基于间充质干细胞靶向肿瘤微环境的高效抗癌药物递送方法:最新综述

IF 5.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY Biochemical pharmacology Pub Date : 2024-12-31 DOI:10.1016/j.bcp.2024.116725
Yang Yu, Ying Tao, Jingru Ma, Jian Li, Zhidu Song
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引用次数: 0

摘要

向癌细胞给药仍然是一项重大的治疗挑战。间充质干细胞(MSCs)具有特异性迁移到肿瘤组织的内在能力,因此很有希望成为靶向给药的候选者。临床前研究的证据表明,装载了抗癌治疗药物的间充质干细胞具有相当强的抗肿瘤活性。此外,目前有几项临床试验正在评估它们对癌症患者的疗效。间充质干细胞与合成纳米颗粒(NPs)的结合增强了它们的治疗潜力,特别是通过使用细胞膜包裹的 NPs,这代表了该领域的一大进步。本综述系统研究了肿瘤微环境、间充质干细胞的来源、肿瘤归巢机制以及间充质干细胞装载和释放抗癌药物的方法。此外,还讨论了提高基于间充质干细胞的药物递送系统(DDS)疗效的前沿策略,包括间充质干细胞膜包被纳米颗粒的创新使用。研究最后概述了间充质干细胞作为药物载体的治疗用途,包括详细分析间充质干细胞向癌细胞输送治疗药物的机制,从而实现靶向给药。研究旨在阐明这种方法的现状,确定关键的发展领域,并概述推进基于间充质干细胞的癌症疗法的潜在未来方向。
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Targeting the tumor microenvironment with mesenchymal stem cells based delivery approach for efficient delivery of anticancer agents: An updated review.

Drug delivery to cancer cells continues to present a major therapeutic challenge. Mesenchymal stem cells (MSCs) possess an intrinsic ability to migrate specifically to tumor tissues, making them promising candidates for targeted drug delivery. Evidence from preclinical studies indicates that MSCs loaded with therapeutic anti-cancer agents exhibit considerable anti-tumor activity. Moreover, several clinical trials are currently evaluating their effectiveness in cancer patients. The integration of MSCs with synthetic nanoparticles (NPs) enhances their therapeutic potential, particularly through the use of cell membrane-coated NPs, which represent a significant advancement in the field. This review systematically investigates the tumor microenvironment, the sources of MSCs, the tumor homing mechanisms, and the methods of loading and releasing anticancer drugs from MSCs. Furthermore, cutting-edge strategies to improve the efficacy of MSCs based drug delivery systems (DDS) including the innovative use of MSC membrane coated nanoparticles have been discussed. The study concludes with an overview of the therapeutic use of MSCs as drug carriers, including a detailed analysis of the mechanisms by which MSCs deliver therapeutics to cancer cells, enabling targeted drug delivery. It aims to elucidate the current state of this approach, identify key areas for development, and outline potential future directions for advancing MSCs based cancer therapies.

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来源期刊
Biochemical pharmacology
Biochemical pharmacology 医学-药学
CiteScore
10.30
自引率
1.70%
发文量
420
审稿时长
17 days
期刊介绍: Biochemical Pharmacology publishes original research findings, Commentaries and review articles related to the elucidation of cellular and tissue function(s) at the biochemical and molecular levels, the modification of cellular phenotype(s) by genetic, transcriptional/translational or drug/compound-induced modifications, as well as the pharmacodynamics and pharmacokinetics of xenobiotics and drugs, the latter including both small molecules and biologics. The journal''s target audience includes scientists engaged in the identification and study of the mechanisms of action of xenobiotics, biologics and drugs and in the drug discovery and development process. All areas of cellular biology and cellular, tissue/organ and whole animal pharmacology fall within the scope of the journal. Drug classes covered include anti-infectives, anti-inflammatory agents, chemotherapeutics, cardiovascular, endocrinological, immunological, metabolic, neurological and psychiatric drugs, as well as research on drug metabolism and kinetics. While medicinal chemistry is a topic of complimentary interest, manuscripts in this area must contain sufficient biological data to characterize pharmacologically the compounds reported. Submissions describing work focused predominately on chemical synthesis and molecular modeling will not be considered for review. While particular emphasis is placed on reporting the results of molecular and biochemical studies, research involving the use of tissue and animal models of human pathophysiology and toxicology is of interest to the extent that it helps define drug mechanisms of action, safety and efficacy.
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