Targeted therapies for glioblastoma treatment.

IF 2 4区 医学 Q3 PHYSIOLOGY Journal of Physiology and Pharmacology Pub Date : 2023-06-01 DOI:10.26402/jpp.2023.3.01
A Smolarska, I Pruszynska, W Wasylko, K Godlewska, M Markowska, A Rybak, J Botther, P Kucharzewska, J Nowakowska, J Szeliga, M Kubiak, M Gorczak, M Krol
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Abstract

Glioblastoma, the most common and aggressive type of brain tumor in adults, poses significant challenges in terms of treatment. Conventional approaches including surgery, chemotherapy, and radiotherapy have yielded limited success, with a median survival of approximately 15 months. However, extensive research into the biology of glioblastoma has identified molecular targets that can be exploited by newly developed drugs, leading to the emergence of precise personalized therapies. Several innovative treatment strategies are currently under development, aiming to enhance effectiveness while minimizing side effects. Clinical trials are underway to evaluate the efficacy of monoclonal antibodies that target glioblastoma cells, either by blocking specific receptors or by modifying molecular interactions that impede cell proliferation. Another promising avenue involves the use of oncolytic viruses designed to selectively infect glioblastoma cells. Additionally, the review explores the utilization of nanocarriers capable of surmounting the formidable obstacle of the blood-brain barrier, enabling efficient drug delivery. Cell therapies represent another promising approach, with dendritic cells, chimeric antigen receptor-T cells, and macrophages emerging as potential treatment modalities. By summarizing recent advances in targeted therapies against glioblastoma, this review aims to provide a comprehensive overview of ongoing efforts to discover effective and safe methods for treating glioblastoma patients. The ultimate goal is to improve patient outcomes and transform the landscape of glioblastoma treatment.

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胶质母细胞瘤的靶向治疗。
胶质母细胞瘤是成人中最常见和最具侵袭性的脑肿瘤,在治疗方面提出了重大挑战。包括手术、化疗和放疗在内的传统方法取得了有限的成功,中位生存期约为15个月。然而,对胶质母细胞瘤生物学的广泛研究已经确定了新开发药物可以利用的分子靶点,从而导致精确的个性化治疗的出现。目前正在开发几种创新的治疗策略,旨在提高疗效,同时尽量减少副作用。临床试验正在进行中,以评估针对胶质母细胞瘤细胞的单克隆抗体的疗效,通过阻断特定受体或通过改变阻碍细胞增殖的分子相互作用。另一个有希望的途径是使用溶瘤病毒来选择性地感染胶质母细胞瘤细胞。此外,该综述还探讨了纳米载体的利用,这些纳米载体能够克服血脑屏障的巨大障碍,从而实现有效的药物输送。细胞疗法代表了另一种有希望的方法,树突状细胞、嵌合抗原受体t细胞和巨噬细胞成为潜在的治疗方式。通过总结针对胶质母细胞瘤的靶向治疗的最新进展,本综述旨在全面概述正在进行的努力,以发现有效和安全的方法治疗胶质母细胞瘤患者。最终目标是改善患者的预后,改变胶质母细胞瘤治疗的前景。
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
4.00
自引率
22.70%
发文量
0
审稿时长
6-12 weeks
期刊介绍: Journal of Physiology and Pharmacology publishes papers which fall within the range of basic and applied physiology, pathophysiology and pharmacology. The papers should illustrate new physiological or pharmacological mechanisms at the level of the cell membrane, single cells, tissues or organs. Clinical studies, that are of fundamental importance and have a direct bearing on the pathophysiology will also be considered. Letters related to articles published in The Journal with topics of general professional interest are welcome.
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