• 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

解读组蛋白去乙酰化酶抑制剂的临床检测。

Interpreting clinical assays for histone deacetylase inhibitors.

机构信息

Laboratory of Bioactive Molecules, Institute of Chemistry, University of Nice - Sophia Antipolis, Parc Valrose, Nice, France;

出版信息

Cancer Manag Res. 2011;3:117-41. doi: 10.2147/CMR.S9661. Epub 2011 May 9.

DOI:10.2147/CMR.S9661
PMID:21625397
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3101110/
Abstract

As opposed to genetics, dealing with gene expressions by direct DNA sequence modifications, the term epigenetics applies to all the external influences that target the chromatin structure of cells with impact on gene expression unrelated to the sequence coding of DNA itself. In normal cells, epigenetics modulates gene expression through all development steps. When "imprinted" early by the environment, epigenetic changes influence the organism at an early stage and can be transmitted to the progeny. Together with DNA sequence alterations, DNA aberrant cytosine methylation and microRNA deregulation, epigenetic modifications participate in the malignant transformation of cells. Their reversible nature has led to the emergence of the promising field of epigenetic therapy. The efforts made to inhibit in particular the epigenetic enzyme family called histone deacetylases (HDACs) are described. HDAC inhibitors (HDACi) have been proposed as a viable clinical therapeutic approach for the treatment of leukemia and solid tumors, but also to a lesser degree for noncancerous diseases. Three epigenetic drugs are already arriving at the patient's bedside, and more than 100 clinical assays for HDACi are registered on the National Cancer Institute website. They explore the eventual additive benefits of combined therapies. In the context of the pleiotropic effects of HDAC isoforms, more specific HDACi and more informative screening tests are being developed for the benefit of the patients.

摘要

与直接通过 DNA 序列修饰来处理基因表达的遗传学不同,表观遗传学适用于所有针对细胞染色质结构的外部影响,这些影响会影响基因表达,而与 DNA 自身的编码序列无关。在正常细胞中,表观遗传学通过所有发育步骤来调节基因表达。当早期受到环境的“印记”时,表观遗传变化会在早期影响生物体,并可以传递给后代。与 DNA 序列改变、DNA 异常胞嘧啶甲基化和 microRNA 失调一起,表观遗传修饰参与了细胞的恶性转化。它们的可逆性质导致了有前途的表观遗传治疗领域的出现。描述了抑制特别是称为组蛋白去乙酰化酶 (HDAC) 的表观遗传酶家族的努力。HDAC 抑制剂 (HDACi) 已被提议作为治疗白血病和实体瘤的可行临床治疗方法,但在治疗非癌症疾病方面的效果也较小。三种表观遗传药物已经到达患者床边,并且在国立癌症研究所网站上注册了超过 100 种用于 HDACi 的临床检测。它们探索了联合治疗的潜在附加益处。在 HDAC 同工型的多效性效应的背景下,正在为患者的利益开发更特异的 HDACi 和更具信息量的筛选试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a0/3101110/b315169ada99/cmr-3-117f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a0/3101110/580e2504a3c7/cmr-3-117f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a0/3101110/ef2e59a6c94c/cmr-3-117f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a0/3101110/58464cecb01d/cmr-3-117f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a0/3101110/b315169ada99/cmr-3-117f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a0/3101110/580e2504a3c7/cmr-3-117f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a0/3101110/ef2e59a6c94c/cmr-3-117f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a0/3101110/58464cecb01d/cmr-3-117f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a0/3101110/b315169ada99/cmr-3-117f4.jpg

相似文献

1
Interpreting clinical assays for histone deacetylase inhibitors.解读组蛋白去乙酰化酶抑制剂的临床检测。
Cancer Manag Res. 2011;3:117-41. doi: 10.2147/CMR.S9661. Epub 2011 May 9.
2
Epigenetic therapy of cancer with histone deacetylase inhibitors.用组蛋白去乙酰化酶抑制剂进行癌症的表观遗传治疗。
J Cancer Res Ther. 2014 Jul-Sep;10(3):469-78. doi: 10.4103/0973-1482.137937.
3
Differential effects of class I isoform histone deacetylase depletion and enzymatic inhibition by belinostat or valproic acid in HeLa cells.I类亚型组蛋白去乙酰化酶缺失以及贝利司他或丙戊酸对HeLa细胞的酶抑制作用的差异效应
Mol Cancer. 2008 Sep 12;7:70. doi: 10.1186/1476-4598-7-70.
4
Histone Deacetylases and Histone Deacetylase Inhibitors in Neuroblastoma.神经母细胞瘤中的组蛋白去乙酰化酶和组蛋白去乙酰化酶抑制剂
Front Cell Dev Biol. 2020 Oct 7;8:578770. doi: 10.3389/fcell.2020.578770. eCollection 2020.
5
Histone deacetylases as targets in autoimmune and autoinflammatory diseases.组蛋白去乙酰化酶作为自身免疫和自身炎症性疾病的靶点。
Adv Immunol. 2020;147:1-59. doi: 10.1016/bs.ai.2020.06.001. Epub 2020 Jul 15.
6
Deacetylation of Histones and Non-histone Proteins in Inflammatory Diseases and Cancer Therapeutic Potential of Histone Deacetylase Inhibitors.炎症性疾病中组蛋白和非组蛋白的去乙酰化以及组蛋白去乙酰化酶抑制剂的癌症治疗潜力
Curr Genomics. 2023 Nov 22;24(3):136-145. doi: 10.2174/0113892029265046231011100327.
7
The emerging role of histone deacetylase (HDAC) inhibitors in urological cancers.组蛋白去乙酰化酶(HDAC)抑制剂在泌尿系统癌症中的新兴作用。
BJU Int. 2013 Apr;111(4):537-42. doi: 10.1111/j.1464-410X.2012.11647.x.
8
Combination Therapy With Histone Deacetylase Inhibitors (HDACi) for the Treatment of Cancer: Achieving the Full Therapeutic Potential of HDACi.组蛋白去乙酰化酶抑制剂(HDACi)联合疗法治疗癌症:实现HDACi的全部治疗潜力
Front Oncol. 2018 Mar 29;8:92. doi: 10.3389/fonc.2018.00092. eCollection 2018.
9
Epigenomics in stress tolerance of plants under the climate change.植物在气候变化下的应激耐受中的表观基因组学。
Mol Biol Rep. 2023 Jul;50(7):6201-6216. doi: 10.1007/s11033-023-08539-6. Epub 2023 Jun 9.
10
Epigenetic Regulation of TRAIL Signaling: Implication for Cancer Therapy.肿瘤坏死因子相关凋亡诱导配体(TRAIL)信号传导的表观遗传调控:对癌症治疗的意义
Cancers (Basel). 2019 Jun 19;11(6):850. doi: 10.3390/cancers11060850.

引用本文的文献

1
Epigenetic Drugs for Cancer and microRNAs: A Focus on Histone Deacetylase Inhibitors.用于癌症治疗的表观遗传药物与微小RNA:聚焦组蛋白去乙酰化酶抑制剂
Cancers (Basel). 2019 Oct 10;11(10):1530. doi: 10.3390/cancers11101530.
2
Quantifying Tip60 (Kat5) stratifies breast cancer.量化 Tip60(Kat5)可分层乳腺癌。
Sci Rep. 2019 Mar 7;9(1):3819. doi: 10.1038/s41598-019-40221-5.
3
The ROMP: A Powerful Approach to Synthesize Novel pH-Sensitive Nanoparticles for Tumor Therapy.ROMP:一种用于合成新型 pH 敏感纳米粒子进行肿瘤治疗的强大方法。

本文引用的文献

1
Histone deacetylase inhibitor PCI-24781 enhances chemotherapy-induced apoptosis in multidrug-resistant sarcoma cell lines.组蛋白去乙酰化酶抑制剂 PCI-24781 增强多药耐药肉瘤细胞系的化疗诱导凋亡。
Anticancer Res. 2011 Apr;31(4):1115-23.
2
Chemoproteomics profiling of HDAC inhibitors reveals selective targeting of HDAC complexes.化学生物学蛋白质组学分析组蛋白去乙酰化酶抑制剂揭示了对 HDAC 复合物的选择性靶向。
Nat Biotechnol. 2011 Mar;29(3):255-65. doi: 10.1038/nbt.1759. Epub 2011 Jan 23.
3
Histone deacetylases 9 and 10 are required for homologous recombination.
Biomolecules. 2019 Feb 12;9(2):60. doi: 10.3390/biom9020060.
4
Histone deacetylases as targets for antitrypanosomal drugs.组蛋白去乙酰化酶作为抗锥虫药物的靶点
Future Sci OA. 2018 Jul 27;4(8):FSO325. doi: 10.4155/fsoa-2018-0037. eCollection 2018 Sep.
5
Assessment of new HDAC inhibitors for immunotherapy of malignant pleural mesothelioma.评估新型 HDAC 抑制剂在恶性胸膜间皮瘤免疫治疗中的作用。
Clin Epigenetics. 2018 Jun 18;10:79. doi: 10.1186/s13148-018-0517-9. eCollection 2018.
6
A phase 1 dose-escalation study of the oral histone deacetylase inhibitor abexinostat in combination with standard hypofractionated radiotherapy in advanced solid tumors.口服组蛋白去乙酰化酶抑制剂阿贝西诺斯特联合标准低分割放疗用于晚期实体瘤的1期剂量递增研究。
Oncotarget. 2016 Dec 24;8(34):56199-56209. doi: 10.18632/oncotarget.14147. eCollection 2017 Aug 22.
7
Targeting cancer using KAT inhibitors to mimic lethal knockouts.使用KAT抑制剂靶向癌症以模拟致死性基因敲除。
Biochem Soc Trans. 2016 Aug 15;44(4):979-86. doi: 10.1042/BST20160081.
8
LTR12 promoter activation in a broad range of human tumor cells by HDAC inhibition.通过抑制组蛋白去乙酰化酶(HDAC)在多种人类肿瘤细胞中激活LTR12启动子
Oncotarget. 2016 Jun 7;7(23):33484-97. doi: 10.18632/oncotarget.9255.
9
Identification of histone deacetylase inhibitors with benzoylhydrazide scaffold that selectively inhibit class I histone deacetylases.具有苯甲酰肼支架的组蛋白脱乙酰酶抑制剂的鉴定,该抑制剂可选择性抑制I类组蛋白脱乙酰酶。
Chem Biol. 2015 Feb 19;22(2):273-84. doi: 10.1016/j.chembiol.2014.12.015.
10
PRMT1 arginine methyltransferase accumulates in cytoplasmic bodies that respond to selective inhibition and DNA damage.蛋白质精氨酸甲基转移酶1(PRMT1)在对选择性抑制和DNA损伤作出反应的胞质小体中积累。
Eur J Histochem. 2014 May 2;58(2):2389. doi: 10.4081/ejh.2014.2389.
组蛋白去乙酰化酶 9 和 10 对于同源重组是必需的。
J Biol Chem. 2011 Mar 11;286(10):7722-7726. doi: 10.1074/jbc.C110.194233. Epub 2011 Jan 18.
4
Dynamic interplay between histone H3 modifications and protein interpreters: emerging evidence for a "histone language".组蛋白 H3 修饰与蛋白解读器之间的动态相互作用:“组蛋白语言”的新证据
Chembiochem. 2011 Jan 24;12(2):299-307. doi: 10.1002/cbic.201000474. Epub 2010 Oct 29.
5
A review of the sirtuin system, its clinical implications, and the potential role of dietary activators like resveratrol: part 1.沉默调节蛋白系统综述、其临床意义以及白藜芦醇等膳食激活剂的潜在作用:第1部分。
Altern Med Rev. 2010 Sep;15(3):245-63.
6
Global turnover of histone post-translational modifications and variants in human cells.人类细胞中组蛋白翻译后修饰和变体的全球周转率。
Epigenetics Chromatin. 2010 Dec 6;3(1):22. doi: 10.1186/1756-8935-3-22.
7
Emerging role of epigenetic therapies in cutaneous T-cell  lymphomas.表观遗传学疗法在皮肤 T 细胞淋巴瘤中的新作用。
Expert Rev Hematol. 2010 Apr;3(2):187-203. doi: 10.1586/ehm.10.9.
8
Epigenetics and miRNAs in human cancer.人类癌症中的表观遗传学和 miRNA。
Adv Genet. 2010;70:87-99. doi: 10.1016/B978-0-12-380866-0.60004-6.
9
N(epsilon)-Modified lysine containing inhibitors for SIRT1 and SIRT2.N(epsilon)-修饰的赖氨酸含有 SIRT1 和 SIRT2 的抑制剂。
Bioorg Med Chem. 2010 Aug 1;18(15):5616-25. doi: 10.1016/j.bmc.2010.06.035. Epub 2010 Jun 17.
10
Histone deacetylase 3 depletion in osteo/chondroprogenitor cells decreases bone density and increases marrow fat.成骨/软骨祖细胞中组蛋白去乙酰化酶 3 的耗竭降低骨密度并增加骨髓脂肪。
PLoS One. 2010 Jul 9;5(7):e11492. doi: 10.1371/journal.pone.0011492.