• 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
Targeting RNA helicases in cancer: The translation trap.靶向癌症中的 RNA 解旋酶:翻译陷阱。
Biochim Biophys Acta Rev Cancer. 2017 Dec;1868(2):510-520. doi: 10.1016/j.bbcan.2017.09.006. Epub 2017 Sep 28.
2
Transcriptome-wide characterization of the eIF4A signature highlights plasticity in translation regulation.全转录组范围内对真核起始因子4A(eIF4A)特征的表征突出了翻译调控中的可塑性。
Genome Biol. 2014;15(10):476. doi: 10.1186/s13059-014-0476-1.
3
eIF4B stimulates translation of long mRNAs with structured 5' UTRs and low closed-loop potential but weak dependence on eIF4G.真核生物翻译起始因子4B(eIF4B)可刺激具有结构化5'非翻译区(UTR)且闭环潜力低但对eIF4G依赖性弱的长链信使核糖核酸(mRNA)的翻译。
Proc Natl Acad Sci U S A. 2016 Sep 20;113(38):10464-72. doi: 10.1073/pnas.1612398113. Epub 2016 Sep 6.
4
Selective targeting of the DEAD-box RNA helicase eukaryotic initiation factor (eIF) 4A by natural products.天然产物对 DEAD-box RNA 解旋酶真核起始因子 (eIF) 4A 的选择性靶向作用。
Nat Prod Rep. 2020 May 1;37(5):609-616. doi: 10.1039/c9np00052f. Epub 2019 Nov 29.
5
Rocaglates convert DEAD-box protein eIF4A into a sequence-selective translational repressor.罗卡类化合物将DEAD盒蛋白eIF4A转化为序列选择性翻译阻遏物。
Nature. 2016 Jun 23;534(7608):558-61. doi: 10.1038/nature17978. Epub 2016 Jun 15.
6
Inhibiting CARD11 translation during BCR activation by targeting the eIF4A RNA helicase.通过靶向真核翻译起始因子4A(eIF4A)RNA解旋酶在B细胞受体(BCR)激活过程中抑制CARD11的翻译。
Blood. 2014 Dec 11;124(25):3758-67. doi: 10.1182/blood-2014-07-589689. Epub 2014 Oct 15.
7
Monitoring RNA restructuring in a human cell-free extract reveals eIF4A-dependent and eIF4A-independent unwinding activity.在人源无细胞提取物中监测 RNA 重排揭示了 eIF4A 依赖性和 eIF4A 非依赖性解旋活性。
J Biol Chem. 2023 Jul;299(7):104936. doi: 10.1016/j.jbc.2023.104936. Epub 2023 Jun 17.
8
Human DDX3 functions in translation and interacts with the translation initiation factor eIF3.人类DDX3在翻译过程中发挥作用,并与翻译起始因子eIF3相互作用。
Nucleic Acids Res. 2008 Aug;36(14):4708-18. doi: 10.1093/nar/gkn454. Epub 2008 Jul 15.
9
Yeast RNA helicases of the DEAD-box family involved in translation initiation.参与翻译起始的DEAD-box家族酵母RNA解旋酶。
Biol Cell. 2003 May-Jun;95(3-4):157-67. doi: 10.1016/s0248-4900(03)00032-7.
10
Targeting the eIF4A RNA helicase as an anti-neoplastic approach.将真核生物翻译起始因子4A(eIF4A)RNA解旋酶作为一种抗肿瘤方法。
Biochim Biophys Acta. 2015 Jul;1849(7):781-91. doi: 10.1016/j.bbagrm.2014.09.006. Epub 2014 Sep 16.

引用本文的文献

1
DDX10 Exacerbates Exosomal PD-L1-Dependent T Cell Exhaustion via Phase Separation of Rab27b in Oral Squamous Cell Carcinoma.DDX10通过口腔鳞状细胞癌中Rab27b的相分离加剧外泌体PD-L1依赖性T细胞耗竭。
Research (Wash D C). 2025 May 9;8:0697. doi: 10.34133/research.0697. eCollection 2025.
2
Small-molecule RNA therapeutics to target prostate cancer.靶向前列腺癌的小分子RNA疗法。
Cancer Cell. 2025 May 12;43(5):841-855.e8. doi: 10.1016/j.ccell.2025.02.027. Epub 2025 Mar 20.
3
Structural Basis for the Improved RNA Clamping of Amidino-Rocaglates to eIF4A1.脒基-罗卡酯对eIF4A1增强RNA钳制作用的结构基础
ACS Omega. 2025 Feb 10;10(6):5795-5808. doi: 10.1021/acsomega.4c09421. eCollection 2025 Feb 18.
4
DDX19A promotes gastric cancer cell proliferation and migration by activating the PI3K/AKT pathway.DDX19A通过激活PI3K/AKT信号通路促进胃癌细胞的增殖和迁移。
Cancer Cell Int. 2024 Aug 3;24(1):272. doi: 10.1186/s12935-024-03448-5.
5
Envafolimab Inhibits the Growth of Gastric Cancer Cells with Low PD-L1 Expression through the DDX20/NF-κB/TNF-α Signaling Pathway.恩瓦利单抗通过DDX20/核因子-κB/肿瘤坏死因子-α信号通路抑制低程序性死亡配体1表达的胃癌细胞生长。
Curr Cancer Drug Targets. 2025;25(6):648-664. doi: 10.2174/0115680096314855240619181909.
6
Post-transcriptional regulation of DEAD-box RNA helicases in hematopoietic malignancies.造血系统恶性肿瘤中DEAD盒RNA解旋酶的转录后调控
Genes Dis. 2024 Feb 28;11(5):101252. doi: 10.1016/j.gendis.2024.101252. eCollection 2024 Sep.
7
Facilitates the Tumorigenesis of Lung Adenocarcinoma by Promoting Cell Cycle Progression through the Upregulation of CDK4.通过上调 CDK4 促进细胞周期进程促进肺腺癌的肿瘤发生。
Int J Mol Sci. 2024 May 1;25(9):4953. doi: 10.3390/ijms25094953.
8
Surface Proteome of Extracellular Vesicles and Correlation Analysis Reveal Breast Cancer Biomarkers.细胞外囊泡表面蛋白质组及相关性分析揭示乳腺癌生物标志物
Cancers (Basel). 2024 Jan 25;16(3):520. doi: 10.3390/cancers16030520.
9
A co-regulatory network of and related to immune infiltration for early-stage colorectal cancer in silico and in vitro.用于早期结直肠癌的与免疫浸润相关的 和 的共调控网络的计算机模拟及体外研究 。 你提供的原文似乎不完整,“和”的部分内容缺失。
Am J Cancer Res. 2023 Nov 15;13(11):5271-5288. eCollection 2023.
10
Identification of DHX40 as a candidate susceptibility gene for colorectal and hematological neoplasia.鉴定DHX40作为结直肠癌和血液系统肿瘤的候选易感基因。
Leukemia. 2023 Nov;37(11):2301-2305. doi: 10.1038/s41375-023-02021-9. Epub 2023 Sep 11.

本文引用的文献

1
Targeting mitochondrial translation by inhibiting DDX3: a novel radiosensitization strategy for cancer treatment.通过抑制 DDX3 靶向线粒体翻译:一种用于癌症治疗的新型放射增敏策略。
Oncogene. 2018 Jan 4;37(1):63-74. doi: 10.1038/onc.2017.308. Epub 2017 Sep 4.
2
Combination treatment using DDX3 and PARP inhibitors induces synthetic lethality in BRCA1-proficient breast cancer.使用DDX3和PARP抑制剂的联合治疗在BRCA1功能正常的乳腺癌中诱导合成致死效应。
Med Oncol. 2017 Mar;34(3):33. doi: 10.1007/s12032-017-0889-2. Epub 2017 Jan 30.
3
Tumor-suppressor genes that escape from X-inactivation contribute to cancer sex bias.逃避X染色体失活的肿瘤抑制基因导致癌症的性别差异。
Nat Genet. 2017 Jan;49(1):10-16. doi: 10.1038/ng.3726. Epub 2016 Nov 21.
4
RK-33 Radiosensitizes Prostate Cancer Cells by Blocking the RNA Helicase DDX3.RK-33通过阻断RNA解旋酶DDX3使前列腺癌细胞对放疗增敏。
Cancer Res. 2016 Nov 1;76(21):6340-6350. doi: 10.1158/0008-5472.CAN-16-0440. Epub 2016 Sep 12.
5
Translation Initiation Factors: Reprogramming Protein Synthesis in Cancer.翻译起始因子:在癌症中重新编程蛋白质合成。
Trends Cell Biol. 2016 Dec;26(12):918-933. doi: 10.1016/j.tcb.2016.06.005. Epub 2016 Jul 15.
6
Rocaglates convert DEAD-box protein eIF4A into a sequence-selective translational repressor.罗卡类化合物将DEAD盒蛋白eIF4A转化为序列选择性翻译阻遏物。
Nature. 2016 Jun 23;534(7608):558-61. doi: 10.1038/nature17978. Epub 2016 Jun 15.
7
CRISPR-Mediated Drug-Target Validation Reveals Selective Pharmacological Inhibition of the RNA Helicase, eIF4A.CRISPR介导的药物靶点验证揭示了RNA解旋酶eIF4A的选择性药理抑制作用。
Cell Rep. 2016 Jun 14;15(11):2340-7. doi: 10.1016/j.celrep.2016.05.005. Epub 2016 May 26.
8
Cancer-associated DDX3X mutations drive stress granule assembly and impair global translation.癌症相关的DDX3X突变驱动应激颗粒组装并损害整体翻译。
Sci Rep. 2016 May 16;6:25996. doi: 10.1038/srep25996.
9
Human DDX3 protein is a valuable target to develop broad spectrum antiviral agents.人类DDX3蛋白是开发广谱抗病毒药物的一个有价值的靶点。
Proc Natl Acad Sci U S A. 2016 May 10;113(19):5388-93. doi: 10.1073/pnas.1522987113. Epub 2016 Apr 26.
10
New frontiers in translational control of the cancer genome.癌症基因组翻译控制的新前沿。
Nat Rev Cancer. 2016 Apr 26;16(5):288-304. doi: 10.1038/nrc.2016.27.

靶向癌症中的 RNA 解旋酶:翻译陷阱。

Targeting RNA helicases in cancer: The translation trap.

机构信息

Department of Radiology and Radiological Sciences, Johns Hopkins University, School of Medicine, Baltimore, MD, USA; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.

Department of Radiology and Radiological Sciences, Johns Hopkins University, School of Medicine, Baltimore, MD, USA; Department of Oncology, Johns Hopkins University, School of Medicine, MD, USA.

出版信息

Biochim Biophys Acta Rev Cancer. 2017 Dec;1868(2):510-520. doi: 10.1016/j.bbcan.2017.09.006. Epub 2017 Sep 28.

DOI:10.1016/j.bbcan.2017.09.006
PMID:28965870
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5675762/
Abstract

Cancer cells are reliant on the cellular translational machinery for both global elevation of protein synthesis and the translation of specific mRNAs that promote tumor cell survival. Targeting translational control in cancer is therefore increasingly recognized as a promising therapeutic strategy. In this regard, DEAD/H box RNA helicases are a very interesting group of proteins, with several family members regulating mRNA translation in cancer cells. In this review, we delineate the mechanisms by which DEAD/H box proteins modulate oncogenic translation and how inhibition of these RNA helicases can be exploited for anti-cancer therapeutics.

摘要

癌细胞依赖细胞翻译机制来提高蛋白质合成的整体水平,并翻译特定的促进肿瘤细胞存活的 mRNA。因此,靶向癌症中的翻译控制被认为是一种很有前途的治疗策略。在这方面,DEAD/H 盒 RNA 解旋酶是一组非常有趣的蛋白质,有几个家族成员调节癌细胞中的 mRNA 翻译。在这篇综述中,我们阐述了 DEAD/H 盒蛋白调节致癌翻译的机制,以及如何利用这些 RNA 解旋酶的抑制作用来进行抗癌治疗。