• 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

相似文献

1
A phase I/II clinical trial in localized prostate cancer of an adenovirus expressing nitroreductase with CB1954 [correction of CB1984].一项针对局限性前列腺癌的I/II期临床试验,该试验使用一种表达硝基还原酶并联合CB1954[纠正为CB1954]的腺病毒。
Mol Ther. 2009 Jul;17(7):1292-9. doi: 10.1038/mt.2009.80. Epub 2009 Apr 14.
2
Virus-directed enzyme prodrug therapy: intratumoral administration of a replication-deficient adenovirus encoding nitroreductase to patients with resectable liver cancer.病毒导向酶前药疗法:向可切除肝癌患者瘤内注射编码硝基还原酶的复制缺陷型腺病毒。
J Clin Oncol. 2004 May 1;22(9):1546-52. doi: 10.1200/JCO.2004.10.005. Epub 2004 Mar 29.
3
Combined adenovirus-mediated nitroreductase gene delivery and CB1954 treatment: a well-tolerated therapy for established solid tumors.腺病毒介导的硝基还原酶基因递送与CB1954联合治疗:一种对已形成实体瘤耐受性良好的疗法。
Mol Ther. 2001 Feb;3(2):233-40. doi: 10.1006/mthe.2000.0250.
4
Late expression of nitroreductase in an oncolytic adenovirus sensitizes colon cancer cells to the prodrug CB1954.溶瘤腺病毒中硝基还原酶的晚期表达使结肠癌细胞对前药CB1954敏感。
Hum Gene Ther. 2005 Dec;16(12):1473-83. doi: 10.1089/hum.2005.16.1473.
5
Antivector and tumor immune responses following adenovirus-directed enzyme prodrug therapy for the treatment of prostate cancer.腺病毒导向酶前药治疗前列腺癌后的抗载体和肿瘤免疫反应。
Hum Gene Ther. 2009 Nov;20(11):1249-58. doi: 10.1089/hum.2009.078.
6
Virus-directed, enzyme prodrug therapy with nitroimidazole reductase: a phase I and pharmacokinetic study of its prodrug, CB1954.病毒导向的、含硝基咪唑还原酶的酶前体药物疗法:其前体药物CB1954的I期及药代动力学研究
Clin Cancer Res. 2001 Sep;7(9):2662-8.
7
Nitroreductase: a prodrug-activating enzyme for cancer gene therapy.硝基还原酶:一种用于癌症基因治疗的前药激活酶。
Clin Exp Pharmacol Physiol. 2004 Nov;31(11):811-6. doi: 10.1111/j.1440-1681.2004.04085.x.
8
Sensitisation of human carcinoma cells to the prodrug CB1954 by adenovirus vector-mediated expression of E. coli nitroreductase.通过腺病毒载体介导的大肠杆菌硝基还原酶表达使人类癌细胞对前药CB1954致敏。
Int J Cancer. 2000 Jun 15;86(6):848-54. doi: 10.1002/(sici)1097-0215(20000615)86:6<848::aid-ijc14>3.0.co;2-b.
9
E. coli NfsA: an alternative nitroreductase for prodrug activation gene therapy in combination with CB1954.大肠杆菌NfsA:一种与CB1954联合用于前药激活基因治疗的替代硝基还原酶。
Br J Cancer. 2009 Jun 16;100(12):1903-11. doi: 10.1038/sj.bjc.6605094. Epub 2009 May 19.
10
Enhanced efficacy of Escherichia coli nitroreductase/CB1954 prodrug activation gene therapy using an E1B-55K-deleted oncolytic adenovirus vector.使用缺失E1B-55K的溶瘤腺病毒载体增强大肠杆菌硝基还原酶/CB1954前药激活基因疗法的疗效。
Gene Ther. 2004 Jul;11(14):1126-36. doi: 10.1038/sj.gt.3302271.

引用本文的文献

1
Programming tumor evolution with selection gene drives to proactively combat drug resistance.利用选择基因驱动对肿瘤进化进行编程,以主动对抗耐药性。
Nat Biotechnol. 2025 May;43(5):737-751. doi: 10.1038/s41587-024-02271-7. Epub 2024 Jul 4.
2
Structural Evaluation of a Nitroreductase Engineered for Improved Activation of the 5-Nitroimidazole PET Probe SN33623.用于改善 5-硝基咪唑 PET 探针 SN33623 激活的硝基还原酶工程的结构评估。
Int J Mol Sci. 2024 Jun 15;25(12):6593. doi: 10.3390/ijms25126593.
3
Structure and Dynamics of Three NfsB Nitro-Reductase Mutants Selected for Enhanced Activity with the Cancer Prodrug CB1954.三种 NfsB 硝基还原酶突变体的结构与动力学研究,这些突变体是为了提高癌症前药 CB1954 的活性而选择的。
Int J Mol Sci. 2023 Mar 22;24(6):5987. doi: 10.3390/ijms24065987.
4
Engineering the Nitroreductase NfsA to Create a Flexible Enzyme-Prodrug Activation System.工程改造硝基还原酶NfsA以创建一个灵活的酶-前药激活系统。
Front Pharmacol. 2021 Jun 7;12:701456. doi: 10.3389/fphar.2021.701456. eCollection 2021.
5
The YfkO Nitroreductase from Bacillus Licheniformis on Gold-Coated Superparamagnetic Nanoparticles: Towards a Novel Directed Enzyme Prodrug Therapy Approach.来自地衣芽孢杆菌的YfkO硝基还原酶负载于金包被超顺磁性纳米颗粒上:迈向一种新型的定向酶前药治疗方法。
Pharmaceutics. 2021 Apr 9;13(4):517. doi: 10.3390/pharmaceutics13040517.
6
Repurposing F-FMISO as a PET tracer for translational imaging of nitroreductase-based gene directed enzyme prodrug therapy.将F-FMISO重新用作正电子发射断层显像(PET)示踪剂,用于基于硝基还原酶的基因导向酶前药疗法的转化成像。
Theranostics. 2021 Apr 7;11(12):6044-6057. doi: 10.7150/thno.55092. eCollection 2021.
7
Prodrugs and prodrug-activated systems in gene therapy.基因治疗中的前药和前药激活系统。
Mol Ther. 2021 May 5;29(5):1716-1728. doi: 10.1016/j.ymthe.2021.04.006. Epub 2021 Apr 6.
8
Evolutionary aspects of the Viridiplantae nitroreductases.绿色植物亚界(Viridiplantae)中硝基还原酶的进化方面。
J Genet Eng Biotechnol. 2020 Oct 6;18(1):60. doi: 10.1186/s43141-020-00073-3.
9
Evaluation of two xenobiotic reductases from Pseudomonas putida for their suitability for magnetic nanoparticle-directed enzyme prodrug therapy as a novel approach to cancer treatment.评价两种来自恶臭假单胞菌的异种生物还原酶,以评估其作为癌症治疗新方法的磁性纳米颗粒导向酶前药治疗的适用性。
Microbiologyopen. 2020 Oct;9(10):e1110. doi: 10.1002/mbo3.1110. Epub 2020 Sep 26.
10
Extracellular Vesicle-Mediated Transcribed mRNA Delivery for Treatment of HER2 Breast Cancer Xenografts in Mice by Prodrug CB1954 without General Toxicity.外泌体介导的转录 mRNA 递送来治疗荷 HER2 乳腺癌小鼠异种移植瘤,使用前药 CB1954 治疗没有一般毒性。
Mol Cancer Ther. 2020 Mar;19(3):858-867. doi: 10.1158/1535-7163.MCT-19-0928. Epub 2020 Jan 15.

本文引用的文献

1
Cancer statistics, 2006.2006年癌症统计数据。
CA Cancer J Clin. 2006 Mar-Apr;56(2):106-30. doi: 10.3322/canjclin.56.2.106.
2
Biological response determinants in HSV-tk + ganciclovir gene therapy for prostate cancer.单纯疱疹病毒胸苷激酶基因联合更昔洛韦治疗前列腺癌中的生物学反应决定因素
Mol Ther. 2006 Apr;13(4):716-28. doi: 10.1016/j.ymthe.2005.11.022. Epub 2006 Feb 15.
3
Expanding the therapeutic index of radiation therapy by combining in situ gene therapy in the treatment of prostate cancer.通过在前列腺癌治疗中联合原位基因治疗来扩大放射治疗的治疗指数。
Technol Cancer Res Treat. 2006 Feb;5(1):23-36. doi: 10.1177/153303460600500104.
4
Virus specific immune responses after human neoadjuvant adenovirus-mediated suicide gene therapy for prostate cancer.人新辅助腺病毒介导的自杀基因疗法治疗前列腺癌后的病毒特异性免疫反应
Eur Urol. 2005 Jul;48(1):153-61. doi: 10.1016/j.eururo.2005.02.013. Epub 2005 Mar 9.
5
Oncolytic adenovirus CG7870 in combination with radiation demonstrates synergistic enhancements of antitumor efficacy without loss of specificity.溶瘤腺病毒CG7870与放疗联合使用可协同增强抗肿瘤疗效,且不丧失特异性。
Cancer Gene Ther. 2005 Aug;12(8):715-22. doi: 10.1038/sj.cgt.7700835.
6
Evidence that transfer of functional p53 protein results in increased apoptosis in prostate cancer.功能性p53蛋白转移导致前列腺癌细胞凋亡增加的证据。
Clin Cancer Res. 2004 Apr 15;10(8):2587-93. doi: 10.1158/1078-0432.ccr-03-0388.
7
Virus-directed enzyme prodrug therapy: intratumoral administration of a replication-deficient adenovirus encoding nitroreductase to patients with resectable liver cancer.病毒导向酶前药疗法:向可切除肝癌患者瘤内注射编码硝基还原酶的复制缺陷型腺病毒。
J Clin Oncol. 2004 May 1;22(9):1546-52. doi: 10.1200/JCO.2004.10.005. Epub 2004 Mar 29.
8
Phase I-II trial evaluating combined intensity-modulated radiotherapy and in situ gene therapy with or without hormonal therapy in treatment of prostate cancer-interim report on PSA response and biopsy data.评估调强放疗联合原位基因治疗加或不加激素治疗前列腺癌的I-II期试验——前列腺特异抗原反应及活检数据中期报告
Int J Radiat Oncol Biol Phys. 2004 Apr 1;58(5):1520-9. doi: 10.1016/j.ijrobp.2003.09.083.
9
Eligibility and outcomes reporting guidelines for clinical trials for patients in the state of a rising prostate-specific antigen: recommendations from the Prostate-Specific Antigen Working Group.前列腺特异性抗原升高状态患者临床试验的入选标准及结果报告指南:前列腺特异性抗原工作组的建议
J Clin Oncol. 2004 Feb 1;22(3):537-56. doi: 10.1200/JCO.2004.07.099.
10
Prostate-specific antigen doubling time in the identification of patients at risk for progression after treatment and biochemical recurrence for prostate cancer.前列腺特异性抗原倍增时间在识别前列腺癌治疗后进展风险及生化复发患者中的应用
Urology. 2003 Dec 29;62 Suppl 1:2-8. doi: 10.1016/j.urology.2003.09.009.

一项针对局限性前列腺癌的I/II期临床试验,该试验使用一种表达硝基还原酶并联合CB1954[纠正为CB1954]的腺病毒。

A phase I/II clinical trial in localized prostate cancer of an adenovirus expressing nitroreductase with CB1954 [correction of CB1984].

作者信息

Patel Prashant, Young J Graham, Mautner Vivien, Ashdown Daniel, Bonney Sarah, Pineda Robert G, Collins Stuart I, Searle Peter F, Hull Diana, Peers Elizabeth, Chester John, Wallace D Michael, Doherty Alan, Leung Hing, Young Lawrence S, James Nicholas D

机构信息

CR UK Institute for Cancer Studies, University of Birmingham, UK.

出版信息

Mol Ther. 2009 Jul;17(7):1292-9. doi: 10.1038/mt.2009.80. Epub 2009 Apr 14.

DOI:10.1038/mt.2009.80
PMID:19367257
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2835198/
Abstract

We report a phase I/II clinical trial in prostate cancer (PCa) using direct intraprostatic injection of a replication defective adenovirus vector (CTL102) encoding bacterial nitroreductase (NTR) in conjunction with systemic prodrug CB1954. One group of patients with localized PCa scheduled for radical prostatectomy received virus alone, prior to surgery, in a dose escalation to establish safety, tolerability, and NTR expression. A second group with local failure following primary treatment received virus plus prodrug to establish safety and tolerability. Based on acceptable safety data and indications of prostate-specific antigen (PSA) responses, an extended cohort received virus at a single dose level plus prodrug. The vector was well tolerated with minimal side effects, had a short half-life in the circulation, and stimulated a robust antibody response. Immunohistochemistry of resected prostate demonstrated NTR staining in tumor and glandular epithelium at all dose levels [5 x 10(10)-1 x 10(12) virus particles (vp)]. A total of 19 patients received virus plus prodrug and 14 of these had a repeat treatment; minimal toxicity was observed and there was preliminary evidence of change in PSA kinetics, with an increase in the time to 10% PSA progression in 6 out of 18 patients at 6 months.

摘要

我们报告了一项针对前列腺癌(PCa)的I/II期临床试验,该试验采用直接前列腺内注射编码细菌硝基还原酶(NTR)的复制缺陷型腺病毒载体(CTL102)并联合全身使用前药CB1954。一组计划进行根治性前列腺切除术的局限性PCa患者在手术前单独接受病毒注射,剂量逐步递增以确定安全性、耐受性和NTR表达情况。第二组在初次治疗后出现局部失败的患者接受病毒加前药治疗,以确定安全性和耐受性。基于可接受的安全性数据和前列腺特异性抗原(PSA)反应的迹象,一个扩大队列接受了单剂量水平的病毒加前药治疗。该载体耐受性良好,副作用极小,在循环中的半衰期较短,并刺激了强烈的抗体反应。切除前列腺的免疫组织化学显示,在所有剂量水平[5×10(10)-1×10(12)病毒颗粒(vp)]下,肿瘤和腺上皮中均有NTR染色。共有19名患者接受了病毒加前药治疗,其中14名患者接受了重复治疗;观察到的毒性极小,并且有初步证据表明PSA动力学发生了变化,在6个月时,18名患者中有6名患者的PSA进展至10%的时间有所延长。