血管生成
前列腺癌
癌症研究
前列腺
癌症
受体
内皮干细胞
内分泌学
基质
内皮
生物
细胞生物学
医学
内科学
生物化学
体外
免疫组织化学
作者
Ali H. Zahalka,Anna Arnal Estape,Maria Maryanovich,Fumio Nakahara,Cristian D. Cruz,Lydia W.S. Finley,Paul S. Frenette
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2017-10-19
卷期号:358 (6361): 321-326
被引量:357
标识
DOI:10.1126/science.aah5072
摘要
Tumor angiogenesis gets nervous The microenvironment of solid tumors hosts many intercellular conversations that can either enhance or inhibit tumor growth. Interestingly, the tumor cells need not be direct participants in these conversations. Zahalka et al. studied genetically manipulated mouse models and found that adrenergic signals from autonomic nerves in the prostate cancer microenvironment fueled tumor growth by altering the metabolism of blood vessel endothelial cells (see the Perspective by Hayakawa and Wang). These nerve-derived signals suppressed oxidative phosphorylation in the endothelial cells, activating an angiogenic switch that facilitated rapid tumor growth. This cross-talk between nerves and endothelial cells could potentially offer a target for cancer therapies. Science , this issue p. 321 ; see also p. 305
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