Rowe D H, Kayton M L, O'Toole K M, Ingram M, Stolar C J, Kandel J J
Division of Pediatric Surgery, College of Physicians and Surgeons, Columbia University and Babies and Children's Hospital of New York, NY 10032, USA.
J Pediatr Surg. 1999 May;34(5):676-9. doi: 10.1016/s0022-3468(99)90354-8.
BACKGROUND/PURPOSE: Pathological vascular architecture is a feature of neoangiogenic processes such as diseases of the retina and tumor growth. The authors hypothesized that experimental human Wilms' tumors would display a vascular architecture similar to retinal diseases that are driven by vascular endothelial growth factor (VEGF).
Human Wilms' tumors were established in the right kidneys of nude mice. After 4.5 weeks of tumor growth, fluorescein angiograms were performed before death. Representative sections of tumors and contralateral, control kidneys were evaluated by fluorescent microscopy.
Fluorescein angiograms demonstrated a characteristic pathological architecture. Vascular tortuosity, capillary tufting, and hemorrhage were noted. These features were not present in normal kidneys.
Vascular architecture of Wilms' tumor displays the specific features previously described in diseases of the retina, which have been shown to be driven by VEGF, suggesting that neoangiogenesis in this model is also VEGF driven.
背景/目的:病理性血管结构是新生血管生成过程的一个特征,如视网膜疾病和肿瘤生长。作者推测,实验性人类肾母细胞瘤将表现出与由血管内皮生长因子(VEGF)驱动的视网膜疾病相似的血管结构。
将人类肾母细胞瘤接种于裸鼠右肾。肿瘤生长4.5周后,在处死前进行荧光血管造影。通过荧光显微镜对肿瘤和对侧对照肾脏的代表性切片进行评估。
荧光血管造影显示出特征性的病理结构。观察到血管迂曲、毛细血管簇状增生和出血。这些特征在正常肾脏中不存在。
肾母细胞瘤的血管结构显示出先前在视网膜疾病中描述的特定特征,这些特征已被证明是由VEGF驱动的,这表明该模型中的新生血管生成也是由VEGF驱动的。