doi: 10.1016/j.biomaterials.2021.121276. Epub 2021 Dec 2.
9
Targeting "undruggable" c-Myc protein by synthetic lethality.通过合成致死作用靶向“不可成药”的 c-Myc 蛋白。
Front Med. 2021 Aug;15(4):541-550. doi: 10.1007/s11684-020-0780-y. Epub 2021 Mar 4.
10
Drug Combination in Cancer Treatment-From Cocktails to Conjugated Combinations.癌症治疗中的药物联合——从鸡尾酒疗法到共轭组合疗法
Cancers (Basel). 2021 Feb 7;13(4):669. doi: 10.3390/cancers13040669.

本文引用的文献

1
The ORFeome Collaboration: a genome-scale human ORF-clone resource.开放阅读框组合作项目:一个基因组规模的人类开放阅读框克隆资源库。
Nat Methods. 2016 Mar;13(3):191-2. doi: 10.1038/nmeth.3776.
2
Optimized sgRNA design to maximize activity and minimize off-target effects of CRISPR-Cas9.优化sgRNA设计以最大化CRISPR-Cas9的活性并最小化脱靶效应。
Nat Biotechnol. 2016 Feb;34(2):184-191. doi: 10.1038/nbt.3437. Epub 2016 Jan 18.
3
CCAT1 is an enhancer-templated RNA that predicts BET sensitivity in colorectal cancer.CCAT1是一种增强子模板化RNA,可预测结直肠癌对BET蛋白的敏感性。
J Clin Invest. 2016 Feb;126(2):639-52. doi: 10.1172/JCI83265. Epub 2016 Jan 11.
4
High-fidelity CRISPR-Cas9 nucleases with no detectable genome-wide off-target effects.具有不可检测的全基因组脱靶效应的高保真CRISPR-Cas9核酸酶。
Nature. 2016 Jan 28;529(7587):490-5. doi: 10.1038/nature16526. Epub 2016 Jan 6.
5
In vivo gene editing in dystrophic mouse muscle and muscle stem cells.营养不良小鼠肌肉和肌肉干细胞中的体内基因编辑。
Science. 2016 Jan 22;351(6271):407-411. doi: 10.1126/science.aad5177. Epub 2015 Dec 31.
6
In vivo genome editing improves muscle function in a mouse model of Duchenne muscular dystrophy.体内基因组编辑改善了杜兴氏肌肉营养不良小鼠模型的肌肉功能。
Science. 2016 Jan 22;351(6271):403-7. doi: 10.1126/science.aad5143. Epub 2015 Dec 31.
7
Postnatal genome editing partially restores dystrophin expression in a mouse model of muscular dystrophy.产后基因编辑可部分恢复肌营养不良小鼠模型中的肌营养不良蛋白表达。
Science. 2016 Jan 22;351(6271):400-3. doi: 10.1126/science.aad5725. Epub 2015 Dec 31.
8
Beyond editing: repurposing CRISPR-Cas9 for precision genome regulation and interrogation.超越编辑:重新利用CRISPR-Cas9进行精准基因组调控与探究。
Nat Rev Mol Cell Biol. 2016 Jan;17(1):5-15. doi: 10.1038/nrm.2015.2. Epub 2015 Dec 16.
9
Rationally engineered Cas9 nucleases with improved specificity.具有更高特异性的理性设计的Cas9核酸酶。
Science. 2016 Jan 1;351(6268):84-8. doi: 10.1126/science.aad5227. Epub 2015 Dec 1.
10
High-Resolution CRISPR Screens Reveal Fitness Genes and Genotype-Specific Cancer Liabilities.高分辨率 CRISPR 筛选揭示了适应性基因和基因型特异性的癌症易感性。
Cell. 2015 Dec 3;163(6):1515-26. doi: 10.1016/j.cell.2015.11.015. Epub 2015 Nov 25.

CRISPR/Cas9:从基因组工程到癌症药物发现

CRISPR/Cas9: From Genome Engineering to Cancer Drug Discovery.

作者信息

Luo Ji

机构信息

Laboratory of Cancer Biology and Genomics, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20814, USA.

出版信息

Trends Cancer. 2016 Jun;2(6):313-324. doi: 10.1016/j.trecan.2016.05.001.

DOI:10.1016/j.trecan.2016.05.001
PMID:28603775
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5461962/
Abstract

Advances in translational research are often driven by new technologies. The advent of microarrays, next-generation sequencing, proteomics and RNA interference (RNAi) have led to breakthroughs in our understanding of the mechanisms of cancer and the discovery of new cancer drug targets. The discovery of the bacterial clustered regularly interspaced palindromic repeat (CRISPR) system and its subsequent adaptation as a tool for mammalian genome engineering has opened up new avenues for functional genomics studies. This review will focus on the utility of CRISPR in the context of cancer drug target discovery.

摘要

转化医学研究的进展往往由新技术推动。微阵列、新一代测序、蛋白质组学和RNA干扰(RNAi)的出现,使我们在理解癌症机制和发现新的癌症药物靶点方面取得了突破。细菌成簇规律间隔短回文重复序列(CRISPR)系统的发现及其随后作为哺乳动物基因组工程工具的应用,为功能基因组学研究开辟了新途径。本综述将聚焦CRISPR在癌症药物靶点发现方面的应用。