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A robust approach to enhance tumor-selective accumulation of nanoparticles.一种增强纳米颗粒肿瘤选择性聚集的可靠方法。
Oncotarget. 2011 Jan-Feb;2(1-2):59-68. doi: 10.18632/oncotarget.227.
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FLIP regulation of HO-1 and TNF signalling in human acute myeloid leukemia provides a unique secondary anti-apoptotic mechanism.人急性髓系白血病中FLIP对HO-1和TNF信号的调节提供了一种独特的继发性抗凋亡机制。
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The heme oxygenase-1 and c-FLIP in acute myeloid leukemias: two non-redundant but mutually exclusive cellular safeguards protecting cells against TNF-induced cell death?急性髓系白血病中的血红素加氧酶-1和c-FLIP:两种非冗余但相互排斥的细胞保护机制可保护细胞免受肿瘤坏死因子诱导的细胞死亡?
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Tumor necrosis factor-α signaling in macrophages.巨噬细胞中的肿瘤坏死因子-α信号传导
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Transmembrane TNF-alpha: structure, function and interaction with anti-TNF agents.跨膜 TNF-α:结构、功能及与抗 TNF 制剂的相互作用。
Rheumatology (Oxford). 2010 Jul;49(7):1215-28. doi: 10.1093/rheumatology/keq031. Epub 2010 Mar 1.
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Preclinical investigation of PEGylated tumor necrosis factor alpha in dogs with spontaneous tumors: phase I evaluation.PEG 化肿瘤坏死因子 α 在患有自发性肿瘤的犬中的临床前研究:I 期评估。
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Phase Ib study of NGR-hTNF, a selective vascular targeting agent, administered at low doses in combination with doxorubicin to patients with advanced solid tumours.NGR-hTNF(一种选择性血管靶向剂)低剂量与阿霉素联合应用于晚期实体瘤患者的Ib期研究。
Br J Cancer. 2009 Jul 21;101(2):219-24. doi: 10.1038/sj.bjc.6605162. Epub 2009 Jun 30.
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Tumour necrosis factor and cancer.肿瘤坏死因子与癌症
Nat Rev Cancer. 2009 May;9(5):361-71. doi: 10.1038/nrc2628. Epub 2009 Apr 3.
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Phase 2 trial of recombinant tumor necrosis factor-alpha in combination with dactinomycin in children with recurrent Wilms tumor.重组肿瘤坏死因子-α联合放线菌素D治疗儿童复发性肾母细胞瘤的2期试验
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The neovasculature homing motif NGR: more than meets the eye.新生血管归巢基序NGR:不止于所见。
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将肿瘤坏死因子α作为抗癌剂进行全身应用。

Systemic use of tumor necrosis factor alpha as an anticancer agent.

作者信息

Roberts Nicholas J, Zhou Shibin, Diaz Luis A, Holdhoff Matthias

机构信息

Ludwig Center for Cancer Genetics and Therapeutics, The Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University, Baltimore, MD 21231, USA.

出版信息

Oncotarget. 2011 Oct;2(10):739-51. doi: 10.18632/oncotarget.344.

DOI:10.18632/oncotarget.344
PMID:22036896
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3248159/
Abstract

Tumor necrosis factor-α (TNF-α) has been discussed as a potential anticancer agent for many years, however initial enthusiasm about its clinical use as a systemic agent was curbed due to significant toxicities and lack of efficacy. Combination of TNF-α with chemotherapy in the setting of hyperthermic isolated limb perfusion (ILP), has provided new insights into a potential therapeutic role of this agent. The therapeutic benefit from TNF-α in ILP is thought to be not only due to its direct anti-proliferative effect, but also due to its ability to increase penetration of the chemotherapeutic agents into the tumor tissue. New concepts for the use of TNF-α as a facilitator rather than as a direct actor are currently being explored with the goal to exploit the ability of this agent to increase drug delivery and to simultaneously reduce systemic toxicity. This review article provides a comprehensive overview on the published previous experience with systemic TNF-α. Data from 18 phase I and 10 phase II single agent as well as 18 combination therapy studies illustrate previously used treatment and dose schedules, response data as well as the most prominently observed adverse effects. Also discussed, based on recent preclinical data, is a potential future role of systemic TNF-α in combination with liposomal chemotherapy to facilitate increased drug uptake into tumors.

摘要

多年来,肿瘤坏死因子-α(TNF-α)一直被视为一种潜在的抗癌药物,然而,由于其显著的毒性和疗效欠佳,人们最初对其作为全身用药的临床应用热情有所减退。在热灌注隔离肢体(ILP)的情况下,将TNF-α与化疗联合使用,为该药物的潜在治疗作用提供了新的见解。TNF-α在ILP中的治疗益处被认为不仅归因于其直接的抗增殖作用,还归因于其增加化疗药物渗透到肿瘤组织中的能力。目前正在探索将TNF-α用作促进剂而非直接作用剂的新概念,目的是利用该药物增加药物递送并同时降低全身毒性的能力。这篇综述文章全面概述了以往关于全身应用TNF-α的经验。来自18项I期和10项II期单药治疗以及18项联合治疗研究的数据说明了先前使用的治疗方法和剂量方案、反应数据以及最显著观察到的不良反应。基于最近的临床前数据,还讨论了全身应用TNF-α与脂质体化疗联合使用以促进肿瘤药物摄取增加的潜在未来作用。