Xinhao Song , Yao Song , Mengjuan Lin , Moran Wang , Tianqi Jia , Juan Jin , Jingjing Sun , Genhua Duan , Xiuge Gao , Shanxiang Jiang , Feng Chen , Ning Gu , Dawei Guo
{"title":"Nano-imaging the inhibition of breast cancer cell migration by maduramicin via surface charge alteration using scanning ion conductance microscopy","authors":"Xinhao Song , Yao Song , Mengjuan Lin , Moran Wang , Tianqi Jia , Juan Jin , Jingjing Sun , Genhua Duan , Xiuge Gao , Shanxiang Jiang , Feng Chen , Ning Gu , Dawei Guo","doi":"10.1016/j.nantod.2025.102774","DOIUrl":null,"url":null,"abstract":"<div><div>Cancer cells possess a negatively charged surface that significantly influences key biological processes, including motility and invasiveness. Understanding the cellular membrane at the nanoscale level, especially in deciphering tumor migration mechanisms, is crucial yet complex. In this study, we explored the impact of maduramicin (MAD), a polyether ionophore antibiotic, on the surface charge distribution in tumor cell membranes. Our findings demonstrated that modulating calcium channels and disrupting charge distributions, imaged by a current difference-based scanning ion conductance microscopy (ΔI-SICM) method, resulted in significant reductions in both cell invasiveness and viability. These results emphasize the cell membrane's considerable role at the nano-bio interface, highlighting the intricate relationship between biophysical properties and cellular behaviors. Our research suggests that targeting the charge distribution of cell membrane may offer a novel therapeutic strategy to mitigate cell migration and enhance treatment outcomes in cancer therapy.</div></div>","PeriodicalId":395,"journal":{"name":"Nano Today","volume":"64 ","pages":"Article 102774"},"PeriodicalIF":10.9000,"publicationDate":"2025-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nano Today","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S174801322500146X","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Cancer cells possess a negatively charged surface that significantly influences key biological processes, including motility and invasiveness. Understanding the cellular membrane at the nanoscale level, especially in deciphering tumor migration mechanisms, is crucial yet complex. In this study, we explored the impact of maduramicin (MAD), a polyether ionophore antibiotic, on the surface charge distribution in tumor cell membranes. Our findings demonstrated that modulating calcium channels and disrupting charge distributions, imaged by a current difference-based scanning ion conductance microscopy (ΔI-SICM) method, resulted in significant reductions in both cell invasiveness and viability. These results emphasize the cell membrane's considerable role at the nano-bio interface, highlighting the intricate relationship between biophysical properties and cellular behaviors. Our research suggests that targeting the charge distribution of cell membrane may offer a novel therapeutic strategy to mitigate cell migration and enhance treatment outcomes in cancer therapy.
期刊介绍:
Nano Today is a journal dedicated to publishing influential and innovative work in the field of nanoscience and technology. It covers a wide range of subject areas including biomaterials, materials chemistry, materials science, chemistry, bioengineering, biochemistry, genetics and molecular biology, engineering, and nanotechnology. The journal considers articles that inform readers about the latest research, breakthroughs, and topical issues in these fields. It provides comprehensive coverage through a mixture of peer-reviewed articles, research news, and information on key developments. Nano Today is abstracted and indexed in Science Citation Index, Ei Compendex, Embase, Scopus, and INSPEC.