Efficient on-demand cuproptosis induction against triple-negative breast cancer via dual-responsive black phosphorus nanosheet

IF 8.7 1区 医学 Q1 ENGINEERING, BIOMEDICAL
Qiancun Hong , Jiajun Huang , Zhiguo Li , Yue Chen , Jiawei Wang , Tongrui Shang , Zelin Chen , Cong Luo , Yongqiang Wang , Xinghong Tang , Taojian Fan , Songyin Huang , Hao Fu , Yandan Yao
{"title":"Efficient on-demand cuproptosis induction against triple-negative breast cancer via dual-responsive black phosphorus nanosheet","authors":"Qiancun Hong ,&nbsp;Jiajun Huang ,&nbsp;Zhiguo Li ,&nbsp;Yue Chen ,&nbsp;Jiawei Wang ,&nbsp;Tongrui Shang ,&nbsp;Zelin Chen ,&nbsp;Cong Luo ,&nbsp;Yongqiang Wang ,&nbsp;Xinghong Tang ,&nbsp;Taojian Fan ,&nbsp;Songyin Huang ,&nbsp;Hao Fu ,&nbsp;Yandan Yao","doi":"10.1016/j.mtbio.2025.101985","DOIUrl":null,"url":null,"abstract":"<div><div>Cuproptosis, a newly identified cell death pathway, has been shown by our analyses to be closely associated with the clinical prognosis of triple-negative breast cancer (TNBC) patients and may potentially facilitate the elimination of TNBC. However, precisely and efficiently regulating cuproptosis in tumor regions in a controllable manner remains challenging. Here, a highly effective cuproptosis inducer based on black phosphorus nanosheets (BPNs@Cu@PDA, denoted as BCP) is constructed, featuring acidic and thermal-responsive copper ion release, as well as enhanced cuprous ion (Cu<sup>+</sup>) loading capability. Briefly, BCP efficiently increases the loading proportion of Cu<sup>+</sup> via inherent surface redox reactions between phosphorus and copper ions (Cu<sup>2+</sup>), thereby enabling a significantly elevated cuproptosis induction ability. After accumulating at the tumor, BCP precisely releases Cu<sup>+/2+</sup> in response to the photo-hyperthermia and acidic microenvironment created by the dopamine modification, thereby efficiently producing reactive hydroxyl radicals (•OH) through Cu<sup>+/2+</sup>-dependent Fenton-like reactions, which leads to significant oxidative damage in TNBC cells. The precisely released Cu<sup>+/2+</sup> further inhibits the production of the Fe-S cluster while causing the aggregation of succinylated proteins, leading to significantly disrupted mitochondrial function and the TCA cycle, thereby inducing significant cuproptosis and subsequent TNBC suppression (over 90 % decrease in tumor volumes) in a synergistic manner. This research presents a novel cuproptosis induction strategy specifically designed for TNBC that has negligible toxicity, which may provide insights into the clinical treatment of TNBC.</div></div>","PeriodicalId":18310,"journal":{"name":"Materials Today Bio","volume":"33 ","pages":"Article 101985"},"PeriodicalIF":8.7000,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Today Bio","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590006425005551","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Cuproptosis, a newly identified cell death pathway, has been shown by our analyses to be closely associated with the clinical prognosis of triple-negative breast cancer (TNBC) patients and may potentially facilitate the elimination of TNBC. However, precisely and efficiently regulating cuproptosis in tumor regions in a controllable manner remains challenging. Here, a highly effective cuproptosis inducer based on black phosphorus nanosheets (BPNs@Cu@PDA, denoted as BCP) is constructed, featuring acidic and thermal-responsive copper ion release, as well as enhanced cuprous ion (Cu+) loading capability. Briefly, BCP efficiently increases the loading proportion of Cu+ via inherent surface redox reactions between phosphorus and copper ions (Cu2+), thereby enabling a significantly elevated cuproptosis induction ability. After accumulating at the tumor, BCP precisely releases Cu+/2+ in response to the photo-hyperthermia and acidic microenvironment created by the dopamine modification, thereby efficiently producing reactive hydroxyl radicals (•OH) through Cu+/2+-dependent Fenton-like reactions, which leads to significant oxidative damage in TNBC cells. The precisely released Cu+/2+ further inhibits the production of the Fe-S cluster while causing the aggregation of succinylated proteins, leading to significantly disrupted mitochondrial function and the TCA cycle, thereby inducing significant cuproptosis and subsequent TNBC suppression (over 90 % decrease in tumor volumes) in a synergistic manner. This research presents a novel cuproptosis induction strategy specifically designed for TNBC that has negligible toxicity, which may provide insights into the clinical treatment of TNBC.
双响应黑磷纳米片对三阴性乳腺癌有效的按需铜诱导作用
cuprotosis是一种新发现的细胞死亡途径,我们的分析表明,它与三阴性乳腺癌(TNBC)患者的临床预后密切相关,并可能促进TNBC的消除。然而,以可控的方式精确有效地调节肿瘤区域的铜突仍然是一个挑战。本文构建了一种基于黑磷纳米片(BPNs@Cu@PDA,表示为BCP)的高效铜还原诱导剂,具有酸性和热响应性铜离子释放,以及增强的铜离子(Cu+)加载能力。简而言之,BCP通过磷与铜离子(Cu2+)之间固有的表面氧化还原反应有效地增加了Cu+的负载比例,从而显著提高了铜还原诱导能力。BCP在肿瘤中积累后,在多巴胺修饰产生的光热和酸性微环境下精确释放Cu+/2+,从而通过Cu+/2+依赖的芬顿样反应有效产生活性羟基自由基(•OH),导致TNBC细胞明显的氧化损伤。精确释放的Cu+/2+进一步抑制Fe-S簇的产生,同时引起琥珀酰化蛋白的聚集,导致线粒体功能和TCA循环明显中断,从而以协同方式诱导显著的铜增生和随后的TNBC抑制(肿瘤体积减少90%以上)。本研究提出了一种专为TNBC设计的新型铜增生诱导策略,其毒性可忽略不计,这可能为TNBC的临床治疗提供见解。
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 求助全文
来源期刊
CiteScore
8.30
自引率
4.90%
发文量
303
审稿时长
30 days
期刊介绍: Materials Today Bio is a multidisciplinary journal that specializes in the intersection between biology and materials science, chemistry, physics, engineering, and medicine. It covers various aspects such as the design and assembly of new structures, their interaction with biological systems, functionalization, bioimaging, therapies, and diagnostics in healthcare. The journal aims to showcase the most significant advancements and discoveries in this field. As part of the Materials Today family, Materials Today Bio provides rigorous peer review, quick decision-making, and high visibility for authors. It is indexed in Scopus, PubMed Central, Emerging Sources, Citation Index (ESCI), and Directory of Open Access Journals (DOAJ).
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信