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胶质母细胞瘤的治疗靶点:分子通路、新兴策略与未来方向

英文原题:Therapeutic Targets in Glioblastoma: Molecular Pathways, Emerging Strategies, and Future Directions.

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Therapeutic Targets in Glioblastoma: Molecular Pathways, Emerging Strategies, and Future Directions.

PubMed 2025/03/26(内容时间) Cells Q2 · IF 6(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

胶质母细胞瘤(GBM)是成人中侵袭性最强的原发性脑肿瘤,具有生长迅速、浸润周围脑组织及对常规治疗耐药等特点。尽管手术、放疗和化疗已有进步,中位生存期仍约为15个月,凸显了开发创新疗法的迫切需要。制定治疗方案时需考虑致癌性遗传和表观遗传改变,这些变化既可能成为治疗靶点,也可能促进治疗耐药。多种免疫治疗策略已被探索,并持续优化其抗肿瘤潜力。通过新型载体和技术(包括纳米技术)改善药物递送及穿越血脑屏障(BBB)的能力,也已取得进展。分子分型已成为个体化治疗的重要工具,可在适用时帮助确定最敏感的患者群体。本综述旨在介绍GBM潜在治疗靶点的范围,并概述关键试验结果。总体而言,必须审慎评估临床及临床前研究进展,以开发对GBM疗效最强的治疗方案。

展开英文摘要原文

Glioblastoma (GBM) is the most aggressive primary brain tumor in adults, characterized by rapid growth, invasive infiltration into surrounding brain tissue, and resistance to conventional therapies. Despite advancements in surgery, radiotherapy, and chemotherapy, median survival remains approximately 15 months, underscoring the urgent need for innovative treatments. Key considerations informing treatment development include oncogenic genetic and epigenetic alterations that may dually serve as therapeutic targets and facilitate treatment resistance. Various immunotherapeutic strategies have been explored and continue to be refined for their anti-tumor potential.

Technical aspects of drug delivery and blood-brain barrier (BBB) penetration have been addressed through novel vehicles and techniques including the incorporation of nanotechnology. Molecular profiling has emerged as an important tool to individualize treatment where applicable, and to identify patient populations with the most drug sensitivity.

The goal of this review is to describe the spectrum of potential GBM therapeutic targets, and to provide an overview of key trial outcomes. Altogether, the progress of clinical and preclinical work must be critically evaluated in order to develop therapies for GBM with the strongest therapeutic efficacy.

论文信息

作者
Tang J、Karbhari N、Campian JL
第一作者单位
Department of Biomedical Science, University of Guelph, Guelph, ON N1G 2W1, Canada.Canada
通讯作者单位
Department of Oncology, Mayo Clinic, Rochester, MN 55905, USA.United States
文献类型
综述
期刊
Cells2025 Mar 26
原文标识
PubMed 40214448 · DOI 10.3390/cells14070494