Guo Ping, Fang Quan, Tao Huo-Quan, Schafer Christopher A, Fenton Bruce M, Ding Ivan, Hu Bo, Cheng Shi-Yuan
University of Pittsburgh Cancer Institute and Department of Pathology, Research Pavilion at Hillman Cancer Center, Suite 2.26, 5117 Centre Avenue, Pittsburgh, PA 15213-1863, USA.
Cancer Res. 2003 Aug 1;63(15):4684-91.
Alteration of the phenotype of breast cancers from estrogen-dependent to estrogen-independent growth often leads to the failure of antiestrogenic tumor therapies. We report that overexpression of vascular endothelial growth factor (VEGF) by estrogen-dependent MCF-7 breast cancer cells could abolish estrogen-dependent tumor growth in ovariectomized mice. In the absence of estrogen, MCF-7 VEGF-expressing tumors with increased vessel density showed growth kinetics similar to, or even greater than, that of parental MCF-7 tumors with estrogen supplementation. Overexpression of VEGF by MCF-7 cells or treatment on parental MCF-7 cells with recombinant VEGF also stimulated cell proliferation in culture. Our data suggest that VEGF stimulation of MCF-7 tumor angiogenesis and growth is mediated by both autocrine and paracrine mechanisms.
乳腺癌的表型从雌激素依赖型生长转变为雌激素非依赖型生长,常常导致抗雌激素肿瘤治疗失败。我们报告称,雌激素依赖型MCF-7乳腺癌细胞中血管内皮生长因子(VEGF)的过表达能够消除去卵巢小鼠中雌激素依赖型肿瘤的生长。在没有雌激素的情况下,血管密度增加的MCF-7 VEGF表达肿瘤的生长动力学与补充雌激素的亲代MCF-7肿瘤相似,甚至更强。MCF-7细胞VEGF的过表达或用重组VEGF处理亲代MCF-7细胞也能在培养中刺激细胞增殖。我们的数据表明,VEGF对MCF-7肿瘤血管生成和生长的刺激是由自分泌和旁分泌机制介导的。