基于单细胞的癌症研究的先进微流体。

IF 14.1 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Adriana Carneiro, Marta Aranda Palomer, Margarida Esteves, Carolina Rodrigues, José Maria Fernandes, Francisca Oliveira, Alexandra Teixeira, Carlos Honrado, Lorena Dieguez, Sara Abalde-Cela, Miguel Xavier
{"title":"基于单细胞的癌症研究的先进微流体。","authors":"Adriana Carneiro, Marta Aranda Palomer, Margarida Esteves, Carolina Rodrigues, José Maria Fernandes, Francisca Oliveira, Alexandra Teixeira, Carlos Honrado, Lorena Dieguez, Sara Abalde-Cela, Miguel Xavier","doi":"10.1002/advs.202500975","DOIUrl":null,"url":null,"abstract":"<p><p>Cancer remains one of the leading causes of mortality worldwide, accounting for ≈10 million deaths annually. Critically, it is metastasis and not the primary tumour that causes most of these deaths. Understanding the mechanisms behind cancer dissemination and therapy resistance is thus a pressing challenge. Traditional bulk tissue analyses have failed to capture the full spectrum of intra-tumour heterogeneity and the dynamic interactions within the tumour microenvironment. Studying cancer at the single-cell level allows unravelling the roles of rare subpopulations, cell-cell interactions, and spatial dynamics that govern tumour evolution, metastasis, and immune evasion. This review explores how recent advances in microfluidic technologies are transforming ability to model and study cancer at the single-cell level. Cutting-edge platforms are highlighted, including droplet microfluidics, single cell-derived spheroids, and tumour-chips, that enable physiologically relevant 3D cancer models. By integrating immune components, biosensing, and patient-derived materials, these platforms hold promise for advancing drug screening, immunotherapy assessment, and personalised medicine. It is concluded by identifying key challenges and priorities for future work, which should focus on increasing model complexity, reproducibility, and integration of spatiotemporal multiomics to better dissect tumour heterogeneity and accelerate clinical translation.</p>","PeriodicalId":117,"journal":{"name":"Advanced Science","volume":" ","pages":"e00975"},"PeriodicalIF":14.1000,"publicationDate":"2025-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Advanced Microfluidics for Single Cell-Based Cancer Research.\",\"authors\":\"Adriana Carneiro, Marta Aranda Palomer, Margarida Esteves, Carolina Rodrigues, José Maria Fernandes, Francisca Oliveira, Alexandra Teixeira, Carlos Honrado, Lorena Dieguez, Sara Abalde-Cela, Miguel Xavier\",\"doi\":\"10.1002/advs.202500975\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Cancer remains one of the leading causes of mortality worldwide, accounting for ≈10 million deaths annually. Critically, it is metastasis and not the primary tumour that causes most of these deaths. Understanding the mechanisms behind cancer dissemination and therapy resistance is thus a pressing challenge. Traditional bulk tissue analyses have failed to capture the full spectrum of intra-tumour heterogeneity and the dynamic interactions within the tumour microenvironment. Studying cancer at the single-cell level allows unravelling the roles of rare subpopulations, cell-cell interactions, and spatial dynamics that govern tumour evolution, metastasis, and immune evasion. This review explores how recent advances in microfluidic technologies are transforming ability to model and study cancer at the single-cell level. Cutting-edge platforms are highlighted, including droplet microfluidics, single cell-derived spheroids, and tumour-chips, that enable physiologically relevant 3D cancer models. By integrating immune components, biosensing, and patient-derived materials, these platforms hold promise for advancing drug screening, immunotherapy assessment, and personalised medicine. It is concluded by identifying key challenges and priorities for future work, which should focus on increasing model complexity, reproducibility, and integration of spatiotemporal multiomics to better dissect tumour heterogeneity and accelerate clinical translation.</p>\",\"PeriodicalId\":117,\"journal\":{\"name\":\"Advanced Science\",\"volume\":\" \",\"pages\":\"e00975\"},\"PeriodicalIF\":14.1000,\"publicationDate\":\"2025-07-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Science\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/advs.202500975\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Science","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/advs.202500975","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

摘要

癌症仍然是全世界死亡的主要原因之一,每年约有1 000万人死亡。关键的是,大多数死亡是由肿瘤转移而非原发肿瘤引起的。因此,了解癌症传播和治疗耐药性背后的机制是一项紧迫的挑战。传统的大块组织分析未能捕获肿瘤内异质性的全谱和肿瘤微环境内的动态相互作用。在单细胞水平上研究癌症可以揭示罕见亚群、细胞-细胞相互作用和控制肿瘤进化、转移和免疫逃避的空间动力学的作用。这篇综述探讨了微流体技术的最新进展如何在单细胞水平上改变癌症模型和研究的能力。重点介绍了尖端平台,包括液滴微流体,单细胞衍生球体和肿瘤芯片,这些平台可以实现生理学相关的3D癌症模型。通过整合免疫成分、生物传感和患者来源的材料,这些平台有望推进药物筛选、免疫治疗评估和个性化医疗。最后,我们确定了未来工作的关键挑战和重点,这些工作应侧重于提高模型的复杂性、可重复性和时空多组学的整合,以更好地解剖肿瘤异质性并加速临床转化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advanced Microfluidics for Single Cell-Based Cancer Research.

Cancer remains one of the leading causes of mortality worldwide, accounting for ≈10 million deaths annually. Critically, it is metastasis and not the primary tumour that causes most of these deaths. Understanding the mechanisms behind cancer dissemination and therapy resistance is thus a pressing challenge. Traditional bulk tissue analyses have failed to capture the full spectrum of intra-tumour heterogeneity and the dynamic interactions within the tumour microenvironment. Studying cancer at the single-cell level allows unravelling the roles of rare subpopulations, cell-cell interactions, and spatial dynamics that govern tumour evolution, metastasis, and immune evasion. This review explores how recent advances in microfluidic technologies are transforming ability to model and study cancer at the single-cell level. Cutting-edge platforms are highlighted, including droplet microfluidics, single cell-derived spheroids, and tumour-chips, that enable physiologically relevant 3D cancer models. By integrating immune components, biosensing, and patient-derived materials, these platforms hold promise for advancing drug screening, immunotherapy assessment, and personalised medicine. It is concluded by identifying key challenges and priorities for future work, which should focus on increasing model complexity, reproducibility, and integration of spatiotemporal multiomics to better dissect tumour heterogeneity and accelerate clinical translation.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Advanced Science
Advanced Science CHEMISTRY, MULTIDISCIPLINARYNANOSCIENCE &-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
18.90
自引率
2.60%
发文量
1602
审稿时长
1.9 months
期刊介绍: Advanced Science is a prestigious open access journal that focuses on interdisciplinary research in materials science, physics, chemistry, medical and life sciences, and engineering. The journal aims to promote cutting-edge research by employing a rigorous and impartial review process. It is committed to presenting research articles with the highest quality production standards, ensuring maximum accessibility of top scientific findings. With its vibrant and innovative publication platform, Advanced Science seeks to revolutionize the dissemination and organization of scientific knowledge.
×
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