• 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

The preclinical evaluation of angiogenesis inhibitors.

作者信息

O'Reilly M S

机构信息

Department of Surgery, Children's Hospital, Boston, MA, USA.

出版信息

Invest New Drugs. 1997;15(1):5-13. doi: 10.1023/a:1005762410476.

DOI:10.1023/a:1005762410476
PMID:9195285
Abstract

Angiogenesis is a fundamental process which is required for a number of physiological and pathophysiological processes. The field of angiogenesis therefore has many therapeutic implications and has progressed rapidly. Many strategies have been devised to regulate angiogenesis and several endogenous and synthetic inhibitors of angiogenesis have now been identified. These inhibitors can be used to treat a number of angiogenesis-dependent diseases and they offer a novel means of potently inhibiting tumor growth without significant toxicity or drug resistance. Recently, some of these inhibitors have entered clinical trials. In this article, I will review methods currently employed in the preclinical evaluation of angiogenesis inhibitors and I will discuss some of the implications of angiogenesis research.

摘要

相似文献

1
The preclinical evaluation of angiogenesis inhibitors.
Invest New Drugs. 1997;15(1):5-13. doi: 10.1023/a:1005762410476.
2
An overview of clinical trials involving inhibitors of angiogenesis and their mechanism of action.涉及血管生成抑制剂的临床试验概述及其作用机制。
Invest New Drugs. 1997;15(1):49-59. doi: 10.1023/a:1005770612294.
3
Suppression of angiogenesis, tumor growth, and wound healing by resveratrol, a natural compound in red wine and grapes.白藜芦醇(一种红酒和葡萄中的天然化合物)对血管生成、肿瘤生长和伤口愈合的抑制作用。
FASEB J. 2001 Aug;15(10):1798-800. doi: 10.1096/fj.01-0028fje.
4
Chorioallantoic membrane capillary bed: a useful target for studying angiogenesis and anti-angiogenesis in vivo.绒毛尿囊膜毛细血管床:体内研究血管生成和抗血管生成的有用靶点。
Anat Rec. 2001 Dec 1;264(4):317-24. doi: 10.1002/ar.10021.
5
Anti-angiogenic activities of Cnidium officinale Makino and Tabanus bovinus.日本芎䓖和牛虻的抗血管生成活性。
J Ethnopharmacol. 2002 Aug;81(3):373-9. doi: 10.1016/s0378-8741(02)00122-8.
6
Inhibition of angiogenesis by humulone, a bitter acid from beer hop.啤酒花中的苦味酸蛇麻酮对血管生成的抑制作用。
Biochem Biophys Res Commun. 2001 Nov 23;289(1):220-4. doi: 10.1006/bbrc.2001.5934.
7
Purine analogue 6-methylmercaptopurine riboside inhibits early and late phases of the angiogenesis process.嘌呤类似物6-甲基巯基嘌呤核苷可抑制血管生成过程的早期和晚期阶段。
Cancer Res. 1999 May 15;59(10):2417-24.
8
Inhibition of angiogenesis and tumor growth by SCH221153, a dual alpha(v)beta3 and alpha(v)beta5 integrin receptor antagonist.双α(v)β3和α(v)β5整合素受体拮抗剂SCH221153对血管生成和肿瘤生长的抑制作用
Cancer Res. 2001 Mar 1;61(5):2232-8.
9
Angiogenesis assays in the chick CAM.鸡胚绒毛尿囊膜血管生成实验
Methods Mol Biol. 2005;294:123-36. doi: 10.1385/1-59259-860-9:123.
10
Anti-angiogenic activity of the purine analog 6-thioguanine.嘌呤类似物6-硫鸟嘌呤的抗血管生成活性。
Leukemia. 2002 Aug;16(8):1490-9. doi: 10.1038/sj.leu.2402646.

引用本文的文献

1
Arterial Spin Labeled Perfusion MRI for the Evaluation of Response to Tyrosine Kinase Inhibition Therapy in Metastatic Renal Cell Carcinoma.动脉自旋标记灌注 MRI 评估转移性肾细胞癌酪氨酸激酶抑制治疗的反应。
Radiology. 2021 Feb;298(2):332-340. doi: 10.1148/radiol.2020201763. Epub 2020 Dec 1.
2
A novel polysaccharide from Sargassum integerrimum induces apoptosis in A549 cells and prevents angiogensis in vitro and in vivo.一种来自全缘马尾藻的新型多糖可诱导A549细胞凋亡,并在体内外抑制血管生成。
Sci Rep. 2016 May 24;6:26722. doi: 10.1038/srep26722.
3
From nutraceuticals to pharmaceuticals to nanopharmaceuticals: a case study in angiogenesis modulation during oxidative stress.

本文引用的文献

1
Antiangiogenic therapy of transgenic mice impairs de novo tumor growth.对转基因小鼠进行抗血管生成治疗会损害肿瘤的新生生长。
Proc Natl Acad Sci U S A. 1996 Mar 5;93(5):2002-7. doi: 10.1073/pnas.93.5.2002.
2
A model of angiogenesis in the mouse cornea.小鼠角膜血管生成模型。
Invest Ophthalmol Vis Sci. 1996 Jul;37(8):1625-32.
3
Angiostatin induces and sustains dormancy of human primary tumors in mice.血管抑素可诱导并维持小鼠体内人原发性肿瘤的休眠状态。
从营养保健品到药物再到纳米药物:氧化应激期间血管生成调节的一个案例研究。
Mol Biotechnol. 2007 Sep;37(1):72-80. doi: 10.1007/s12033-007-0064-7.
4
Current approaches and future strategies for pancreatic carcinoma.
Invest New Drugs. 2000 Feb;18(1):43-56. doi: 10.1023/a:1006383831045.
5
The rationale and future potential of angiogenesis inhibitors in neoplasia.肿瘤血管生成抑制剂的原理及未来潜力
Drugs. 1999 Jul;58(1):17-38. doi: 10.2165/00003495-199958010-00003.
Nat Med. 1996 Jun;2(6):689-92. doi: 10.1038/nm0696-689.
4
Tumor angiogenesis and tissue factor.肿瘤血管生成与组织因子
Nat Med. 1996 Feb;2(2):167-8. doi: 10.1038/nm0296-167.
5
Elevated levels of the angiogenic peptide basic fibroblast growth factor in urine of bladder cancer patients.膀胱癌患者尿液中血管生成肽碱性成纤维细胞生长因子水平升高。
J Natl Cancer Inst. 1993 Feb 3;85(3):241-2. doi: 10.1093/jnci/85.3.241.
6
Synergistic effects of vascular endothelial growth factor and basic fibroblast growth factor on the proliferation and cord formation of bovine capillary endothelial cells within collagen gels.血管内皮生长因子和碱性成纤维细胞生长因子对胶原凝胶内牛毛细血管内皮细胞增殖和条索形成的协同作用。
Lab Invest. 1993 Nov;69(5):508-17.
7
Interferons alpha and beta down-regulate the expression of basic fibroblast growth factor in human carcinomas.
Proc Natl Acad Sci U S A. 1995 May 9;92(10):4562-6. doi: 10.1073/pnas.92.10.4562.
8
The 16-kilodalton N-terminal fragment of human prolactin is a potent inhibitor of angiogenesis.人催乳素16千道尔顿的N端片段是血管生成的强效抑制剂。
Endocrinology. 1993 Sep;133(3):1292-9. doi: 10.1210/endo.133.3.7689950.
9
Peptides derived from two separate domains of the matrix protein thrombospondin-1 have anti-angiogenic activity.源自基质蛋白血小板反应蛋白-1两个不同结构域的肽具有抗血管生成活性。
J Cell Biol. 1993 Jul;122(2):497-511. doi: 10.1083/jcb.122.2.497.
10
Analysis of experimental antiangiogenic therapy.实验性抗血管生成疗法分析
J Pediatr Surg. 1993 Mar;28(3):445-50; discussion 450-1. doi: 10.1016/0022-3468(93)90246-h.