Autonomic Nerve Development Contributes to Prostate Cancer Progression

被引:933
作者
Magnon, Claire [1 ,2 ,3 ]
Hall, Simon J. [4 ]
Lin, Juan [5 ]
Xue, Xiaonan [5 ]
Gerber, Leah [6 ,7 ]
Freedland, Stephen J. [6 ,7 ,8 ]
Frenette, Paul S. [1 ,2 ,3 ]
机构
[1] Albert Einstein Coll Med, Ruth L & David S Gottesman Inst Stem Cell & Regen, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
[3] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10461 USA
[4] Mt Sinai Sch Med, Dept Urol, New York, NY 10029 USA
[5] Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10461 USA
[6] Durham VA Med Ctr, Dept Surg, Durham, NC 27705 USA
[7] Duke Univ, Dept Surg, Div Urol, Durham, NC 27705 USA
[8] Duke Univ, Dept Pathol, Durham, NC 27705 USA
关键词
BEAM RADIATION-THERAPY; PERINEURAL INVASION; RADICAL PROSTATECTOMY; BETA-BLOCKERS; CHOLINERGIC INNERVATION; MUSCARINIC RECEPTORS; BREAST-CANCER; TUMOR-GROWTH; SURVIVAL; CELLS;
D O I
10.1126/science.1236361
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nerves are a common feature of the microenvironment, but their role in tumor growth and progression remains unclear. We found that the formation of autonomic nerve fibers in the prostate gland regulates prostate cancer development and dissemination in mouse models. The early phases of tumor development were prevented by chemical or surgical sympathectomy and by genetic deletion of stromal beta(2)- and beta(3)-adrenergic receptors. Tumors were also infiltrated by parasympathetic cholinergic fibers that promoted cancer dissemination. Cholinergic-induced tumor invasion and metastasis were inhibited by pharmacological blockade or genetic disruption of the stromal type 1 muscarinic receptor, leading to improved survival of the mice. A retrospective blinded analysis of prostate adenocarcinoma specimens from 43 patients revealed that the densities of sympathetic and parasympathetic nerve fibers in tumor and surrounding normal tissue, respectively, were associated with poor clinical outcomes. These findings may lead to novel therapeutic approaches for prostate cancer.
引用
收藏
页码:143 / +
页数:11
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