Targeting prostate tumour and its stroma by nanoparticles.

IF 3.9 4区 医学 Q1 PHARMACOLOGY & PHARMACY
Dongliang Liao, Tian Pu, Peng Tian
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引用次数: 0

Abstract

The stroma plays a pivotal role in the development of prostate tumours. The tumour stroma includes different immune and stromal cells. Stromal cells can include fibroblasts, activated fibroblasts, endothelial cells, stem cells, etc. Immune system cells also consist of different subsets of T cells, B cells, macrophages and myeloid cells. Targeting different cells and their expressed or released molecules and genes in the tumour stroma has been proposed as an intriguing strategy for remodelling stroma and repressing prostate cancer (PCa) growth. Leveraging nanotechnology, researchers have developed innovative strategies to target these components. This review examines the latest progress in nanoparticle-based therapies specifically designed to interact with the prostate tumour stroma. We overview the functionalisation and targeting mechanisms of various nanoparticles, including organic and inorganic nanoparticles, highlighting their ability to specifically target stromal elements such as fibroblasts, extracellular matrix (ECM) and immune cells in PCa. Furthermore, we evaluate the synergistic potential of combining nanoparticle-based targeting with other therapies such as chemotherapy, radiotherapy, targeted therapy and photothermal and photodynamic therapies.

利用纳米颗粒靶向前列腺肿瘤及其基质。
基质在前列腺肿瘤的发展中起着关键作用。肿瘤基质包括不同的免疫细胞和基质细胞。基质细胞包括成纤维细胞、活化成纤维细胞、内皮细胞、干细胞等。免疫系统细胞还包括T细胞、B细胞、巨噬细胞和骨髓细胞的不同亚群。靶向肿瘤基质中的不同细胞及其表达或释放的分子和基因已被提出作为一种重塑基质和抑制前列腺癌(PCa)生长的有趣策略。利用纳米技术,研究人员开发了针对这些成分的创新策略。本文综述了纳米颗粒治疗前列腺肿瘤基质的最新进展。我们概述了各种纳米颗粒的功能化和靶向机制,包括有机纳米颗粒和无机纳米颗粒,强调了它们特异性靶向PCa中的基质元素(如成纤维细胞、细胞外基质(ECM)和免疫细胞)的能力。此外,我们还评估了纳米颗粒靶向与其他疗法(如化疗、放疗、靶向治疗、光热和光动力疗法)结合的协同潜力。
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
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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