• 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

新型血管破坏剂在人类系统性白血病和异种移植模型中的连续监测。

Serial monitoring of human systemic and xenograft models of leukemia using a novel vascular disrupting agent.

机构信息

Department of Radiology, Sloan Kettering Institute for Cancer Research, New York, NY, USA.

出版信息

Leukemia. 2012 Aug;26(8):1771-8. doi: 10.1038/leu.2012.48. Epub 2012 Feb 20.

DOI:10.1038/leu.2012.48
PMID:22343591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4626450/
Abstract

Advances in the treatment of acute leukemia have resulted in significantly improved remission rates, although disease relapse poses a significant risk. By utilizing sensitive, non-invasive imaging guidance, detection of early leukemic infiltration and the extent of residual tumor burden after targeted therapy can be expedited, leading to more efficient treatment planning. We demonstrated marked survival benefit and therapeutic efficacy of a new-generation vascular disrupting agent, combretastatin-A1-diphosphate (OXi4503), using reporter gene-imaging technologies and mice systemically administered luc+ and GFP+ human leukemic cells (LCs). Before treatment, homing of double-transduced cells was serially monitored and whole-body cellular distributions were mapped using bioluminescence imaging (BLI). Imaging findings strongly correlated with quantitative GFP expression levels in solid organs/tissues, suggesting that the measured BLI signal provides a highly sensitive and reliable biomarker of tumor tissue burden in systemic leukemic models. Such optical technologies can thereby serve as robust non-invasive imaging tools for preclinical drug discovery and for rapidly screening promising therapeutic agents to establish potency, treatment efficacy and survival advantage. We further show that GFP+ HL-60 cells reside in close proximity to VE-cadherin- and CD31-expressing endothelial cells, suggesting that the perivascular niche may have a critical role in the maintenance and survival of LCs.

摘要

急性白血病治疗的进展显著提高了缓解率,但疾病复发仍然是一个重大风险。通过利用敏感、非侵入性的成像指导,可加快检测靶向治疗后早期白血病浸润和残留肿瘤负荷的程度,从而实现更有效的治疗计划。我们利用报告基因成像技术和系统性给予 luc+和 GFP+人白血病细胞 (LC) 的小鼠系统,证明了新一代血管破坏剂 combretastatin-A1-diphosphate (OXi4503) 的显著生存获益和治疗效果。在治疗前,连续监测同源双转导细胞的归巢情况,并使用生物发光成像 (BLI) 绘制全身细胞分布图谱。成像结果与实体器官/组织中定量 GFP 表达水平强烈相关,表明测量的 BLI 信号提供了系统白血病模型中肿瘤组织负担的高度敏感和可靠的生物标志物。因此,这种光学技术可以作为临床前药物发现的强大非侵入性成像工具,用于快速筛选有前途的治疗剂,以确定其效力、治疗效果和生存优势。我们进一步表明,GFP+HL-60 细胞与 VE-钙黏蛋白和 CD31 表达的内皮细胞密切相关,提示血管周围龛位可能在 LC 的维持和存活中发挥关键作用。

相似文献

1
Serial monitoring of human systemic and xenograft models of leukemia using a novel vascular disrupting agent.新型血管破坏剂在人类系统性白血病和异种移植模型中的连续监测。
Leukemia. 2012 Aug;26(8):1771-8. doi: 10.1038/leu.2012.48. Epub 2012 Feb 20.
2
Effect of the second-generation vascular disrupting agent OXi4503 on tumor vascularity.第二代血管破坏剂OXi4503对肿瘤血管的影响。
Clin Cancer Res. 2006 Jul 1;12(13):4090-4. doi: 10.1158/1078-0432.CCR-06-0163.
3
Vascular disruptive agent OXi4503 and anti-angiogenic agent Sunitinib combination treatment prolong survival of mice with CRC liver metastasis.血管破坏剂OXi4503与抗血管生成剂舒尼替尼联合治疗可延长结直肠癌肝转移小鼠的生存期。
BMC Cancer. 2016 Jul 26;16:533. doi: 10.1186/s12885-016-2568-7.
4
Vascular targeting agent Oxi4503 inhibits tumor growth in a colorectal liver metastases model.血管靶向剂Oxi4503在结直肠癌肝转移模型中抑制肿瘤生长。
J Gastroenterol Hepatol. 2008 Jul;23(7 Pt 2):e96-e104. doi: 10.1111/j.1440-1746.2007.04899.x. Epub 2007 Jun 7.
5
Oxi4503, a novel vascular targeting agent: effects on blood flow and antitumor activity in comparison to combretastatin A-4 phosphate.Oxi4503,一种新型血管靶向剂:与磷酸考布他汀A-4相比,对血流和抗肿瘤活性的影响。
Anticancer Res. 2003 Mar-Apr;23(2B):1433-40.
6
Low-dose metronomic cyclophosphamide combined with vascular disrupting therapy induces potent antitumor activity in preclinical human tumor xenograft models.低剂量节拍式环磷酰胺联合血管破坏疗法在临床前人源肿瘤异种移植模型中诱导强烈的抗肿瘤活性。
Mol Cancer Ther. 2009 Oct;8(10):2872-81. doi: 10.1158/1535-7163.MCT-09-0583.
7
Support of a free radical mechanism for enhanced antitumor efficacy of the microtubule disruptor OXi4503.支持自由基机制增强微管破坏剂 OXi4503 的抗肿瘤疗效。
Microvasc Res. 2011 Jan;81(1):44-51. doi: 10.1016/j.mvr.2010.10.003. Epub 2010 Oct 23.
8
In vivo imaging enables high resolution preclinical trials on patients' leukemia cells growing in mice.体内成像使在小鼠中生长的患者白血病细胞的高分辨率临床前试验成为可能。
PLoS One. 2012;7(12):e52798. doi: 10.1371/journal.pone.0052798. Epub 2012 Dec 31.
9
Leukemia regression by vascular disruption and antiangiogenic therapy.血管破坏和抗血管生成治疗导致白血病消退。
Blood. 2010 Sep 2;116(9):1539-47. doi: 10.1182/blood-2009-06-230474. Epub 2010 May 14.
10
Dual targeting of tumor vasculature: combining Avastin and vascular disrupting agents (CA4P or OXi4503).肿瘤血管双重靶向治疗:联合使用阿瓦斯汀与血管破坏剂(CA4P或OXi4503)。
Anticancer Res. 2008 Jul-Aug;28(4B):2027-31.

引用本文的文献

1
Analysis of global trends in acute lymphoblastic leukemia in children aged 0-5 years from 1990 to 2021.1990年至2021年0至5岁儿童急性淋巴细胞白血病全球趋势分析。
Front Pediatr. 2025 Mar 13;13:1542649. doi: 10.3389/fped.2025.1542649. eCollection 2025.
2
Bone Marrow Microenvironment as a Source of New Drug Targets for the Treatment of Acute Myeloid Leukaemia.骨髓微环境作为治疗急性髓系白血病新药靶点的来源。
Int J Mol Sci. 2022 Dec 29;24(1):563. doi: 10.3390/ijms24010563.
3
Leukemia stem cell-bone marrow microenvironment interplay in acute myeloid leukemia development.急性髓系白血病发展过程中白血病干细胞与骨髓微环境的相互作用
Exp Hematol Oncol. 2021 Jul 10;10(1):39. doi: 10.1186/s40164-021-00233-2.
4
Therapeutic Targeting of the Leukaemia Microenvironment.白血病微环境的治疗靶点
Int J Mol Sci. 2021 Jun 26;22(13):6888. doi: 10.3390/ijms22136888.
5
Non-Invasive Evaluation of Acute Effects of Tubulin Binding Agents: A Review of Imaging Vascular Disruption in Tumors.微管蛋白结合剂急性效应的非侵入性评估:肿瘤血管破坏成像综述
Molecules. 2021 Apr 27;26(9):2551. doi: 10.3390/molecules26092551.
6
A Phase 1B Clinical Study of Combretastatin A1 Diphosphate (OXi4503) and Cytarabine (ARA-C) in Combination (OXA) for Patients with Relapsed or Refractory Acute Myeloid Leukemia.磷酸二氢柯里拉京(OXi4503)与阿糖胞苷(ARA-C)联合用药(OXA)用于复发或难治性急性髓系白血病患者的1B期临床研究
Cancers (Basel). 2019 Dec 26;12(1):74. doi: 10.3390/cancers12010074.
7
Microtubule destabilising agents: far more than just antimitotic anticancer drugs.微管解聚剂:远不止是抗有丝分裂抗癌药物。
Br J Clin Pharmacol. 2017 Feb;83(2):255-268. doi: 10.1111/bcp.13126. Epub 2016 Oct 18.
8
Preclinical Activity of the Vascular Disrupting Agent OXi4503 against Head and Neck Cancer.血管破坏剂OXi4503对头颈部癌的临床前活性
Cancers (Basel). 2016 Jan 7;8(1):11. doi: 10.3390/cancers8010011.

本文引用的文献

1
Leukemia regression by vascular disruption and antiangiogenic therapy.血管破坏和抗血管生成治疗导致白血病消退。
Blood. 2010 Sep 2;116(9):1539-47. doi: 10.1182/blood-2009-06-230474. Epub 2010 May 14.
2
In vivo functional differences in microvascular response of 4T1 and Caki-1 tumors after treatment with OXi4503.经 OXi4503 治疗后,4T1 和 Caki-1 肿瘤的微血管反应的体内功能差异。
Oncol Rep. 2010 Mar;23(3):685-92. doi: 10.3892/or_00000685.
3
Low-dose metronomic cyclophosphamide combined with vascular disrupting therapy induces potent antitumor activity in preclinical human tumor xenograft models.低剂量节拍式环磷酰胺联合血管破坏疗法在临床前人源肿瘤异种移植模型中诱导强烈的抗肿瘤活性。
Mol Cancer Ther. 2009 Oct;8(10):2872-81. doi: 10.1158/1535-7163.MCT-09-0583.
4
Acute vascular disruption by 5,6-dimethylxanthenone-4-acetic Acid in an orthotopic model of human head and neck cancer.5,6-二甲基黄嘌呤-4-乙酸在人头颈癌原位模型中的急性血管破坏作用。
Transl Oncol. 2009 Aug 18;2(3):121-7. doi: 10.1593/tlo.09103.
5
New therapeutic strategies in acute lymphoblastic leukemia.急性淋巴细胞白血病的新治疗策略
Semin Hematol. 2009 Jan;46(1):76-88. doi: 10.1053/j.seminhematol.2008.09.009.
6
Bioluminescent evaluation of the therapeutic effects of total body irradiation in a murine hematological malignancy model.在小鼠血液系统恶性肿瘤模型中对全身照射治疗效果的生物发光评估。
Exp Hematol. 2008 Dec;36(12):1634-41. doi: 10.1016/j.exphem.2008.08.004. Epub 2008 Oct 25.
7
Dual targeting of tumor vasculature: combining Avastin and vascular disrupting agents (CA4P or OXi4503).肿瘤血管双重靶向治疗:联合使用阿瓦斯汀与血管破坏剂(CA4P或OXi4503)。
Anticancer Res. 2008 Jul-Aug;28(4B):2027-31.
8
Antineoplastic agents. 552. Oxidation of combretastatin A-1: trapping the o-quinone intermediate considered the metabolic product of the corresponding phosphate prodrug.抗肿瘤药。552. 柯桠素A-1的氧化:捕获被认为是相应磷酸前体药物代谢产物的邻醌中间体。
J Nat Prod. 2008 Sep;71(9):1561-3. doi: 10.1021/np800179g. Epub 2008 Aug 27.
9
Human acute leukemia cells injected in NOD/LtSz-scid/IL-2Rgamma null mice generate a faster and more efficient disease compared to other NOD/scid-related strains.与其他NOD/scid相关品系相比,将人类急性白血病细胞注射到NOD/LtSz-scid/IL-2Rγ基因敲除小鼠中会产生更快且更有效的疾病。
Int J Cancer. 2008 Nov 1;123(9):2222-7. doi: 10.1002/ijc.23772.
10
Antivascular effects of combretastatin A4 phosphate in breast cancer xenograft assessed using dynamic bioluminescence imaging and confirmed by MRI.使用动态生物发光成像评估并经磁共振成像证实的磷酸考布他汀A4对乳腺癌异种移植瘤的抗血管生成作用
FASEB J. 2008 Jul;22(7):2445-51. doi: 10.1096/fj.07-103713. Epub 2008 Feb 8.