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Cancer Res ; 78(12): 3233-3242, 2018 06 15.
Article in English | MEDLINE | ID: mdl-29661830

ABSTRACT

Mounting clinical and preclinical evidence supports a key role for sustained adrenergic signaling in the tumor microenvironment as a driver of tumor growth and progression. However, the mechanisms by which adrenergic neurotransmitters are delivered to the tumor microenvironment are not well understood. Here we present evidence for a feed-forward loop whereby adrenergic signaling leads to increased tumoral innervation. In response to catecholamines, tumor cells produced brain-derived neurotrophic factor (BDNF) in an ADRB3/cAMP/Epac/JNK-dependent manner. Elevated BDNF levels in the tumor microenvironment increased innervation by signaling through host neurotrophic receptor tyrosine kinase 2 receptors. In patients with cancer, high tumor nerve counts were significantly associated with increased BDNF and norepinephrine levels and decreased overall survival. Collectively, these data describe a novel pathway for tumor innervation, with resultant biological and clinical implications.Significance: Sustained adrenergic signaling promotes tumor growth and metastasis through BDNF-mediated tumoral innervation. Cancer Res; 78(12); 3233-42. ©2018 AACR.


Subject(s)
Brain-Derived Neurotrophic Factor/metabolism , Feedback, Physiological , Neoplasms/pathology , Norepinephrine/metabolism , Receptors, Adrenergic, beta-3/metabolism , Animals , Cell Line, Tumor , Cyclic AMP/metabolism , Female , Guanine Nucleotide Exchange Factors/metabolism , Humans , Membrane Glycoproteins/metabolism , Mice , Neoplasms/mortality , Peripheral Nerves/metabolism , Peripheral Nerves/pathology , Receptor, trkB/metabolism , Signal Transduction , Tumor Microenvironment/physiology , Xenograft Model Antitumor Assays
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