血管生成拟态
血管生成
内化
医学
乳腺癌
病理
癌症研究
灌注
癌症
化学
内科学
转移
受体
作者
Hisataka Kobayashi,Kazuo Shirakawa,Satomi Kawamoto,Tsuneo Saga,Noriko Sato,Akira Hiraga,Ichiro Watanabe,Yuji Heike,Kaori Togashi,Junji Konishi,Martin W. Brechbiel,Hiro Wakasugi
出处
期刊:PubMed
日期:2002-02-01
卷期号:62 (3): 860-6
被引量:95
摘要
The rapid blood flow and perfusion of macromolecules in the inflammatory breast cancer xenograft (WIBC-9), which exhibits a "vasculogenic mimicry" type of angiogenesis without the participation of endothelial cells and expresses high levels of the HER-2/neu antigen, was evaluated in mice using 3D-micro-MR angiography using a novel macromolecular MR contrast agent [G6-(1B4M-Gd)(256)]. Herceptin, which recognizes the HER-2/neu antigen and has similar size (10 nm) to G6-(1B4M-Gd)(256), accumulated and internalized in the WIBC-9 tumors more quickly than in the control MC-5 tumors that progress with normal angiogenesis. Three dimensional micro-MRI with the G6-(1B4M-Gd)(256) macromolecular MRI contrast agent distinguishes between the different types of angiogenesis and is predictive of the rapid accumulation and internalization of Herceptin in the WIBC-9 inflammatory breast cancer xenograft.
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