Precision Nanomedicine for Cancer: Innovations, Strategies, and Translational Challenges.

IF 2.8 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
OncoTargets and therapy Pub Date : 2025-10-10 eCollection Date: 2025-01-01 DOI:10.2147/OTT.S550104
Fuxing Wen, Lishuang Wang, Xian Li, Jiajia Zhao, Tingting Xu, Jingkai Zhu, Lijuan Ma, Xiaodong Wang
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Abstract

As nanotechnology advances rapidly, it has propelled nanomedicine into a revolutionary frontier for anticancer therapy. This review comprehensively analyzes the core principles, key innovations, and strategic approaches driving the development of targeted nanotherapeutics against tumors. We elucidate the distinctive properties of nanoscale drug delivery systems (eg, liposomes, polymeric nanoparticles, inorganic nanoparticles, and hybrid systems) and their capacity to be designed to surmount the constraints of traditional cancer treatments by potentially augmenting drug specificity, bioavailability, and minimizing systemic toxicity, with some nanocarriers (eg, liposomal doxorubicin) already approved for clinical use. With a focus on both the enhanced permeability and retention (EPR) effect-mediated passive targeting and ligand-based active targeting mechanisms employing peptides, aptamers, and antibodies, we investigate how these nanocarriers are engineered for efficient tumor-targeted drug delivery. The review further delves into the understanding of nano-bio interactions (eg, size-dependent cellular uptake) and their interplay with cancer biology. We discuss how this knowledge, alongside the rational design of stimuli-responsive and multifunctional "smart" nanoplatforms, informs the development of more precise and effective therapeutic strategies. Finally, we address the ongoing challenges in clinical translation, such as patient heterogeneity and physiological barriers, and emphasize that comprehending these aspects is pivotal for guiding future translational research towards the realization of truly patient-centric nanomedicines.

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癌症的精密纳米医学:创新、策略和转化挑战。
随着纳米技术的迅速发展,它已经推动纳米医学进入抗癌治疗的革命性前沿。本文全面分析了推动肿瘤靶向纳米治疗发展的核心原则、关键创新和战略途径。我们阐明了纳米级药物递送系统(如脂质体、聚合纳米颗粒、无机纳米颗粒和混合系统)的独特特性,以及它们通过潜在地增强药物特异性、生物利用度和最小化全身毒性来克服传统癌症治疗限制的能力,一些纳米载体(如脂质体阿霉素)已经被批准用于临床使用。重点关注增强渗透性和滞留性(EPR)效应介导的被动靶向和基于配体的主动靶向机制,利用肽、适体和抗体,我们研究了这些纳米载体如何被设计为有效的肿瘤靶向药物递送。这篇综述进一步深入研究了纳米生物相互作用(例如,大小依赖的细胞摄取)及其与癌症生物学的相互作用。我们讨论了这些知识,以及刺激反应和多功能“智能”纳米平台的合理设计,如何为更精确和有效的治疗策略的发展提供信息。最后,我们讨论了临床翻译中存在的挑战,如患者异质性和生理障碍,并强调理解这些方面对于指导未来的转化研究,实现真正以患者为中心的纳米药物至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
OncoTargets and therapy
OncoTargets and therapy BIOTECHNOLOGY & APPLIED MICROBIOLOGY-ONCOLOGY
CiteScore
9.70
自引率
0.00%
发文量
221
审稿时长
1 months
期刊介绍: OncoTargets and Therapy is an international, peer-reviewed journal focusing on molecular aspects of cancer research, that is, the molecular diagnosis of and targeted molecular or precision therapy for all types of cancer. The journal is characterized by the rapid reporting of high-quality original research, basic science, reviews and evaluations, expert opinion and commentary that shed novel insight on a cancer or cancer subtype. Specific topics covered by the journal include: -Novel therapeutic targets and innovative agents -Novel therapeutic regimens for improved benefit and/or decreased side effects -Early stage clinical trials Further considerations when submitting to OncoTargets and Therapy: -Studies containing in vivo animal model data will be considered favorably. -Tissue microarray analyses will not be considered except in cases where they are supported by comprehensive biological studies involving multiple cell lines. -Biomarker association studies will be considered only when validated by comprehensive in vitro data and analysis of human tissue samples. -Studies utilizing publicly available data (e.g. GWAS/TCGA/GEO etc.) should add to the body of knowledge about a specific disease or relevant phenotype and must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Bioinformatics studies must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Single nucleotide polymorphism (SNP) studies will not be considered.
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