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Targeted Arginine Metabolism Therapy: A Dilemma in Glioma Treatment.靶向精氨酸代谢疗法:胶质瘤治疗中的一个困境
Front Oncol. 2022 Jul 11;12:938847. doi: 10.3389/fonc.2022.938847. eCollection 2022.
2
Polymeric Nanoparticles in Brain Cancer Therapy: A Review of Current Approaches.用于脑癌治疗的聚合物纳米颗粒:当前方法综述
Polymers (Basel). 2022 Jul 21;14(14):2963. doi: 10.3390/polym14142963.
3
Efficacy of Cytokine-Induced Killer Cell Immunotherapy for Patients With Pathologically Pure Glioblastoma.细胞因子诱导的杀伤细胞免疫疗法对病理纯型胶质母细胞瘤患者的疗效
Front Oncol. 2022 Apr 8;12:851628. doi: 10.3389/fonc.2022.851628. eCollection 2022.
4
A phase 1 study of IDH305 in patients with IDH1-mutant acute myeloid leukemia or myelodysplastic syndrome.IDH305用于IDH1突变型急性髓系白血病或骨髓增生异常综合征患者的1期研究。
J Cancer Res Clin Oncol. 2023 Mar;149(3):1145-1158. doi: 10.1007/s00432-022-03983-6. Epub 2022 Mar 30.
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Cancer vaccines as promising immuno-therapeutics: platforms and current progress.癌症疫苗作为有前途的免疫疗法:平台和当前进展。
J Hematol Oncol. 2022 Mar 18;15(1):28. doi: 10.1186/s13045-022-01247-x.
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Delivering Therapeutics to Glioblastoma: Overcoming Biological Constraints.将治疗药物递送至脑胶质瘤:克服生物学限制。
Int J Mol Sci. 2022 Feb 2;23(3):1711. doi: 10.3390/ijms23031711.
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Glioma targeted therapy: insight into future of molecular approaches.脑胶质瘤靶向治疗:分子靶向治疗的未来展望。
Mol Cancer. 2022 Feb 8;21(1):39. doi: 10.1186/s12943-022-01513-z.
8
Immunotherapy for glioblastoma: the promise of combination strategies.胶质母细胞瘤的免疫治疗:联合策略的前景。
J Exp Clin Cancer Res. 2022 Jan 25;41(1):35. doi: 10.1186/s13046-022-02251-2.
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Grand Challenges in Nano-Based Drug Delivery.基于纳米技术的药物递送面临的重大挑战。
Front Med Technol. 2019 Dec 3;1:1. doi: 10.3389/fmedt.2019.00001. eCollection 2019.
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In Vitro and Clinical Compassionate Use Experiences with the Drug-Repurposing Approach CUSP9v3 in Glioblastoma.胶质母细胞瘤中药物重新利用方法CUSP9v3的体外及临床同情用药经验
Pharmaceuticals (Basel). 2021 Nov 29;14(12):1241. doi: 10.3390/ph14121241.

分子靶向治疗:胶质母细胞瘤治疗的新途径。

Molecular targeted therapy: A new avenue in glioblastoma treatment.

作者信息

El Atat Oula, Naser Rayan, Abdelkhalek Maya, Habib Ralph Abi, El Sibai Mirvat

机构信息

Department of Natural Sciences, School of Arts and Sciences, Lebanese American University, Beirut 1102 2801, Lebanon.

出版信息

Oncol Lett. 2022 Dec 15;25(2):46. doi: 10.3892/ol.2022.13632. eCollection 2023 Feb.

DOI:10.3892/ol.2022.13632
PMID:36644133
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9811647/
Abstract

Glioblastoma, also referred to as glioblastoma multiforme (GBM), is grade IV astrocytoma characterized by being fast-growing and the most aggressive brain tumor. In adults, it is the most prevalent type of malignant brain tumor. Despite the advancements in both diagnosis tools and therapeutic treatments, GBM is still associated with poor survival rate without any statistically significant improvement in the past three decades. Patient's genome signature is one of the key factors causing the development of this tumor, in addition to previous radiation exposure and other environmental factors. Researchers have identified genomic and subsequent molecular alterations affecting core pathways that trigger the malignant phenotype of this tumor. Targeting intrinsically altered molecules and pathways is seen as a novel avenue in GBM treatment. The present review shed light on signaling pathways and intrinsically altered molecules implicated in GBM development. It discussed the main challenges impeding successful GBM treatment, such as the blood brain barrier and tumor microenvironment (TME), the plasticity and heterogeneity of both GBM and TME and the glioblastoma stem cells. The present review also presented current advancements in GBM molecular targeted therapy in clinical trials. Profound and comprehensive understanding of molecular participants opens doors for innovative, more targeted and personalized GBM therapeutic modalities.

摘要

胶质母细胞瘤,也称为多形性胶质母细胞瘤(GBM),是一种IV级星形细胞瘤,其特征是生长迅速,是最具侵袭性的脑肿瘤。在成年人中,它是最常见的恶性脑肿瘤类型。尽管诊断工具和治疗方法都有了进步,但在过去三十年中,GBM的生存率仍然很低,且没有任何统计学上的显著改善。除了先前的辐射暴露和其他环境因素外,患者的基因组特征是导致这种肿瘤发生的关键因素之一。研究人员已经确定了影响核心通路的基因组及后续分子改变,这些改变引发了该肿瘤的恶性表型。针对内在改变的分子和通路被视为GBM治疗的新途径。本综述揭示了与GBM发生相关的信号通路和内在改变的分子。它讨论了阻碍GBM成功治疗的主要挑战,如血脑屏障和肿瘤微环境(TME)、GBM和TME的可塑性和异质性以及胶质母细胞瘤干细胞。本综述还介绍了GBM分子靶向治疗在临床试验中的当前进展。对分子参与者的深刻而全面的理解为创新、更具针对性和个性化的GBM治疗模式打开了大门。