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本文引用的文献

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HIF1alpha induces the recruitment of bone marrow-derived vascular modulatory cells to regulate tumor angiogenesis and invasion.缺氧诱导因子1α(HIF1α)诱导骨髓来源的血管调节细胞募集,以调节肿瘤血管生成和侵袭。
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Bevacizumab for recurrent malignant gliomas: efficacy, toxicity, and patterns of recurrence.贝伐单抗治疗复发性恶性胶质瘤:疗效、毒性及复发模式
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A phase I clinical trial of interferon-beta gene therapy for high-grade glioma: novel findings from gene expression profiling and autopsy.一项针对高级别胶质瘤的干扰素-β基因治疗的I期临床试验:基因表达谱分析和尸检的新发现。
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Tumor angiogenic and hypoxic profiles predict radiographic response and survival in malignant astrocytoma patients treated with bevacizumab and irinotecan.肿瘤血管生成和缺氧特征可预测接受贝伐单抗和伊立替康治疗的恶性星形细胞瘤患者的影像学反应和生存情况。
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Cyclooxygenase-2 (Cox-2) expression and angiogenesis in glioblastoma.胶质母细胞瘤中环氧合酶-2(Cox-2)的表达与血管生成
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Pilot study of anti-angiogenic vaccine using fixed whole endothelium in patients with progressive malignancy after failure of conventional therapy.在常规治疗失败后病情进展的恶性肿瘤患者中使用固定全内皮细胞的抗血管生成疫苗的初步研究。
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Tumorigenesis of chemotherapeutic drug-resistant cancer stem-like cells in brain glioma.脑胶质瘤中化疗耐药癌干细胞样细胞的肿瘤发生
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Bevacizumab plus irinotecan in recurrent glioblastoma multiforme.贝伐单抗联合伊立替康治疗复发性多形性胶质母细胞瘤
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脑肿瘤的抗血管生成治疗

Antiangiogenic therapy in brain tumors.

作者信息

Lakka Sajani S, Rao Jasti S

机构信息

Department of Cancer Biology and Pharmacology, University of Illinois College of Medicine at Peoria, 1 Illini Drive, Peoria, IL 61605, USA.

出版信息

Expert Rev Neurother. 2008 Oct;8(10):1457-73. doi: 10.1586/14737175.8.10.1457.

DOI:10.1586/14737175.8.10.1457
PMID:18928341
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2656359/
Abstract

Angiogenesis, the recruitment of new blood vessels, is an essential component of tumor progression. Malignant brain tumors are highly vascularized and their growth is angiogenesis-dependent. As such, inhibition of the sprouting of new capillaries from pre-existing blood vessels is one of the most promising antiglioma therapeutic approaches. Numerous classes of molecules have been implicated in regulating angiogenesis and, thus, novel agents that target and counteract angiogenesis are now being developed. The therapeutic trials of a number of angiogenesis inhibitors as antiglioma drugs are currently under intense investigation. Preliminary studies of angiogenic blockade in glioblastoma have been promising and several clinical trials are now underway to develop optimum treatment strategies for antiangiogenic agents. This review will cover state-of-the-art antiangiogenic targets for brain tumor treatment and discuss future challenges. An increased understanding of the angiogenic process, the diversity of its inducers and mediators, appropriate drug schedules and the use of these agents with other modalities may lead to radically new treatment regimens to achieve maximal efficacy.

摘要

血管生成,即新血管的募集,是肿瘤进展的一个重要组成部分。恶性脑肿瘤血管高度丰富,其生长依赖于血管生成。因此,抑制从现有血管中长出新的毛细血管是最有前景的抗胶质瘤治疗方法之一。许多种类的分子都与血管生成的调节有关,因此,目前正在开发靶向并对抗血管生成的新型药物。目前,多种血管生成抑制剂作为抗胶质瘤药物的治疗试验正在深入研究中。胶质母细胞瘤血管生成阻断的初步研究很有前景,目前正在进行多项临床试验,以制定抗血管生成药物的最佳治疗策略。这篇综述将涵盖脑肿瘤治疗的最新抗血管生成靶点,并讨论未来的挑战。对血管生成过程、其诱导剂和介质的多样性、合适的用药方案以及这些药物与其他治疗方式联合使用的深入理解,可能会带来全新的治疗方案,以实现最大疗效。