纳米技术和热休克蛋白70在胶质母细胞瘤多形性治疗中的融合:走向精确靶向和转化的途径。

IF 2.1 Q3 PHARMACOLOGY & PHARMACY
Advances in Pharmacological and Pharmaceutical Sciences Pub Date : 2025-04-24 eCollection Date: 2025-01-01 DOI:10.1155/adpp/1847197
Amrita Arup Roy, Abhijeet Pandey, Namdev Dhas, Manasa Manjunath Hegde, Harendra S Parekh, Sai Balaji Andugulapati, Krishnadas Nandakumar, Bola Sadashiva Satish Rao, Srinivas Mutalik
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引用次数: 0

摘要

热休克蛋白70 (HSP70)和纳米技术已经成为多形性胶质母细胞瘤(GBM)治疗的有希望的途径,解决了其侵袭性和治疗耐药性带来的关键挑战。HSP70在细胞应激反应和肿瘤生存中的双重作用强调了它作为生物标志物和治疗靶点的潜力。这篇综述探讨了HSP70与纳米技术的创新整合,强调了成像、药物传递和联合治疗方面的进展。纳米粒子,包括SPIONs,脂质体,金纳米粒子和金属有机框架,通过HSP70调节显示出增强的靶向性和治疗效果。功能化纳米载体利用HSP70的肿瘤特异性过表达来改善药物传递,最小化脱靶效应并克服血脑屏障。诸如化学光疗、免疫疗法和光热疗法等新兴策略利用HSP70在肿瘤微环境中的相互作用,实现协同治疗模式。该综述还强调了转化方面的挑战,包括GBM的异质性、监管障碍和增强渗透性和滞留性(EPR)效应的可变性。整合计算模型、个性化方法和自适应试验设计对临床翻译至关重要。通过纳米技术和分子生物学的结合,hsp70靶向策略具有重新定义GBM诊断和治疗的变革潜力,为提高生存率和生活质量提供了希望。试验注册:ClinicalTrials.gov标识符:NCT00054041和NCT04628806。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Confluence of Nanotechnology and Heat Shock Protein 70 in Pioneering Glioblastoma Multiforme Therapy: Forging Pathways Towards Precision Targeting and Transformation.

Heat-shock protein 70 (HSP70) and nanotechnology have emerged as promising avenues in glioblastoma multiforme (GBM) therapy, addressing the critical challenges posed by its aggressive nature and therapeutic resistance. HSP70's dual role in cellular stress response and tumour survival emphasises its potential as both a biomarker and therapeutic target. This review explores the innovative integration of HSP70 with nanotechnology, emphasising advancements in imaging, drug delivery and combination therapies. Nanoparticles, including SPIONs, liposomes, gold nanoparticles and metal-organic frameworks, demonstrate enhanced targeting and therapeutic efficacy through HSP70 modulation. Functionalized nanocarriers exploit HSP70's tumour-specific overexpression to improve drug delivery, minimise off-target effects and overcome the blood-brain barrier. Emerging strategies such as chemophototherapy, immunotherapy and photothermal therapy leverage HSP70's interactions within the tumour microenvironment, enabling synergistic treatment modalities. The review also highlights translational challenges, including heterogeneity of GBM, regulatory hurdles and variability in the enhanced permeability and retention (EPR) effect. Integrating computational modelling, personalised approaches and adaptive trial designs is crucial for clinical translation. By bridging nanotechnology and molecular biology, HSP70-targeted strategies hold transformative potential to redefine GBM diagnosis and treatment, offering hope for improved survival and quality of life. Trial Registration: ClinicalTrials.gov identifier: NCT00054041 and NCT04628806.

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CiteScore
4.30
自引率
3.60%
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审稿时长
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