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溶瘤治疗的未来前景。

Future prospects for oncolytic therapy.

作者信息

McCormick Frank

机构信息

University of California San Francisco, Cancer Research Institute, CA 94115, USA.

出版信息

Oncogene. 2005 Nov 21;24(52):7817-9. doi: 10.1038/sj.onc.1209064.

DOI:10.1038/sj.onc.1209064
PMID:16299540
Abstract

Viruses have been engineered to replicate selectively in cancer cells, based on a number of innovative principles. Several of these viruses have entered clinical trials and have proven relatively safe, and have shown evidence of efficacy. However, further research is required to enable these agents to function systemically. This might involve attempts to suppress immune responses to virus antigens, and re-targeting of viruses to favor tumor infection and increased potency. When these barriers are overcome, oncolytic viruses could enter the mainstream of clinical oncology.

摘要

基于一些创新原理,病毒已被设计成可在癌细胞中选择性复制。其中几种病毒已进入临床试验,且已证明相对安全,并显示出疗效证据。然而,需要进一步研究以使这些制剂能够在全身发挥作用。这可能涉及抑制对病毒抗原的免疫反应,以及重新靶向病毒以促进肿瘤感染并提高效力。当这些障碍被克服时,溶瘤病毒可能会进入临床肿瘤学的主流。

相似文献

1
Future prospects for oncolytic therapy.溶瘤治疗的未来前景。
Oncogene. 2005 Nov 21;24(52):7817-9. doi: 10.1038/sj.onc.1209064.
2
ReVOLT: radiation-enhanced viral oncolytic therapy.ReVOLT:辐射增强型病毒溶瘤疗法
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Virus combinations and chemotherapy for the treatment of human cancers.用于治疗人类癌症的病毒组合与化疗
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Viruses - seeking and destroying the tumor program.病毒——寻找并摧毁肿瘤程序。
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To replicate or not to replicate: achieving selective oncolytic virus replication in cancer cells through translational control.复制还是不复制:通过翻译控制实现溶瘤病毒在癌细胞中的选择性复制。
Oncogene. 2005 Nov 21;24(52):7697-709. doi: 10.1038/sj.onc.1209053.
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Luciferase imaging for evaluation of oncolytic adenovirus replication in vivo.用于评估溶瘤腺病毒体内复制的荧光素酶成像
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[Oncolytic virus therapy for malignant brain tumors].[溶瘤病毒疗法治疗恶性脑肿瘤]
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Oncolytic adenoviruses - selective retargeting to tumor cells.溶瘤腺病毒——选择性重定向至肿瘤细胞
Oncogene. 2005 Nov 21;24(52):7775-91. doi: 10.1038/sj.onc.1209044.

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Complex spatial dynamics of oncolytic viruses in vitro: mathematical and experimental approaches.体外溶瘤病毒的复杂空间动力学:数学和实验方法。
PLoS Comput Biol. 2012;8(6):e1002547. doi: 10.1371/journal.pcbi.1002547. Epub 2012 Jun 14.
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Oncolytic adenovirus expressing soluble TGFβ receptor II-Fc-mediated inhibition of established bone metastases: a safe and effective systemic therapeutic approach for breast cancer.表达可溶性 TGFβ 受体 II-Fc 的溶瘤腺病毒抑制已建立的骨转移:一种用于乳腺癌的安全有效的系统治疗方法。
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Systemic delivery of a novel liver-detargeted oncolytic adenovirus causes reduced liver toxicity but maintains the antitumor response in a breast cancer bone metastasis model.新型肝脏靶向溶瘤腺病毒的全身递送可降低肝脏毒性,同时在乳腺癌骨转移模型中保持抗肿瘤反应。
Hum Gene Ther. 2011 Sep;22(9):1137-42. doi: 10.1089/hum.2011.003. Epub 2011 Jun 8.
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Systemic delivery of an oncolytic adenovirus expressing soluble transforming growth factor-β receptor II-Fc fusion protein can inhibit breast cancer bone metastasis in a mouse model.表达可溶性转化生长因子-β受体II-Fc融合蛋白的溶瘤腺病毒的全身递送可在小鼠模型中抑制乳腺癌骨转移。
Hum Gene Ther. 2010 Nov;21(11):1623-9. doi: 10.1089/hum.2010.018. Epub 2010 Sep 9.
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The viral tropism of two distinct oncolytic viruses, reovirus and myxoma virus, is modulated by cellular tumor suppressor gene status.两种不同溶瘤病毒(呼肠孤病毒和兔粘液瘤病毒)的病毒趋向性受细胞肿瘤抑制基因状态的调节。
Oncogene. 2010 Jul 8;29(27):3990-6. doi: 10.1038/onc.2010.137. Epub 2010 May 17.
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ODE models for oncolytic virus dynamics.溶瘤病毒动力学的 ODE 模型。
J Theor Biol. 2010 Apr 21;263(4):530-43. doi: 10.1016/j.jtbi.2010.01.009. Epub 2010 Jan 18.
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A modified hTERT promoter-directed oncolytic adenovirus replication with concurrent inhibition of TGFbeta signaling for breast cancer therapy.一种经改良的 hTERT 启动子指导的溶瘤腺病毒复制,同时抑制 TGFβ 信号通路,用于乳腺癌治疗。
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Towards predictive computational models of oncolytic virus therapy: basis for experimental validation and model selection.走向溶瘤病毒治疗的预测性计算模型:实验验证和模型选择的基础
PLoS One. 2009;4(1):e4271. doi: 10.1371/journal.pone.0004271. Epub 2009 Jan 30.