血管生成
转染
基质凝胶
癌症研究
腺癌
细胞生长
化学
生物
细胞培养
癌症
分子生物学
内科学
医学
生物化学
遗传学
作者
Daotai Nie,Gilda G. Hillman,Timothy J. Geddes,Keqin Tang,Christopher R. Pierson,David J. Grignon,Kenneth V. Honn
出处
期刊:PubMed
日期:1998-09-15
卷期号:58 (18): 4047-51
被引量:97
摘要
Previously, we found a positive correlation between the expression of platelet-type 12-lipoxygenase (12-LOX) and the progression of human prostate adenocarcinoma (PCa; Gao et al., Urology, 46: 227-237, 1995). To determine the role of 12-LOX in PCa progression, we generated stable 12-LOX-transfected PC3 cells, which synthesize high levels of 12-LOX protein and 12(S)-hydroxyeicosatetraenoic acid metabolite. In vitro, 12-LOX-transfected PC3 cells demonstrated a proliferation rate similar to neo controls. However, following s.c. injection into athymic nude mice, 12-LOX-transfected PC3 cells formed larger tumors than did the controls. Decreased necrosis and increased vascularization were observed in the tumors from 12-LOX-transfected PC3 cells. Both endothelial cell migration and Matrigel implantation assays indicate that 12-LOX-transfected PC3 cells were more angiogenic than their neo controls. These data indicate that 12-LOX stimulates human PCa tumor growth by a novel angiogenic mechanism.
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