• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

多形性胶质母细胞瘤(GBM)的耐药机制及当前治疗选择

Mechanisms of Resistance and Current Treatment Options for Glioblastoma Multiforme (GBM).

作者信息

Yalamarty Satya Siva Kishan, Filipczak Nina, Li Xiang, Subhan Md Abdus, Parveen Farzana, Ataide Janaína Artem, Rajmalani Bharat Ashok, Torchilin Vladimir P

机构信息

Center for Pharmaceutical Biotechnology and Nanomedicine (CPBN), Department of Pharmaceutical Sciences, Northeastern University, Boston, MA 02115, USA.

State Key Laboratory of Innovative Drug and Efficient Energy-Saving Pharmaceutical Equipment, Jiangxi University of Chinese Medicine, Nanchang 330006, China.

出版信息

Cancers (Basel). 2023 Apr 1;15(7):2116. doi: 10.3390/cancers15072116.

DOI:10.3390/cancers15072116
PMID:37046777
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10093719/
Abstract

Glioblastoma multiforme (GBM) is a highly aggressive form of brain cancer that is difficult to treat due to its resistance to both radiation and chemotherapy. This resistance is largely due to the unique biology of GBM cells, which can evade the effects of conventional treatments through mechanisms such as increased resistance to cell death and rapid regeneration of cancerous cells. Additionally, the blood-brain barrier makes it difficult for chemotherapy drugs to reach GBM cells, leading to reduced effectiveness. Despite these challenges, there are several treatment options available for GBM. The standard of care for newly diagnosed GBM patients involves surgical resection followed by concurrent chemoradiotherapy and adjuvant chemotherapy. Emerging treatments include immunotherapy, such as checkpoint inhibitors, and targeted therapies, such as bevacizumab, that attempt to attack specific vulnerabilities in GBM cells. Another promising approach is the use of tumor-treating fields, a type of electric field therapy that has been shown to slow the growth of GBM cells. Clinical trials are ongoing to evaluate the safety and efficacy of these and other innovative treatments for GBM, intending to improve with outcomes for patients.

摘要

多形性胶质母细胞瘤(GBM)是一种极具侵袭性的脑癌,由于其对放疗和化疗均具有抗性,因而难以治疗。这种抗性很大程度上归因于GBM细胞独特的生物学特性,这些细胞能够通过诸如增强对细胞死亡的抗性以及癌细胞快速再生等机制来逃避传统治疗的影响。此外,血脑屏障使得化疗药物难以抵达GBM细胞,导致疗效降低。尽管存在这些挑战,但GBM仍有多种治疗选择。新诊断的GBM患者的标准治疗方案包括手术切除,随后进行同步放化疗和辅助化疗。新兴治疗方法包括免疫疗法,如检查点抑制剂,以及靶向疗法,如贝伐单抗,它们试图攻击GBM细胞中的特定弱点。另一种有前景的方法是使用肿瘤治疗电场,这是一种电场疗法,已被证明能减缓GBM细胞的生长。目前正在进行临床试验,以评估这些以及其他针对GBM的创新治疗方法的安全性和疗效,旨在改善患者的治疗结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bdd/10093719/f8efe19b7328/cancers-15-02116-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bdd/10093719/5e40c6940451/cancers-15-02116-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bdd/10093719/ac5ea4ddcbe0/cancers-15-02116-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bdd/10093719/f8efe19b7328/cancers-15-02116-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bdd/10093719/5e40c6940451/cancers-15-02116-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bdd/10093719/ac5ea4ddcbe0/cancers-15-02116-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bdd/10093719/f8efe19b7328/cancers-15-02116-g003.jpg

相似文献

1
Mechanisms of Resistance and Current Treatment Options for Glioblastoma Multiforme (GBM).多形性胶质母细胞瘤(GBM)的耐药机制及当前治疗选择
Cancers (Basel). 2023 Apr 1;15(7):2116. doi: 10.3390/cancers15072116.
2
Enhancement of Therapies for Glioblastoma (GBM) Using Nanoparticle-based Delivery Systems.利用基于纳米颗粒的递药系统增强胶质母细胞瘤(GBM)的治疗效果。
AAPS PharmSciTech. 2021 Feb 11;22(2):71. doi: 10.1208/s12249-021-01928-9.
3
Topics in chemotherapy, molecular-targeted therapy, and immunotherapy for newly-diagnosed glioblastoma multiforme.新诊断多形性胶质母细胞瘤的化疗、分子靶向治疗及免疫治疗相关主题
Anticancer Res. 2015 Mar;35(3):1229-35.
4
Advanced biomaterials for human glioblastoma multiforme (GBM) drug delivery.用于人多形性胶质母细胞瘤(GBM)药物递送的先进生物材料。
Biomater Sci. 2023 Jun 13;11(12):4094-4131. doi: 10.1039/d2bm01996e.
5
Combinatorial approaches to effective therapy in glioblastoma (GBM): Current status and what the future holds.胶质母细胞瘤(GBM)有效治疗的组合方法:现状和未来前景。
Int Rev Immunol. 2022;41(6):582-605. doi: 10.1080/08830185.2022.2101647. Epub 2022 Aug 8.
6
Glioblastoma Multiforme-A Look at the Past and a Glance at the Future.多形性胶质母细胞瘤——回顾过去与展望未来
Pharmaceutics. 2021 Jul 9;13(7):1053. doi: 10.3390/pharmaceutics13071053.
7
Advances in Experimental Targeted Therapy and Immunotherapy for Patients with Glioblastoma Multiforme.多形性胶质母细胞瘤患者实验性靶向治疗和免疫治疗的进展
Anticancer Res. 2017 Jan;37(1):21-33. doi: 10.21873/anticanres.11285.
8
Recent Advances in the Therapeutic Strategies of Glioblastoma Multiforme.胶质母细胞瘤治疗策略的最新进展。
Neuroscience. 2022 May 21;491:240-270. doi: 10.1016/j.neuroscience.2022.03.030. Epub 2022 Apr 6.
9
Advances in immunotherapy for glioblastoma multiforme.胶质母细胞瘤的免疫治疗进展。
Front Immunol. 2022 Oct 12;13:944452. doi: 10.3389/fimmu.2022.944452. eCollection 2022.
10
Combination immunotherapy strategies for glioblastoma.胶质母细胞瘤的联合免疫治疗策略。
J Neurooncol. 2021 Feb;151(3):375-391. doi: 10.1007/s11060-020-03481-0. Epub 2021 Feb 21.

引用本文的文献

1
Progenitor cells, microglia, and non-coding RNAs: Orchestrators of glioblastoma pathogenesis and therapeutic resistance.祖细胞、小胶质细胞与非编码RNA:胶质母细胞瘤发病机制及治疗耐药性的调控者
Noncoding RNA Res. 2025 Aug 5;15:85-99. doi: 10.1016/j.ncrna.2025.07.007. eCollection 2025 Dec.
2
Glioblastoma: A Multidisciplinary Approach to Its Pathophysiology, Treatment, and Innovative Therapeutic Strategies.胶质母细胞瘤:关于其病理生理学、治疗及创新治疗策略的多学科方法
Biomedicines. 2025 Aug 2;13(8):1882. doi: 10.3390/biomedicines13081882.
3
Targeting the Kynureninase-HDAC6-Complement Axis as a Novel Therapeutic Strategy in Glioblastoma.

本文引用的文献

1
Tyrosine Kinase Inhibitors for Glioblastoma Multiforme: Challenges and Opportunities for Drug Delivery.用于多形性胶质母细胞瘤的酪氨酸激酶抑制剂:药物递送的挑战与机遇
Pharmaceutics. 2022 Dec 24;15(1):59. doi: 10.3390/pharmaceutics15010059.
2
Strategies to overcome/penetrate the BBB for systemic nanoparticle delivery to the brain/brain tumor.克服/穿透血脑屏障以实现系统纳米颗粒向脑/脑肿瘤递药的策略。
Adv Drug Deliv Rev. 2022 Dec;191:114619. doi: 10.1016/j.addr.2022.114619. Epub 2022 Nov 11.
3
Chronic convection-enhanced delivery of topotecan for patients with recurrent glioblastoma: a first-in-patient, single-centre, single-arm, phase 1b trial.
靶向犬尿氨酸酶-HDAC6-补体轴作为胶质母细胞瘤的一种新型治疗策略
Epigenomes. 2025 Jul 28;9(3):27. doi: 10.3390/epigenomes9030027.
4
Physical activity and glioblastoma: a paradigm shift in neuro-oncology therapy.体育活动与胶质母细胞瘤:神经肿瘤学治疗的范式转变
Front Oncol. 2025 Jul 30;15:1638060. doi: 10.3389/fonc.2025.1638060. eCollection 2025.
5
Graphene quantum dot-integrated nanocomposites: a promising avenue for glioblastoma treatment.石墨烯量子点集成纳米复合材料:胶质母细胞瘤治疗的一条有前景的途径。
Med Oncol. 2025 Aug 8;42(9):417. doi: 10.1007/s12032-025-02967-z.
6
Advanced nanotheranostic approaches for targeted glioblastoma treatment: a synergistic fusion of CRISPR-Cas gene editing, AI-driven tumor profiling, and BBB-modulation.用于靶向胶质母细胞瘤治疗的先进纳米诊疗方法:CRISPR-Cas基因编辑、人工智能驱动的肿瘤分析和血脑屏障调节的协同融合。
Med Oncol. 2025 Aug 7;42(9):413. doi: 10.1007/s12032-025-02944-6.
7
Harnessing immunotherapy: cancer vaccines as novel therapeutic strategies for brain tumor.利用免疫疗法:癌症疫苗作为脑肿瘤的新型治疗策略
Front Immunol. 2025 Jul 17;16:1588081. doi: 10.3389/fimmu.2025.1588081. eCollection 2025.
8
Repurposed Antipsychotics as Potential Anticancer Agents: Clozapine Efficacy and Dopaminergic Pathways in Neuroblastoma and Glioblastoma.重新利用抗精神病药物作为潜在抗癌剂:氯氮平在神经母细胞瘤和胶质母细胞瘤中的疗效及多巴胺能通路
Life (Basel). 2025 Jul 12;15(7):1097. doi: 10.3390/life15071097.
9
Glioblastoma: Overview of Proteomic Investigations and Biobank Approaches for the Development of a Multidisciplinary Translational Network.胶质母细胞瘤:蛋白质组学研究及生物样本库方法概述,用于构建多学科转化网络
Cancers (Basel). 2025 Jun 26;17(13):2151. doi: 10.3390/cancers17132151.
10
The role of in regulating proliferation and invasion in U251 glioblastoma cells.在U251胶质母细胞瘤细胞中调节增殖和侵袭的作用。 (原文“of”后面缺少具体内容)
Contemp Oncol (Pozn). 2025;29(2):195-205. doi: 10.5114/wo.2025.150649. Epub 2025 May 12.
替莫唑胺持续恒速静脉输注治疗复发性胶质母细胞瘤患者的Ⅰb 期单臂单中心首例患者临床试验。
Lancet Oncol. 2022 Nov;23(11):1409-1418. doi: 10.1016/S1470-2045(22)00599-X. Epub 2022 Oct 13.
4
Cancer cell autophagy, reprogrammed macrophages, and remodeled vasculature in glioblastoma triggers tumor immunity.胶质母细胞瘤中的癌细胞自噬、重编程的巨噬细胞和重塑的血管触发肿瘤免疫。
Cancer Cell. 2022 Oct 10;40(10):1111-1127.e9. doi: 10.1016/j.ccell.2022.08.014. Epub 2022 Sep 15.
5
Design, Synthesis and Activity of New -Alkyl Tryptophan Functionalized Dendrimeric Peptides against Glioblastoma.新型烷基色氨酸功能化树枝状肽的设计、合成及对神经胶质瘤的活性。
Biomolecules. 2022 Aug 13;12(8):1116. doi: 10.3390/biom12081116.
6
Characteristics and therapeutic strategies of radiation-induced glioma: case series and comprehensive literature review.辐射诱导性脑胶质瘤的特征和治疗策略:病例系列和文献综述。
J Neurooncol. 2022 Sep;159(3):531-538. doi: 10.1007/s11060-022-04090-9. Epub 2022 Aug 3.
7
Current Considerations in the Treatment of Grade 3 Gliomas.目前 3 级神经胶质瘤治疗的相关考虑。
Curr Treat Options Oncol. 2022 Sep;23(9):1219-1232. doi: 10.1007/s11864-022-01000-z. Epub 2022 Aug 1.
8
Role of PARP Inhibitors in Glioblastoma and Perceiving Challenges as Well as Strategies for Successful Clinical Development.PARP抑制剂在胶质母细胞瘤中的作用以及认识挑战和成功临床开发的策略。
Front Pharmacol. 2022 Jul 6;13:939570. doi: 10.3389/fphar.2022.939570. eCollection 2022.
9
Targeted inducible delivery of immunoactivating cytokines reprograms glioblastoma microenvironment and inhibits growth in mouse models.靶向诱导递送免疫激活细胞因子重塑胶质母细胞瘤微环境并抑制小鼠模型中的生长。
Sci Transl Med. 2022 Jul 13;14(653):eabl4106. doi: 10.1126/scitranslmed.abl4106.
10
The complex relationship between integrins and oncolytic herpes Simplex Virus 1 in high-grade glioma therapeutics.整合素与溶瘤单纯疱疹病毒1在高级别胶质瘤治疗中的复杂关系。
Mol Ther Oncolytics. 2022 Jun 6;26:63-75. doi: 10.1016/j.omto.2022.05.013. eCollection 2022 Sep 15.