• 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

癌症表观基因组的药物靶向治疗。

Pharmacological targeting of the cancer epigenome.

机构信息

Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.

Broad Institute of MIT and Harvard, Cambridge, MA, USA.

出版信息

Nat Cancer. 2024 Jun;5(6):844-865. doi: 10.1038/s43018-024-00777-2. Epub 2024 Jun 27.

DOI:10.1038/s43018-024-00777-2
PMID:38937652
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11936478/
Abstract

Epigenetic dysregulation is increasingly appreciated as a hallmark of cancer, including disease initiation, maintenance and therapy resistance. As a result, there have been advances in the development and evaluation of epigenetic therapies for cancer, revealing substantial promise but also challenges. Three epigenetic inhibitor classes are approved in the USA, and many more are currently undergoing clinical investigation. In this Review, we discuss recent developments for each epigenetic drug class and their implications for therapy, as well as highlight new insights into the role of epigenetics in cancer.

摘要

表观遗传失调越来越被认为是癌症的一个标志,包括疾病的起始、维持和治疗抵抗。因此,在开发和评估癌症的表观遗传学治疗方法方面取得了进展,显示出了很大的希望,但也带来了挑战。在美国,有三种表观遗传抑制剂类药物获得批准,还有更多的药物正在进行临床研究。在这篇综述中,我们讨论了每一种表观遗传药物类别的最新进展及其对治疗的意义,并强调了对癌症中表观遗传学作用的新认识。

相似文献

1
Pharmacological targeting of the cancer epigenome.癌症表观基因组的药物靶向治疗。
Nat Cancer. 2024 Jun;5(6):844-865. doi: 10.1038/s43018-024-00777-2. Epub 2024 Jun 27.
2
New clinical developments in histone deacetylase inhibitors for epigenetic therapy of cancer.组蛋白去乙酰化酶抑制剂在癌症表观遗传学治疗中的新临床进展。
J Hematol Oncol. 2009 Jun 1;2:22. doi: 10.1186/1756-8722-2-22.
3
[Targeted epigenetic therapy of cancer. Achievements and perspectives].[癌症的靶向表观遗传治疗。成就与展望]
Cir Cir. 2012 Sep-Oct;80(5):470-80.
4
Predicting response to epigenetic therapy.预测表观遗传学治疗的反应。
J Clin Invest. 2014 Jan;124(1):47-55. doi: 10.1172/JCI69737. Epub 2014 Jan 2.
5
Epigenetics and oncology.表观遗传学与肿瘤学
Pharmacotherapy. 2014 May;34(5):495-505. doi: 10.1002/phar.1408. Epub 2014 Mar 11.
6
Advances in Epigenetic Therapeutics for Breast Cancer.乳腺癌表观遗传学治疗的进展。
Adv Exp Med Biol. 2024;1465:89-97. doi: 10.1007/978-3-031-66686-5_6.
7
Human DNA (cytosine-5)-methyltransferases: a functional and structural perspective for epigenetic cancer therapy.人类DNA(胞嘧啶-5)-甲基转移酶:表观遗传癌症治疗的功能与结构视角
Biochimie. 2017 Aug;139:137-147. doi: 10.1016/j.biochi.2017.06.003. Epub 2017 Jun 6.
8
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.
9
Epigenetic therapy for solid tumors: from bench science to clinical trials.实体瘤的表观遗传学治疗:从基础科学到临床试验。
Epigenomics. 2015;7(2):215-35. doi: 10.2217/epi.14.73.
10
Epigenetic drugs take on cancer.表观遗传药物对抗癌症。
Science. 2010 Oct 29;330(6004):576-8. doi: 10.1126/science.330.6004.576.

引用本文的文献

1
Research progress on NAT10-mediated acetylation in normal development and disease.NAT10介导的乙酰化在正常发育和疾病中的研究进展
Front Cell Dev Biol. 2025 Aug 13;13:1623276. doi: 10.3389/fcell.2025.1623276. eCollection 2025.
2
The ESRP1 promoter reporter can function as an in vivo sensor of DNA methyltransferase inhibition.ESRP1启动子报告基因可作为DNA甲基转移酶抑制作用的体内传感器。
BMC Biotechnol. 2025 Aug 27;25(1):90. doi: 10.1186/s12896-025-01031-y.
3
Valproic acid improves the efficacy of oxaliplatin/fluoropyrimidine-based chemotherapy by targeting cancer stem cell via β-Catenin modulation in colorectal cancer.

本文引用的文献

1
Defining the condensate landscape of fusion oncoproteins.定义融合癌蛋白的凝聚景观。
Nat Commun. 2023 Sep 28;14(1):6008. doi: 10.1038/s41467-023-41655-2.
2
CRISPR-ChIP reveals selective regulation of H3K79me2 by Menin in MLL leukemia.CRISPR-ChIP 揭示 Menin 对 MLL 白血病中 H3K79me2 的选择性调控。
Nat Struct Mol Biol. 2023 Oct;30(10):1592-1606. doi: 10.1038/s41594-023-01087-4. Epub 2023 Sep 7.
3
Collateral lethality between HDAC1 and HDAC2 exploits cancer-specific NuRD complex vulnerabilities.HDAC1 和 HDAC2 之间的附带致死作用利用了癌症特异性 NuRD 复合物的脆弱性。
丙戊酸通过调节β-连环蛋白靶向癌症干细胞,提高了奥沙利铂/氟嘧啶化疗方案在结直肠癌治疗中的疗效。
Cell Death Dis. 2025 Aug 1;16(1):583. doi: 10.1038/s41419-025-07902-8.
4
Emerging role of SETD2 in the development and function of immune cells.SETD2在免疫细胞发育和功能中的新作用。
Genes Dis. 2025 Apr 3;12(6):101622. doi: 10.1016/j.gendis.2025.101622. eCollection 2025 Nov.
5
Integrative Analysis Reveals the Prognostic Effects of Epigenetic Regulators in Bladder Cancer.综合分析揭示表观遗传调控因子在膀胱癌中的预后作用。
Cancer Med. 2025 Jul;14(14):e71057. doi: 10.1002/cam4.71057.
6
EZH2 inhibitor SHR2554 enhances the anti-tumor efficacy of HDAC inhibitor Chidamide through STAT1 in T-cell lymphoma.EZH2抑制剂SHR2554通过STAT1增强HDAC抑制剂西达本胺在T细胞淋巴瘤中的抗肿瘤疗效。
Cell Death Dis. 2025 Jul 14;16(1):522. doi: 10.1038/s41419-025-07775-x.
7
HDAC1/2-mediated deacetylation of KLF9 promotes the malignant progression of nasopharyngeal carcinoma via CDH17.HDAC1/2介导的KLF9去乙酰化通过CDH17促进鼻咽癌的恶性进展。
Oncogene. 2025 Jul 4. doi: 10.1038/s41388-025-03471-4.
8
Oncogenic viruses rewire the epigenome in human cancer.致癌病毒在人类癌症中重塑表观基因组。
Front Cell Infect Microbiol. 2025 Jun 10;15:1617198. doi: 10.3389/fcimb.2025.1617198. eCollection 2025.
9
Nuclear-localized metabolic enzymes: emerging key players in tumor epigenetic regulation.核定位代谢酶:肿瘤表观遗传调控中新兴的关键因子
Mol Cell Biochem. 2025 May 28. doi: 10.1007/s11010-025-05316-w.
10
The evolving landscape of epigenetic target molecules and therapies in myeloid cancers: focus on acute myeloid leukemia and myeloproliferative neoplasms.髓系癌症中表观遗传靶分子与疗法的演变格局:聚焦急性髓系白血病和骨髓增殖性肿瘤
Leukemia. 2025 May 15. doi: 10.1038/s41375-025-02639-x.
Nat Struct Mol Biol. 2023 Aug;30(8):1160-1171. doi: 10.1038/s41594-023-01041-4. Epub 2023 Jul 24.
4
Diverse clonal fates emerge upon drug treatment of homogeneous cancer cells.药物治疗同质癌细胞会出现不同的克隆命运。
Nature. 2023 Aug;620(7974):651-659. doi: 10.1038/s41586-023-06342-8. Epub 2023 Jul 19.
5
Discovery of Exceptionally Potent, Selective, and Efficacious PROTAC Degraders of CBP and p300 Proteins.发现具有超强效力、高选择性且高效的CBP和p300蛋白PROTAC降解剂。
J Med Chem. 2023 Jun 22;66(12):8178-8199. doi: 10.1021/acs.jmedchem.3c00492. Epub 2023 Jun 5.
6
The menin inhibitor revumenib in KMT2A-rearranged or NPM1-mutant leukaemia.Menin 抑制剂 revumenib 在伴有 KMT2A 重排或 NPM1 突变的白血病中的应用。
Nature. 2023 Mar;615(7954):920-924. doi: 10.1038/s41586-023-05812-3. Epub 2023 Mar 15.
7
MEN1 mutations mediate clinical resistance to menin inhibition.MEN1 突变介导了对 menin 抑制的临床耐药性。
Nature. 2023 Mar;615(7954):913-919. doi: 10.1038/s41586-023-05755-9. Epub 2023 Mar 15.
8
Menin "reads" H3K79me2 mark in a nucleosomal context.Menin在核小体环境中“读取”H3K79me2标记。
Science. 2023 Feb 17;379(6633):717-723. doi: 10.1126/science.adc9318. Epub 2023 Feb 16.
9
Chromatin complex dependencies reveal targeting opportunities in leukemia.染色质复合物依赖性揭示白血病的靶向治疗机会。
Nat Commun. 2023 Jan 27;14(1):448. doi: 10.1038/s41467-023-36150-7.
10
Targeting Menin disrupts the KMT2A/B and polycomb balance to paradoxically activate bivalent genes.靶向 Menin 会破坏 KMT2A/B 和 polycomb 的平衡,从而反常地激活双价基因。
Nat Cell Biol. 2023 Feb;25(2):258-272. doi: 10.1038/s41556-022-01056-x. Epub 2023 Jan 12.