A novel platinum(ii) complex with a berberine derivative as a potential antitumor agent targeting G-quadruplex DNA†

IF 2.7 3区 化学 Q1 CHEMISTRY, ORGANIC Organic & Biomolecular Chemistry Pub Date : 2024-12-04 DOI:10.1039/d4ob01705f
Shu-Lin Zhang , Haimei Fu , Yingxia Ma , Qifu Lin , Yanli Xu , Qiyuan Yang , Peng He , Zuzhuang Wei
{"title":"A novel platinum(ii) complex with a berberine derivative as a potential antitumor agent targeting G-quadruplex DNA†","authors":"Shu-Lin Zhang ,&nbsp;Haimei Fu ,&nbsp;Yingxia Ma ,&nbsp;Qifu Lin ,&nbsp;Yanli Xu ,&nbsp;Qiyuan Yang ,&nbsp;Peng He ,&nbsp;Zuzhuang Wei","doi":"10.1039/d4ob01705f","DOIUrl":null,"url":null,"abstract":"<div><div>G-quadruplexes are considered attractive targets for various human diseases, including cancer therapy, owing to their potential therapeutic applications. Understanding the interaction between ligands and G-quadruplexes is crucial for the development of novel anticancer agents. In this study, we designed a novel platinum(<span>ii</span>) complex (), with a berberine derivative () serving as a bioactive ligand. The structures of both ligand and were fully characterized using NMR, ESI-MS, and IR. UV-visible spectroscopy, fluorescence spectroscopy, circular dichroism spectroscopy, electrostatic surface potential, frontier molecular orbital and molecular docking experiments were employed to investigate the interaction between and G-quadruplexes. The results suggested that interacted favorably with G-quadruplex DNA over double-stranded DNA (DS26). Among them, interacts with the bcl-2 G-quadruplex with a binding affinity of 17.9 μM and did not induce conformational changes in the topology of the bcl-2 G-quadruplex. Moreover, we evaluated its antiproliferative activities on tumor cells (HeLa, A549 and T24), which demonstrated that inhibited tumor cell proliferation and induced HeLa cell apoptosis. Overall, this study offers novel insights for the development of promising platinum(<span>ii</span>) antitumor agents based on G-quadruplex structures.</div></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"23 5","pages":"Pages 1112-1119"},"PeriodicalIF":2.7000,"publicationDate":"2024-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S147705202401070X","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

Abstract

G-quadruplexes are considered attractive targets for various human diseases, including cancer therapy, owing to their potential therapeutic applications. Understanding the interaction between ligands and G-quadruplexes is crucial for the development of novel anticancer agents. In this study, we designed a novel platinum(ii) complex (), with a berberine derivative () serving as a bioactive ligand. The structures of both ligand and were fully characterized using NMR, ESI-MS, and IR. UV-visible spectroscopy, fluorescence spectroscopy, circular dichroism spectroscopy, electrostatic surface potential, frontier molecular orbital and molecular docking experiments were employed to investigate the interaction between and G-quadruplexes. The results suggested that interacted favorably with G-quadruplex DNA over double-stranded DNA (DS26). Among them, interacts with the bcl-2 G-quadruplex with a binding affinity of 17.9 μM and did not induce conformational changes in the topology of the bcl-2 G-quadruplex. Moreover, we evaluated its antiproliferative activities on tumor cells (HeLa, A549 and T24), which demonstrated that inhibited tumor cell proliferation and induced HeLa cell apoptosis. Overall, this study offers novel insights for the development of promising platinum(ii) antitumor agents based on G-quadruplex structures.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
一种新型铂(II)配合物与小檗碱衍生物作为潜在的抗肿瘤药物靶向g -四重体DNA。
由于其潜在的治疗应用,g -四联体被认为是各种人类疾病,包括癌症治疗的有吸引力的靶点。了解配体与g -四联体之间的相互作用对于开发新型抗癌药物至关重要。在这项研究中,我们设计了一种新的铂(II)配合物(Pt1),以小檗碱衍生物(L)作为生物活性配体。用NMR、ESI-MS和IR对配体L和Pt1的结构进行了全面表征。采用紫外可见光谱、荧光光谱、圆二色光谱、静电表面电位、前沿分子轨道和分子对接实验研究了Pt1与g -四联体之间的相互作用。结果表明,Pt1与g -四重体DNA的相互作用优于双链DNA (DS26)。其中,Pt1与bcl-2 g -四重体的结合亲和力为17.9 μM,未引起bcl-2 g -四重体拓扑结构的改变。此外,我们评估了Pt1对肿瘤细胞(HeLa, A549和T24)的抗增殖活性,表明Pt1抑制肿瘤细胞增殖并诱导HeLa细胞凋亡。总的来说,这项研究为开发基于g -四联结构的有前途的铂(II)抗肿瘤药物提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry 化学-有机化学
CiteScore
5.50
自引率
9.40%
发文量
1056
审稿时长
1.3 months
期刊介绍: Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.
期刊最新文献
Transaminase-triggered synthesis of 2,5-disubstituted pyrrolidines. A pre-synthetic conjugation methodology of DNA and RNA: combining on-column conjugation and tandem oligonucleotide synthesis. Ring-opening S-alkylation of sulfenamides with sulfonium salts. Adapting Bower's intramolecular aziridination reaction allows for a metal-free synthesis of N-H aziridines. Regioselective iridium(III)-catalyzed C-H cyclization using an acetylene surrogate: direct access to hydroxylated polycyclic phthalazinones.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1