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本文引用的文献

1
Targeting tumour vasculature: the development of combretastatin A4.靶向肿瘤血管:康普瑞汀A4的研发
Lancet Oncol. 2001 Feb;2(2):82-7. doi: 10.1016/S1470-2045(00)00224-2.
2
In vivo and in vitro evaluation of combretastatin A-4 and its sodium phosphate prodrug.秋水仙素 A-4 及其磷酸钠前药的体内和体外评价。
Br J Cancer. 1999 Dec;81(8):1318-27. doi: 10.1038/sj.bjc.6692174.
3
Antineoplastic agents 393. Synthesis of the trans-isomer of combretastatin A-4 prodrug.抗肿瘤药393. 康普瑞他汀A-4前药反式异构体的合成。
Anticancer Drug Des. 1998 Dec;13(8):981-93.
4
Combretastatin A-4 phosphate as a tumor vascular-targeting agent: early effects in tumors and normal tissues.磷酸考布他汀A-4作为一种肿瘤血管靶向剂:对肿瘤和正常组织的早期作用
Cancer Res. 1999 Apr 1;59(7):1626-34.
5
Growth factors and goitrogenesis.生长因子与甲状腺肿形成
J Endocrinol. 1999 Mar;160(3):321-32. doi: 10.1677/joe.0.1600321.
6
Magnetic resonance imaging and spectroscopy of combretastatin A4 prodrug-induced disruption of tumour perfusion and energetic status.康普瑞他汀A4前药诱导的肿瘤灌注和能量状态破坏的磁共振成像与波谱分析
Br J Cancer. 1998 Jun;77(11):1761-7. doi: 10.1038/bjc.1998.294.
7
Presence and possible role of vascular endothelial growth factor in thyroid cell growth and function.
J Endocrinol. 1998 Apr;157(1):5-12. doi: 10.1677/joe.0.1570005.
8
Antineoplastic agents 389. New syntheses of the combretastatin A-4 prodrug.抗肿瘤药389. 康普他汀A - 4前药的新合成方法。
Anticancer Drug Des. 1998 Apr;13(3):183-91.
9
Upregulation of the angiogenic factors PlGF, VEGF and their receptors (Flt-1, Flk-1/KDR) by TSH in cultured thyrocytes and in the thyroid gland of thiouracil-fed rats suggest a TSH-dependent paracrine mechanism for goiter hypervascularization.促甲状腺激素(TSH)在培养的甲状腺细胞以及用硫脲嘧啶喂养的大鼠甲状腺中上调血管生成因子胎盘生长因子(PlGF)、血管内皮生长因子(VEGF)及其受体(Flt-1、Flk-1/KDR),提示存在一种TSH依赖性旁分泌机制参与甲状腺肿的血管过度增生。
Oncogene. 1997 Nov 27;15(22):2687-98. doi: 10.1038/sj.onc.1201456.
10
Synthesis of biologically active polyphenolic glycosides (combretastatin and resveratrol series).
Carbohydr Res. 1997 Jun 20;301(3-4):95-109. doi: 10.1016/s0008-6215(97)00087-6.

康普瑞他汀 - A4破坏非肿瘤组织中的新血管形成。

Combretastatin-A4 disrupts neovascular development in non-neoplastic tissue.

作者信息

Griggs J, Hesketh R, Smith G A, Brindle K M, Metcalfe J C, Thomas G A, Williams E D

机构信息

Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge CB2 1QW, UK.

出版信息

Br J Cancer. 2001 Mar 23;84(6):832-5. doi: 10.1054/bjoc.2000.1653.

DOI:10.1054/bjoc.2000.1653
PMID:11259100
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2363811/
Abstract

Combretastatin-A4 phosphate (cis-CA-4) is a tubulin-binding agent currently undergoing clinical trials as an anti-tumour drug. We have investigated whether CA-4 functions as a tumour-specific anti-vascular agent using the hyperplastic thyroid as a novel in vivo model of neovascularization. CA-4 elicited pathological changes in normal tissue, manifested as the induction of multiple, discrete intravascular thrombi. These vascular-damaging effects indicate that CA-4P does not function as a tumour-specific agent but targets neovasculature irrespective of the primary angiogenic stimulus.

摘要

磷酸考布他汀 - A4(顺式 - CA - 4)是一种微管结合剂,目前正作为一种抗肿瘤药物进行临床试验。我们利用增生性甲状腺作为新生血管形成的新型体内模型,研究了CA - 4是否作为一种肿瘤特异性抗血管生成剂发挥作用。CA - 4在正常组织中引发了病理变化,表现为多个离散的血管内血栓形成。这些血管损伤效应表明,CA - 4P并非作为一种肿瘤特异性药物发挥作用,而是不论主要血管生成刺激因素如何,均靶向新生血管。