Suppr超能文献

中和性抗血管内皮生长因子抗体在体内可完全抑制人前列腺癌微肿瘤的血管生成和生长。

Neutralizing anti-vascular endothelial growth factor antibody completely inhibits angiogenesis and growth of human prostate carcinoma micro tumors in vivo.

作者信息

Borgström P, Bourdon M A, Hillan K J, Sriramarao P, Ferrara N

机构信息

Sidney Kimmel Cancer Center, San Diego, California 92121, USA.

出版信息

Prostate. 1998 Apr 1;35(1):1-10. doi: 10.1002/(sici)1097-0045(19980401)35:1<1::aid-pros1>3.0.co;2-o.

Abstract

BACKGROUND

Neovascularization mediated by growth factors produced by tumors is critical for the growth of tumors. Vascular endothelial growth factor (VEGF) is one such growth factor. A neutralizing anti-VEGF antibody (A4.6.1) was recently shown in vivo to inhibit tumor angiogenesis and growth of the human rhabdomyosarcoma cell line A673. The antibody profoundly changed the growth characteristics of the tumor line from a rapidly growing malignancy to a dormant microcolony.

METHODS

In the present study, we evaluated the effects of A4.6.1 (100 microg twice weekly, i.p.) on growth and angiogenic activity of spheroids of the human prostatic cell line DU 145 (diameter 700 microm at implantation) implanted in dorsal skinfold chambers in nude mice (n = 11). An antibody of the same isotype (n = 5) or saline (n = 5) was used as control. Tumor cells were prelabeled with a fluorescent vital dye (CMTMR), which allowed measurement of size of the implanted tumor spheroids throughout a two week observation period. FITC-dextran was used for plasma enhancement to visualize angiogenic activity.

RESULTS

Tumors of control animals induced a neo-vasculature with high vascular density (350+/-12 cm[-1]). In animals treated with the anti-VEGF antibody, there was complete inhibition of neovascularization of the micro tumors and complete inhibition of tumor growth after the initial prevascular angiogenesis independent growth phase.

CONCLUSIONS

These results demonstrate that inhibition of the key regulatory paracrine growth factor for endothelial cells, VEGF, results in complete suppression of prostate cancer induced angiogenesis and prevents tumor growth beyond the initial prevascular growth phase.

摘要

背景

肿瘤产生的生长因子介导的新血管生成对肿瘤生长至关重要。血管内皮生长因子(VEGF)就是这样一种生长因子。最近在体内研究显示,一种中和性抗VEGF抗体(A4.6.1)可抑制人横纹肌肉瘤细胞系A673的肿瘤血管生成和生长。该抗体使肿瘤细胞系的生长特性从快速生长的恶性肿瘤深刻转变为休眠的微菌落。

方法

在本研究中,我们评估了A4.6.1(每周两次,腹腔注射100微克)对植入裸鼠背部皮褶小室的人前列腺细胞系DU 145球体(植入时直径700微米)生长和血管生成活性的影响。使用相同同种型的抗体(n = 5)或生理盐水(n = 5)作为对照。肿瘤细胞用荧光活性染料(CMTMR)预先标记,这使得在两周的观察期内能够测量植入肿瘤球体的大小。使用异硫氰酸荧光素 - 葡聚糖进行血浆增强以可视化血管生成活性。

结果

对照动物的肿瘤诱导出具有高血管密度(350±12 cm[-1])的新血管系统。在用抗VEGF抗体治疗的动物中,微肿瘤的新血管生成完全受到抑制,并且在初始的血管生成前独立生长阶段之后肿瘤生长完全受到抑制。

结论

这些结果表明,抑制内皮细胞的关键调节旁分泌生长因子VEGF会导致前列腺癌诱导的血管生成完全受到抑制,并防止肿瘤在初始血管生成前生长阶段之后继续生长。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验