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MCF-7乳腺癌细胞中血管内皮生长因子的过表达促进体内雌激素非依赖性肿瘤生长。

Overexpression of vascular endothelial growth factor by MCF-7 breast cancer cells promotes estrogen-independent tumor growth in vivo.

作者信息

Guo Ping, Fang Quan, Tao Huo-Quan, Schafer Christopher A, Fenton Bruce M, Ding Ivan, Hu Bo, Cheng Shi-Yuan

机构信息

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.

出版信息

Cancer Res. 2003 Aug 1;63(15):4684-91.

Abstract

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.

摘要

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。

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