• 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

具有重大影响的小分子:Metarrestin靶向癌症转移中的核仁周围区室。

Small Molecule with Big Impact: Metarrestin Targets the Perinucleolar Compartment in Cancer Metastasis.

作者信息

Kashyap Vivek K, Sharma Bhuvnesh P, Pandey Divya, Singh Ajay K, Peasah-Darkwah Godwin, Singh Bhupesh, Roy Kuldeep K, Yallapu Murali M, Chauhan Subhash C

机构信息

Division of Cancer Immunology and Microbiology, Medicine, and Oncology Integrated Service Unit, School of Medicine, University of Texas Rio Grande Valley, McAllen, TX 78504, USA.

South Texas Center of Excellence in Cancer Research (ST-CECR), McAllen, TX 78504, USA.

出版信息

Cells. 2024 Dec 12;13(24):2053. doi: 10.3390/cells13242053.

DOI:10.3390/cells13242053
PMID:39768145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11674295/
Abstract

Metarrestin (ML246) is a first-in-class pyrrole-pyrimidine-derived small molecule that selectively targets the perinucleolar compartment (PNC). PNC is a distinct subnuclear structure predominantly found in solid tumor cells. The occurrence of PNC demonstrates a positive correlation with malignancy, serving as an indicator of tumor aggressiveness, progression, and metastasis. Various promising preclinical results have led to the clinical translation of metarrestin into a first-in-human trial. This review aims to summarize (i) the current understanding of the structure and function of PNC and its role in cancer progression and metastasis, (ii) key findings from studies examining the effect of metarrestin on various cancers across the translational spectrum, including in vitro, in vivo, and human clinical trial studies, and (iii) the pharmaceutical relevance of metarrestin as a promising anticancer candidate. Furthermore, our molecular docking and MD simulation studies show that metarrestin binds to eEF1A1 and eEF1A2 with a strong and stable affinity and inhibits eEF1A2 more efficiently compared to eEF1A1. The promising results from preclinical studies suggest that metarrestin has the potential to revolutionize the treatment of cancer, heralding a paradigm shift in its therapeutic management.

摘要

美他瑞司汀(ML246)是一种新型的源自吡咯 - 嘧啶的小分子,它选择性地靶向核仁周区(PNC)。PNC是一种独特的亚核结构,主要存在于实体瘤细胞中。PNC的出现与恶性肿瘤呈正相关,可作为肿瘤侵袭性、进展和转移的指标。各种有前景的临床前研究结果已促使美他瑞司汀进入首次人体试验的临床转化阶段。本综述旨在总结:(i)目前对PNC的结构和功能及其在癌症进展和转移中的作用的理解;(ii)研究美他瑞司汀对跨转化谱的各种癌症的影响的研究的关键发现,包括体外、体内和人体临床试验研究;(iii)美他瑞司汀作为一种有前景的抗癌候选药物的药学相关性。此外,我们的分子对接和分子动力学模拟研究表明,美他瑞司汀以强而稳定的亲和力与eEF1A1和eEF1A2结合,并且与eEF1A1相比,能更有效地抑制eEF1A2。临床前研究的有前景结果表明,美他瑞司汀有可能彻底改变癌症治疗方式,预示着其治疗管理的范式转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b841/11674295/dd9096c2bdda/cells-13-02053-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b841/11674295/b04c2f4d7e6e/cells-13-02053-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b841/11674295/d4c5d4c9f101/cells-13-02053-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b841/11674295/bf6ef629c06c/cells-13-02053-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b841/11674295/f64e07dd3769/cells-13-02053-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b841/11674295/dd9096c2bdda/cells-13-02053-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b841/11674295/b04c2f4d7e6e/cells-13-02053-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b841/11674295/d4c5d4c9f101/cells-13-02053-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b841/11674295/bf6ef629c06c/cells-13-02053-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b841/11674295/f64e07dd3769/cells-13-02053-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b841/11674295/dd9096c2bdda/cells-13-02053-g005.jpg

相似文献

1
Small Molecule with Big Impact: Metarrestin Targets the Perinucleolar Compartment in Cancer Metastasis.具有重大影响的小分子:Metarrestin靶向癌症转移中的核仁周围区室。
Cells. 2024 Dec 12;13(24):2053. doi: 10.3390/cells13242053.
2
Pharmacokinetic evaluation of the PNC disassembler metarrestin in wild-type and Pdx1-Cre;LSL-Kras;Tp53 (KPC) mice, a genetically engineered model of pancreatic cancer.PNC 解聚酶美替拉嗪在野生型和 Pdx1-Cre;LSL-Kras;Tp53(KPC)小鼠中的药代动力学评价,一种胰腺癌的基因工程模型。
Cancer Chemother Pharmacol. 2018 Dec;82(6):1067-1080. doi: 10.1007/s00280-018-3699-0. Epub 2018 Oct 10.
3
Metarrestin, a perinucleolar compartment inhibitor, effectively suppresses metastasis.核仁周腔抑制剂 Metarrestin 可有效抑制转移。
Sci Transl Med. 2018 May 16;10(441). doi: 10.1126/scitranslmed.aap8307.
4
Discovery and Optimization of Pyrrolopyrimidine Derivatives as Selective Disruptors of the Perinucleolar Compartment, a Marker of Tumor Progression toward Metastasis.发现并优化吡咯嘧啶衍生物作为核周腔的选择性破坏剂,核周腔是肿瘤转移进展的标志物。
J Med Chem. 2022 Jun 23;65(12):8303-8331. doi: 10.1021/acs.jmedchem.2c00204. Epub 2022 Jun 13.
5
Safety assessment of metarrestin in dogs: A clinical candidate targeting a subnuclear structure unique to metastatic cancer cells.美他雷司汀在犬类中的安全性评估:一种针对转移性癌细胞特有亚核结构的临床候选药物。
Regul Toxicol Pharmacol. 2020 Oct;116:104716. doi: 10.1016/j.yrtph.2020.104716. Epub 2020 Jun 30.
6
Determination of metarrestin (ML-246) in human plasma for a first-in-human clinical pharmacokinetic application by a simple and efficient uHPLC-MS/MS assay.采用简单高效的 UHPLC-MS/MS 法测定人血浆中的美替拉酮(ML-246),用于首次人体临床药代动力学研究。
J Chromatogr B Analyt Technol Biomed Life Sci. 2023 May 30;1224:123738. doi: 10.1016/j.jchromb.2023.123738. Epub 2023 May 6.
7
Metabolism and pharmacokinetics characterization of metarrestin in multiple species.在多种物种中对美他雷司汀的代谢和药代动力学特征进行研究。
Cancer Chemother Pharmacol. 2020 Apr;85(4):805-816. doi: 10.1007/s00280-020-04042-y. Epub 2020 Mar 17.
8
The perinucleolar compartment.核仁周隙。
Cold Spring Harb Perspect Biol. 2010 Feb;2(2):a000679. doi: 10.1101/cshperspect.a000679.
9
The perinucleolar compartment: structure, function, and utility in anti-cancer drug development.核仁周围区室:结构、功能及其在抗癌药物研发中的应用
Nucleus. 2024 Dec;15(1):2306777. doi: 10.1080/19491034.2024.2306777. Epub 2024 Jan 27.
10
A small molecule inhibitor of the perinucleolar compartment, ML246, attenuates growth and spread of ovarian cancer.一种核仁周围区室的小分子抑制剂ML246可减弱卵巢癌的生长和扩散。
Gynecol Oncol Res Pract. 2018 Oct 2;5:7. doi: 10.1186/s40661-018-0064-2. eCollection 2018.

引用本文的文献

1
Targeting Eukaryotic Elongation Factor 1A: How Small-Molecule Inhibitors Suppress Tumor Growth via Diverse Pathways.靶向真核生物延伸因子1A:小分子抑制剂如何通过多种途径抑制肿瘤生长。
Int J Mol Sci. 2025 Jul 29;26(15):7331. doi: 10.3390/ijms26157331.

本文引用的文献

1
Curcumin attenuates smoking and drinking activated NF-κB/IL-6 inflammatory signaling axis in cervical cancer.姜黄素可减轻吸烟和饮酒激活的宫颈癌中的NF-κB/IL-6炎症信号轴。
Cancer Cell Int. 2024 Oct 20;24(1):343. doi: 10.1186/s12935-024-03513-z.
2
Mechanism insights and therapeutic intervention of tumor metastasis: latest developments and perspectives.肿瘤转移的机制洞察与治疗干预:最新进展与展望
Signal Transduct Target Ther. 2024 Aug 2;9(1):192. doi: 10.1038/s41392-024-01885-2.
3
Exploring treatment options in cancer: Tumor treatment strategies.
探索癌症的治疗选择:肿瘤治疗策略。
Signal Transduct Target Ther. 2024 Jul 17;9(1):175. doi: 10.1038/s41392-024-01856-7.
4
Conquering chemoresistance in pancreatic cancer: Exploring novel drug therapies and delivery approaches amidst desmoplasia and hypoxia.攻克胰腺癌的化疗耐药性:在间质纤维化和缺氧环境中探索新的药物治疗和递药方法。
Cancer Lett. 2024 Apr 28;588:216782. doi: 10.1016/j.canlet.2024.216782. Epub 2024 Mar 6.
5
The perinucleolar compartment: structure, function, and utility in anti-cancer drug development.核仁周围区室:结构、功能及其在抗癌药物研发中的应用
Nucleus. 2024 Dec;15(1):2306777. doi: 10.1080/19491034.2024.2306777. Epub 2024 Jan 27.
6
Cancer statistics, 2024.2024年癌症统计数据。
CA Cancer J Clin. 2024 Jan-Feb;74(1):12-49. doi: 10.3322/caac.21820. Epub 2024 Jan 17.
7
Oncogenic activation of EEF1A2 expression: a journey from a putative to an established oncogene.EEF1A2 表达的致癌激活:从假定癌基因到确立的癌基因之旅。
Cell Mol Biol Lett. 2024 Jan 3;29(1):6. doi: 10.1186/s11658-023-00519-9.
8
The Bioavailability of Drugs-The Current State of Knowledge.药物的生物利用度——当前的知识状况。
Molecules. 2023 Dec 11;28(24):8038. doi: 10.3390/molecules28248038.
9
Targeting the RAS/RAF/MAPK pathway for cancer therapy: from mechanism to clinical studies.靶向 RAS/RAF/MAPK 通路治疗癌症:从机制到临床研究。
Signal Transduct Target Ther. 2023 Dec 18;8(1):455. doi: 10.1038/s41392-023-01705-z.
10
Dual role of Snail1 as transcriptional repressor and activator.Snail1 的双重转录抑制子和激活子功能。
Biochim Biophys Acta Rev Cancer. 2024 Jan;1879(1):189037. doi: 10.1016/j.bbcan.2023.189037. Epub 2023 Dec 2.