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恶性胶质瘤的化疗及新型治疗方法

Chemotherapy and novel therapeutic approaches in malignant glioma.

作者信息

Desjardins Annick, Rich Jeremy N, Quinn Jennifer A, Vredenburgh James, Gururangan Sridharan, Sathornsumetee Sith, Reardon David A, Friedman Allan H, Bigner Darell D, Friedman Henry S

机构信息

The Brain Tumor Center, Department of Pediatrics, Duke University Medical Center, 047 Baker House, Trent Drive, Box 3624, Durham, NC 27710, USA.

出版信息

Front Biosci. 2005 Sep 1;10:2645-68. doi: 10.2741/1727.

DOI:10.2741/1727
PMID:15970525
Abstract

Glial neoplasms represent 0.5-1% of all cancers in most Western countries. Malignant gliomas are among the most devastating cancers, leading to death in most cases. They present unique challenges due to their location, aggressive biological behavior and diffuse infiltrative growth. Notwithstanding the development of new surgical and radiation techniques in the last thirty years, a cure for malignant gliomas remains elusive. In this article, we will review the standard and new therapies used for malignant gliomas. As standard therapies, surgery, radiation therapy and systemic chemotherapy, are in a continuous process of evolution. Multiple chemotherapies have been used in malignant gliomas, as single agents, in combination, or with different modes of administration, including high-dose chemotherapy with stem cell rescue and intra-arterial chemotherapy. The last decade has been noticeable for the advent of a better understanding of the biology of malignant gliomas. This has stimulated active research in multiples areas and the advent of new treatment strategies. Techniques to circumvent the resistance mechanisms to chemotherapy have been evaluated, tyrosine kinase inhibitors have shown activity in malignant primary brain tumors and radioimmunotherapy remains an area of active research. In this article, we review the past, present and future treatments of malignant gliomas with a special interest on chemotherapy, resistance mechanisms and tyrosine kinase inhibitors.

摘要

在大多数西方国家,神经胶质瘤占所有癌症的0.5%-1%。恶性胶质瘤是最具毁灭性的癌症之一,大多数情况下会导致死亡。由于其位置、侵袭性生物学行为和弥漫性浸润性生长,它们带来了独特的挑战。尽管在过去三十年中出现了新的手术和放疗技术,但恶性胶质瘤的治愈方法仍然难以捉摸。在本文中,我们将回顾用于恶性胶质瘤的标准疗法和新疗法。作为标准疗法,手术、放疗和全身化疗都处于不断发展的过程中。多种化疗药物已用于恶性胶质瘤,作为单一药物、联合使用或采用不同的给药方式,包括高剂量化疗联合干细胞救援和动脉内化疗。过去十年因对恶性胶质瘤生物学有了更好的理解而引人注目。这激发了多个领域的积极研究以及新治疗策略的出现。规避化疗耐药机制的技术已得到评估,酪氨酸激酶抑制剂在恶性原发性脑肿瘤中显示出活性,放射免疫疗法仍然是一个积极研究的领域。在本文中,我们回顾恶性胶质瘤的过去、现在和未来治疗方法,特别关注化疗、耐药机制和酪氨酸激酶抑制剂。

相似文献

1
Chemotherapy and novel therapeutic approaches in malignant glioma.恶性胶质瘤的化疗及新型治疗方法
Front Biosci. 2005 Sep 1;10:2645-68. doi: 10.2741/1727.
2
Current status of local therapy in malignant gliomas--a clinical review of three selected approaches.恶性脑胶质瘤的局部治疗现状——三种选定方法的临床评价。
Pharmacol Ther. 2013 Sep;139(3):341-58. doi: 10.1016/j.pharmthera.2013.05.003. Epub 2013 May 18.
3
Current concepts and newer developments in the treatment of malignant gliomas.恶性胶质瘤治疗的当前概念与新进展
Indian J Cancer. 2009 Apr-Jun;46(2):88-95. doi: 10.4103/0019-509x.49146.
4
Medical treatment of high grade malignant gliomas in adults: an overview.成人高级别恶性胶质瘤的医学治疗:概述
Anticancer Res. 1991 Mar-Apr;11(2):719-27.
5
Management of malignant glioma: steady progress with multimodal approaches.恶性胶质瘤的管理:多模式方法取得稳步进展。
Neurosurg Focus. 2006 Apr 15;20(4):E3.
6
Endovascular therapies for malignant gliomas: Challenges and the future.恶性胶质瘤的血管内治疗:挑战与未来。
J Clin Neurosci. 2016 Apr;26:26-32. doi: 10.1016/j.jocn.2015.10.019. Epub 2016 Feb 5.
7
The role of radiosurgery for glial neoplasms.
Neurosurg Clin N Am. 1999 Apr;10(2):351-8.
8
New frontiers in therapy of malignant gliomas.恶性胶质瘤治疗的新前沿
Forum (Genova). 1998 Jul-Sep;8(3):261-9.
9
Chemotherapy for malignant gliomas.恶性胶质瘤的化疗
Oncology (Williston Park). 1993 Sep;7(9):93-100; discussion 103, 106.
10
Antiangiogenic therapy in malignant glioma: promise and challenge.恶性胶质瘤的抗血管生成治疗:前景与挑战。
Curr Pharm Des. 2007;13(35):3545-58. doi: 10.2174/138161207782794130.

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Cells. 2023 Jul 25;12(15):1921. doi: 10.3390/cells12151921.
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Nomogram Model for Predicting the Prognosis of High-Grade Glioma in Adults Receiving Standard Treatment: A Retrospective Cohort Study.预测接受标准治疗的成人高级别胶质瘤预后的列线图模型:一项回顾性队列研究。
J Clin Med. 2022 Dec 27;12(1):196. doi: 10.3390/jcm12010196.
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Research progress of anti-glioma chemotherapeutic drugs (Review).
抗脑胶质瘤化疗药物的研究进展(综述)。
Oncol Rep. 2022 May;47(5). doi: 10.3892/or.2022.8312. Epub 2022 Apr 1.
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miR-504 modulates the stemness and mesenchymal transition of glioma stem cells and their interaction with microglia via delivery by extracellular vesicles.miR-504 通过细胞外囊泡传递调节神经胶质瘤干细胞的干性和间充质转化及其与小胶质细胞的相互作用。
Cell Death Dis. 2020 Oct 22;11(10):899. doi: 10.1038/s41419-020-03088-3.
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Delivery of Exogenous miR-124 to Glioblastoma Multiform Cells by Wharton's Jelly Mesenchymal Stem Cells Decreases Cell Proliferation and Migration, and Confers Chemosensitivity.间充质干细胞通过牙髓基质传递外源性 miR-124 可降低多形性胶质母细胞瘤细胞的增殖和迁移,并增强化学敏感性。
Stem Cell Rev Rep. 2018 Apr;14(2):236-246. doi: 10.1007/s12015-017-9788-3.
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Human SLFN5 is a transcriptional co-repressor of STAT1-mediated interferon responses and promotes the malignant phenotype in glioblastoma.人类SLFN5是STAT1介导的干扰素反应的转录共抑制因子,并促进胶质母细胞瘤的恶性表型。
Oncogene. 2017 Oct 26;36(43):6006-6019. doi: 10.1038/onc.2017.205. Epub 2017 Jul 3.
7
Guanosine promotes cytotoxicity via adenosine receptors and induces apoptosis in temozolomide-treated A172 glioma cells.鸟苷通过腺苷受体促进细胞毒性,并诱导替莫唑胺处理的 A172 神经胶质瘤细胞凋亡。
Purinergic Signal. 2017 Sep;13(3):305-318. doi: 10.1007/s11302-017-9562-7. Epub 2017 May 23.
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Atorvastatin Promotes Cytotoxicity and Reduces Migration and Proliferation of Human A172 Glioma Cells.阿托伐他汀促进人 A172 神经胶质瘤细胞的细胞毒性,并降低其迁移和增殖能力。
Mol Neurobiol. 2018 Feb;55(2):1509-1523. doi: 10.1007/s12035-017-0423-8. Epub 2017 Feb 8.
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Icaritin induces apoptotic and autophagic cell death in human glioblastoma cells.淫羊藿素诱导人胶质母细胞瘤细胞发生凋亡和自噬性细胞死亡。
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RTVP-1 regulates glioma cell migration and invasion via interaction with N-WASP and hnRNPK.RTVP-1通过与N-WASP和hnRNPK相互作用来调节胶质瘤细胞的迁移和侵袭。
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