• 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

深入了解 Curaxin CBL0137 表观遗传活性的机制:诱导 DNA 去甲基化和抑制 BET 家族蛋白。

Insights into the Mechanism of Curaxin CBL0137 Epigenetic Activity: The Induction of DNA Demethylation and the Suppression of BET Family Proteins.

机构信息

Department of Chemical Carcinogenesis, Institute of Chemical Carcinogenesis, Blokhin National Medical Research Center of Oncology, 24 Kashirskoe Shosse, 115478 Moscow, Russia.

Department of Biotechnology and Industrial Pharmacy, Lomonosov Institute of Fine Chemical Technologies, Russian Technological University (MIREA), 86 Vernadsky Avenue, 119571 Moscow, Russia.

出版信息

Int J Mol Sci. 2023 Aug 17;24(16):12874. doi: 10.3390/ijms241612874.

DOI:10.3390/ijms241612874
PMID:37629054
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10454690/
Abstract

The development of malignant tumors is caused by a complex combination of genetic mutations and epigenetic alterations, the latter of which are induced by either external environmental factors or signaling disruption following genetic mutations. Some types of cancer demonstrate a significant increase in epigenetic enzymes, and targeting these epigenetic alterations represents a compelling strategy to reverse cell transcriptome to the normal state, improving chemotherapy response. Curaxin CBL0137 is a new potent anticancer drug that has been shown to activate epigenetically silenced genes. However, its detailed effects on the enzymes of the epigenetic system of transcription regulation have not been studied. Here, we report that CBL0137 inhibits the expression of DNA methyltransferase DNMT3a in HeLa TI cells, both at the level of mRNA and protein, and it decreases the level of integral DNA methylation in Ca Ski cells. For the first time, it is shown that CBL0137 decreases the level of BET family proteins, BRD2, BRD3, and BRD4, the key participants in transcription elongation, followed by the corresponding gene expression enhancement. Furthermore, we demonstrate that CBL0137 does not affect the mechanisms of histone acetylation and methylation. The ability of CBL0137 to suppress DNMT3A and BET family proteins should be taken into consideration when combined chemotherapy is applied. Our data demonstrate the potential of CBL0137 to be used in the therapy of tumors with corresponding aberrant epigenetic profiles.

摘要

肿瘤的发生是由遗传突变和表观遗传改变的复杂组合引起的,后者是由外部环境因素或遗传突变后的信号中断引起的。某些类型的癌症表现出表观遗传酶的显著增加,针对这些表观遗传改变是一种很有吸引力的策略,可以将细胞转录组逆转到正常状态,提高化疗反应。Curaxin CBL0137 是一种新的有效的抗癌药物,已被证明可以激活表观遗传沉默的基因。然而,其对转录调控的表观遗传系统酶的详细影响尚未研究。在这里,我们报告 CBL0137 抑制 HeLa TI 细胞中 DNA 甲基转移酶 DNMT3a 的表达,无论是在 mRNA 水平还是蛋白水平,并且它降低 Ca Ski 细胞中整体 DNA 甲基化水平。首次表明 CBL0137 降低了 BET 家族蛋白 BRD2、BRD3 和 BRD4 的水平,它们是转录延伸的关键参与者,随后相应基因表达增强。此外,我们证明 CBL0137 不影响组蛋白乙酰化和甲基化的机制。在联合化疗时,应考虑 CBL0137 抑制 DNMT3A 和 BET 家族蛋白的能力。我们的数据表明 CBL0137 具有用于治疗具有相应异常表观遗传谱的肿瘤的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0730/10454690/32d6e2904f31/ijms-24-12874-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0730/10454690/9590b0d89285/ijms-24-12874-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0730/10454690/40b8e1741a56/ijms-24-12874-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0730/10454690/c33557f2ae3e/ijms-24-12874-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0730/10454690/32d6e2904f31/ijms-24-12874-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0730/10454690/9590b0d89285/ijms-24-12874-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0730/10454690/40b8e1741a56/ijms-24-12874-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0730/10454690/c33557f2ae3e/ijms-24-12874-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0730/10454690/32d6e2904f31/ijms-24-12874-g004.jpg

相似文献

1
Insights into the Mechanism of Curaxin CBL0137 Epigenetic Activity: The Induction of DNA Demethylation and the Suppression of BET Family Proteins.深入了解 Curaxin CBL0137 表观遗传活性的机制:诱导 DNA 去甲基化和抑制 BET 家族蛋白。
Int J Mol Sci. 2023 Aug 17;24(16):12874. doi: 10.3390/ijms241612874.
2
Novel anticancer drug curaxin CBL0137 impairs DNA methylation by eukaryotic DNA methyltransferase Dnmt3a.新型抗癌药物 curaxin CBL0137 通过真核 DNA 甲基转移酶 Dnmt3a 损害 DNA 甲基化。
Bioorg Med Chem Lett. 2020 Aug 15;30(16):127296. doi: 10.1016/j.bmcl.2020.127296. Epub 2020 Jun 1.
3
Systematic analysis of the BET family in adrenocortical carcinoma: The expression, prognosis, gene regulation network, and regulation targets.BET 家族在肾上腺皮质癌中的系统分析:表达、预后、基因调控网络和调控靶点。
Front Endocrinol (Lausanne). 2023 Jan 30;14:1089531. doi: 10.3389/fendo.2023.1089531. eCollection 2023.
4
Effective inhibition of MYC-amplified group 3 medulloblastoma by FACT-targeted curaxin drug CBL0137.靶向 FACT 的库尔沙因药物 CBL0137 有效抑制 MYC 扩增型 3 组髓母细胞瘤。
Cell Death Dis. 2020 Dec 2;11(12):1029. doi: 10.1038/s41419-020-03201-6.
5
HeLa TI cell-based assay as a new approach to screen for chemicals able to reactivate the expression of epigenetically silenced genes.基于 HeLa TI 细胞的检测方法作为一种新的手段,用于筛选能够重新激活表观遗传沉默基因表达的化学物质。
PLoS One. 2021 Jun 11;16(6):e0252504. doi: 10.1371/journal.pone.0252504. eCollection 2021.
6
Targeting Features of Curaxin CBL0137 on Hematological Malignancies In Vitro and In Vivo.Curaxin CBL0137对血液系统恶性肿瘤的体内外靶向作用特征
Biomedicines. 2023 Jan 16;11(1):230. doi: 10.3390/biomedicines11010230.
7
Inhibition of BET Family Proteins Suppresses African Swine Fever Virus Infection.抑制BET家族蛋白可抑制非洲猪瘟病毒感染。
Microbiol Spectr. 2022 Aug 31;10(4):e0241921. doi: 10.1128/spectrum.02419-21. Epub 2022 Jun 27.
8
Targeting FAcilitates Chromatin Transcription complex inhibits pleural mesothelioma and enhances immunotherapy.靶向 FAcilitates 染色质转录复合物抑制胸膜间皮瘤并增强免疫治疗。
J Exp Clin Cancer Res. 2023 Nov 16;42(1):304. doi: 10.1186/s13046-023-02889-6.
9
Dual targeting of the epigenome via FACT complex and histone deacetylase is a potent treatment strategy for DIPG.通过 FACT 复合物和组蛋白去乙酰化酶双重靶向表观基因组是治疗弥漫性内生脑桥胶质瘤(DIPG)的有效策略。
Cell Rep. 2021 Apr 13;35(2):108994. doi: 10.1016/j.celrep.2021.108994.
10
Potent antileukemic activity of curaxin CBL0137 against MLL-rearranged leukemia.CBL0137 对 MLL 重排白血病的强效抗白血病活性。
Int J Cancer. 2020 Apr 1;146(7):1902-1916. doi: 10.1002/ijc.32582. Epub 2019 Aug 8.

本文引用的文献

1
Histone Methyltransferases as a New Target for Epigenetic Action of Vorinostat.组蛋白甲基转移酶作为伏立诺他的表观遗传作用的新靶点。
Biochemistry (Mosc). 2023 Jul;88(7):968-978. doi: 10.1134/S000629792307009X.
2
Editorial: Epigenetic drugs and therapeutic resistance for epithelial malignancies.社论:表观遗传药物与上皮性恶性肿瘤的治疗耐药性
Front Pharmacol. 2023 May 9;14:1208518. doi: 10.3389/fphar.2023.1208518. eCollection 2023.
3
Targeting Features of Curaxin CBL0137 on Hematological Malignancies In Vitro and In Vivo.Curaxin CBL0137对血液系统恶性肿瘤的体内外靶向作用特征
Biomedicines. 2023 Jan 16;11(1):230. doi: 10.3390/biomedicines11010230.
4
Mechanism of curaxin-dependent nucleosome unfolding by FACT.FACT介导的curaxin依赖性核小体解折叠机制。
Front Mol Biosci. 2022 Nov 22;9:1048117. doi: 10.3389/fmolb.2022.1048117. eCollection 2022.
5
Molecular basis of epigenetic regulation in cancer diagnosis and treatment.癌症诊断与治疗中表观遗传调控的分子基础。
Front Genet. 2022 Aug 24;13:885635. doi: 10.3389/fgene.2022.885635. eCollection 2022.
6
BRD4: a general regulator of transcription elongation.BRD4:转录延伸的通用调节剂。
Transcription. 2022 Feb-Jun;13(1-3):70-81. doi: 10.1080/21541264.2022.2108302. Epub 2022 Sep 1.
7
FACT subunit SUPT16H associates with BRD4 and contributes to silencing of interferon signaling.事实亚基 SUPT16H 与 BRD4 结合,并有助于干扰素信号的沉默。
Nucleic Acids Res. 2022 Aug 26;50(15):8700-8718. doi: 10.1093/nar/gkac645.
8
The Combination of Curaxin CBL0137 and Histone Deacetylase Inhibitor Panobinostat Delays KMT2A-Rearranged Leukemia Progression.Curaxin CBL0137与组蛋白去乙酰化酶抑制剂帕比司他联合使用可延缓KMT2A重排白血病的进展。
Front Oncol. 2022 May 23;12:863329. doi: 10.3389/fonc.2022.863329. eCollection 2022.
9
BRD2 interconnects with BRD3 to facilitate Pol II transcription initiation and elongation to prime promoters for cell differentiation.BRD2 与 BRD3 相互作用,以促进 Pol II 转录起始和延伸,为细胞分化启动启动子。
Cell Mol Life Sci. 2022 Jun 4;79(6):338. doi: 10.1007/s00018-022-04349-4.
10
Targeting Epigenetic Regulatory Enzymes for Cancer Therapeutics: Novel Small-Molecule Epidrug Development.靶向表观遗传调控酶用于癌症治疗:新型小分子表观遗传药物的开发。
Front Oncol. 2022 Mar 28;12:848221. doi: 10.3389/fonc.2022.848221. eCollection 2022.